Abstract

Förster resonance energy transfer (FRET) and Auger recombination in quantum dots (QDs)-molecules system are important mechanisms for affecting performance of their optoelectronic and photosynthesis devices. However, exploring an effective strategy to promote FRET and suppress Auger recombination simultaneously remains a daunting challenge. Here, we report that FRET process is promoted and Auger recombination process is suppressed in CdTe/CdS QDs-Rhodamine101 (Rh101) molecules system upon compression. The greatly improved FRET is attributed to the shortened donor-acceptor distance and increased the number of molecules attached to QDs induced by pressure. The reduced Auger recombination is ascribed to the formation of an alloy layer at the core/shell interface. The FRET can occur 70 times faster than Auger recombination under a high pressure of 0.9 GPa. Our findings demonstrate that high pressure is a robust tool to boost FRET and simultaneously suppress Auger recombination, and provides a new route to QDs-molecules applications.

© 2021 Optical Society of America under the terms of the OSA Open Access Publishing Agreement

1. Introduction

Quantum dots (QDs)-molecules system has been a focus of intense research in the past two decades for applications ranging from light-emitting diodes (LEDs) and optical amplifiers to lasing, photovoltaics and solar energy conversion [13]. For the development and optimization of such applications, it is crucial to understand the photophysics and photochemistry of dynamic process [411], particularly fluorescence resonance energy transfer (FRET) and Auger recombination [1214]. The FRET process has been shown to effectively enhance the performance of light-sensing and -harvesting functions [1516]. In contrast to FRET process, the Auger recombination process loses energy in the form of heat, and is responsible for efficiency roll-off at QD-based applications [1720]. Thus, fast FRET process, coupled with the slow Auger recombination process, are the crucial events associated with the efficiency and functionality of applications.

In recent years, significant efforts have been made in developing efficient approach to accelerate FRET process [21,22] and suppress the unwanted Auger recombination [23,24]. According to the Förster theory, the FRET requires an appreciable spectral overlap of acceptor absorption and the donor emission spectra, and is highly sensitive to the donor–acceptor separation distance and the number of adsorbed acceptor per QD [25,26]. Prior studies suggested that the FRET rate would be enhanced by varying the length of the linker molecule (bridge), assembling multiple acceptors on the surface of the QDs, or increasing acceptor concentration [2731]. For suppressing Auger recombination of QDs, efficient ways are to increase the core volume or to smooth the confinement potential between core and shell materials [12,3233]. Other approach such as engineering alloyed core-shell interface in the QDs has also been proposed to suppress Auger recombination [23,34]. The above results show that the FRET process can be well promoted, and Auger recombination can be effectively inhibited, respectively. However, up to date, simultaneously accelerating FRET process and suppressing the unwanted Auger recombination have not been achieved, which impedes applications of carrier-muliplication-enhanced photovoltaics and electrically pumped lasers [19,35]. Thus, developing a new strategy to simultaneously improve FRET and suppress Auger recombination in QDs-molecules system remains urgent.

Here, we present a new strategy to simultaneously facilitate the FRET process and suppress Auger recombination in the CdTe/CdS QDs-rhodamine101 (Rh101) molecules system by a facile high-pressure tool. By compressing the system from 1atm to 0.9Gpa, pressure shortened the donor-acceptor distance and increased the number of molecules attached to QDs, enhancing the FRET rate dramatically. Meanwhile, the strengthened formation of the alloy layer at core/shell interface of QDs upon compression lead the Auger recombination rate decrease rapidly. The femtosecond transient absorption (TA) experiments [3638] reveal that the FRET rate is 7.1${\times} $ 109 S-1 under atmospheric pressure (1atm) and 1.7${\times} $ 1011 S-1 as pressure increasing to 0.9GPa. The FRET rate can be accelerated for over 20 orders of magnitude. Meanwhile, the Auger recombination rate can be decreased 2-fold simultaneously. Furthermore, the FRET process occurs 70 times faster than Auger recombination process at 0.9GPa. The FRET with a rate that exceeds Auger recombination process, suggest a great progress in fundamental science and in applied fields, including the development of efficient LEDs and reduced threshold optical gain media [39].

2. Experimental details

2.1 Materials

CdTe/CdS QDs and Rh101 molecules were purchased from Xingzi New Material (China) and Sigma (America) without further purification, respectively. The QDs-Rh101 complexes were obtained through adding Rh101 into QDs in aqueous solution. The QDs donor and Rh101 acceptor were solved in water to a concentration of 1 × 10−6 M and 5 × 10−6 M respectively. The surface ligand on the QDs is the 3-mercaptopropionic acid, which makes QDs dissolve well in water.

2.2 High-pressure generation

The diamond anvil cell (DAC) was carried out to generate pressure. The sample and ruby were packed into a DAC chamber with 800 μm diameter, constructed from a T301 steel gasket with a thickness of 100 μm. Then a hole with 500 μm diameter was drilled in center of the indentation by the laser drilling machine. The pressure values were calibrated by the standard ruby fluorescent technique.

2.3 Spectroscopic measurements

The absorption spectra of the CdTe/CdS QDs and Rh101 molecule were obtained on the UV 2550 UV-vis spectrophotometer. The steady-state emission spectra of the CdTe/CdS QDs and QDs-Rh101 complexes were measured by the RF5301 fluorescence spectrophotometer. The femtosecond TA measurements were carried out via a power of 4 W at a 1 kHz repetition rate and 50 fs pulse width. The 400 nm pump pulse (3.1 eV pulse) were generated by Coherent Legend (50 fs, 1 kHz, 800 nm) regenerative amplifier with a BBO crystal. The excitation energy of the sample resolved pump pulses attenuation to 4 μJ. The white light continuum probe pulse was used to generate by a sapphire plate (HELIOS, Ultrafast Systems, United States). The pump pulse and probe pulse were combined in a spectrometer (HELIOS). The kinetic traces were fitted by using Surface Xplorer 2.2 Ultrafast Systems.

3. Results and discussion

Satisfying the basic requirement for the occurrence of FRET process, there is a good spectral overlap between CdTe/CdS QDs fluorescence and Rh101 molecules absorption in aqueous solution (Fig. 1(a)). The transmission electron microscope image of QDs is shown in Fig. S1 of Supplement 1. The absorption spectrum of QDs-Rh101 complexes is shown in Fig. 1(b). Then, we measured the fluorescence spectrum of QDs-Rh101 complexes in aqueous solution. Table S1 shows the emission intensity of QDs alone and QDs in the presence of Rh101 at different pressures. The addition of Rh101 causes a quenching in the fluorescence intensity of QDs. When compressing the QDs-Rh101 complexes from atmospheric pressure (1atm) to 0.9 GPa, the fluorescence quenching degree of QDs gradually increases (Fig. 1(c)). Furthermore, in addition to the emission quenching of QDs in the complexes, a new emission peak is formed at 623 nm, which is attributed to FRET-mediated Rh101 fluorescence. As increasing pressure from 1atm to 0.9Gpa, the ratio of Rh101 emission intensity to QDs emission intensity gradually increase (Fig. 1(d)), indicating the high pressure facilitate energy transfer from QDs donor to Rh101 acceptor.

 figure: Fig. 1.

Fig. 1. (a) Normalized absorption (Abs) and photoluminescence (PL) spectra of QDs donor and Rh101 dye acceptor measured with 400 nm excitation. (b) Absorption spectrum of QDs-Rh101 complexes. (c) Fluorescence (Flu) spectra of QDs-Rh101 complexes under high pressure from 1atm to 0.9G. (d) The ratio of Rh101 fluorescence intensity (F623 nm) to QDs fluorescence intensity (F516 nm) upon compression.

Download Full Size | PPT Slide | PDF

Furthermore, we recorded the chromaticity coordinates of QDs-Rh101 complexes emission under high pressure from 1atm to 0.9Gpa (Fig. 2(a)) [40]. Based on CIE chromaticity diagram, the emission of QDs-Rh101 complexes at 1atm lies to the green (0.33, 0.52) and its corresponding color temperature is in the range of 5000-6000 K. As increasing pressure from 1atm to 0.9Gpa, the emission colors of the QDs-Rh101 complexes change from green to yellow. In addition, Fig. 2(b) shows fluorescent images of QDs-Rh101 complexes. The change of luminescence colors of QDs-Rh101 complexes is consistent with the CIE chromaticity diagram. The luminescence color changing is derived from the pressure-enhanced FRET from QDs donor to Rh101 acceptor. Thus, we indeed developed high pressure as a powerful tool to facilitate the FRET process, along with the change in the chromaticity of emission in the QD-molecule system. The color tunability of the QDs-molecules system permits the development of light source with different luminosity characteristics for applications, particularly military navigation marker lights, where illumination specifications need to be regulated on demand.

 figure: Fig. 2.

Fig. 2. (a) Pressure-dependent chromaticity coordinates of the emissions of QDs-Rh101 complexes. (b) The fluorescent images (dark background) of QDs-Rh101 complexes at 1atm, 0.4Gpa and 0.8Gpa.

Download Full Size | PPT Slide | PDF

To expound the FRET process and Auger recombination process, the time-resolved TA spectroscopic measurements were carried out to track the real-time dynamics of the QDs-Rh101 system [41,42]. Figure 3(a,b) show time-resolved changes of the absorption ($\mathrm{\Delta }$ A) signals for QDs alone and QDs-Rh101 complexes in aqueous solution. Above-band gap excitation at 400 nm results in “bleaching” of ground-state populations in QDs alone and QDs-Rh101 complexes, shown as negative ${\Delta }$ A signals in Fig. 3(a,b) at 533 nm. In addition, an obvious difference between QDs alone and QDs-Rh101 complexes in the spectra at same delay time occurs (Fig. 3 (c,d)). Addition of Rh101 acceptor at short femtosecond time period does not change the transient absorption response, but changes the response over long delay time $( > $ 100ps) gradually. As delay time increased from 100ps to 2 ns, a new peak occurs at 584 nm (Fig. 3(d)), which should be ascribed from the FRET-induced appearance of absorption signals at a higher energy of bleach. Furthermore, to probe the FRET with temporal resolution, the TA kinetic traces of QDs alone and QDs–Rh101 complexes with global analysis are shown in Fig. 3(e). The two temporal constant by applying double-exponential decays are obtained in QDs alone system. Combining the previous study of QDs, the shorter lifetime (0.31ps) is attributed to the carrier relaxation process, and the longer lifetime (198.27ps) is derived from Auger recombination process [36,43,44]. Similarly, the three temporal constants for QDs–Rh101 complexes were recorded with three-exponential decays. In the QDs–Rh101 complexes, a new time scale in hundreds picoseconds appears (130.26ps), which comes from the FRET from the QDs donor to the Rh101 acceptor. Figure 3(f) schematically illustrates the FRET process between QD donor and Rh101 acceptor and Auger recombination process of QDs. For highly excited QDs, Auger recombination process consumes the energy of light-excited exciton (electron-hole pair), which subsequently loses this energy in the form of heat. The FRET process results in the exciton to migrate from QDs donor to Rh101 acceptor state and induces emission of sensitized acceptor.

 figure: Fig. 3.

Fig. 3. (a) Three dimensional TA signals of the CdTe/CdS QDs alone and (b) CdTe/CdS QDs-Rh101 complexes in water solution at 1atm. (c) TA spectra of QDs alone and (d) CdTe/CdS QDs-Rh101 complexes at 1atm. (e) Kinetics of TA spectra of CdTe/CdS QDs alone and CdTe/CdS QDs-Rh101 complexes. The solid lines correspond to the fittings. (f) Schematic representation of the FRET process and Auger recombination process where energy band diagram indicates the transfer of excitons.

Download Full Size | PPT Slide | PDF

Subsequently, to explore the dependence of pressure on the FRET and Auger recombination lifetime constants, the high-pressure TA spectroscopy of QDs-Rh101 complexes was measured (Fig. S2 in Supplement 1) [45]. The TA kinetic traces of QDs–Rh101 complexes under pressure with global analysis are shown in Fig. S3. The variations in the carrier relaxation process ${\tau _1}$, FRET process ${\tau _{2}}$ and Auger recombination process ${\tau _{3}}$ as a function of pressure are shown in Fig. 4(a-c) (see Table S2 for fitting values). The ratio of Auger recombination process lifetime to FRET process lifetime under high pressure is shown in Fig. 4(d). Figure 4(a) shows that the carrier relaxation lifetime (${\tau _1}$) changes slightly under high pressure. This illustrates that high pressure has little effect on the carrier relaxation process. Importantly, for FRET process, we find that ${\tau _{2}}$ value decreases sharply and finally stabilizes as the pressure increases from 1atm to 0.9Gpa. To explain the reason, we analyzed the factors of affecting FRET rate based on Förster theory. The FRET rate strongly depends on the donor-acceptor distance and is given by Eq. (1) [15,25]:

$$k_{FRET} = \frac{1}{{\tau_D}}{\left( {\frac{{R0}}{r}} \right)^6}$$
where ${\tau _D}$ is radiative lifetime of donor and the Förster distance ${R}_0$ is the donor-acceptor distance at which the energy transfer efficiency is 50${\%}$. It can be calculated by the equation [15,25]:
$$R_0^6 = \frac{{9000\ln (10){k^2}{\varphi _D}J(\lambda )}}{{128{\pi ^5}{N_A}{s^4}}}$$
where ${\varphi _D}$ is quantum yield of the QD donor, s is the refractive index of the medium, NA is Avogadro’s number, J($\lambda $) is the spectral overlap intergral (see Supplement 1 for calculation details), k2 reflects the relative orientation of the donor and acceptor dipoles, which is a constant (k2 equals to 2/3) [15]. The donor-acceptor separation distance (r) is calculated by using [2]:
$$r = R_0{(\frac{{m(1 - E)}}{E})^{{\raise0.7ex\hbox{$1$} \!\mathord{/ {\vphantom {1 6}} }\!\lower0.7ex\hbox{$6$}}}}$$
where E is the energy transfer efficiencies (Table S1 in Supplement 1). The m is the average number of acceptor molecules attached to a donor. The m value follows a Poisson distribution, and the probability of finding a QD with n adsorbed acceptor, p(n, $\lambda )$, is given by equation [4,46]. n is the ratio of acceptor concentration to donor concentration (in our system, n equals to 5). λ is the average number of adsorbed acceptor per QDs as a function of the number of added Rh101.
$$p(n,\lambda ) = \frac{{{\lambda ^n}}}{{n!}}{e^{ - \lambda }}$$

 figure: Fig. 4.

Fig. 4. (a) Dependence of pressure on the lifetime of the carrier relaxation (${\tau _1}$), (b) FRET process (${\tau _2}$. ), and (c) Auger recombination process (${\tau _3}$). (d) Ratio of Auger recombination process lifetime to FRET process lifetime. (e) Calculated donor-acceptor distance upon compression from 1atm to 0.9Gpa. (f) The number of absorbed acceptor per QDs under pressure from 1atm to 0.9Gpa.

Download Full Size | PPT Slide | PDF

We solve Eq. (4) for $\lambda $ to yield Eq. (5).

$$\lambda ={-} \ln ({B_V}/{B_0})$$
where ${B_V}/{B_0}$ is a function of the number of added acceptor. The calculated spectral Overlap J(λ), R0, p for the QD-Rh101 system are summarized in Table 1, and the r and m are shown in Fig. 4(e,f). The m value is the p(n, $\lambda )$ obtained by the Eq. (4) multiplied by the ratio of the acceptor concentration to the donor concentration. The FRET rate [kFRET (${\tau _2}^{ - 1}$)] measured based on TA kinetic fitting. We focus on the analysis of the donor-acceptor distance and the number of absorbed molecules upon compression. As shown in Fig. 4(e,f), the r value gradually decrease. In our system, high pressure can significantly decrease water molecular volume in the liquid, which further induces a reduction in the distance between donor and acceptor. Meanwhile, the m value significantly increases as increasing pressure. This means that pressure induced the reduction of donor-acceptor distance and the increasing of the number absorbed molecules per QDs. As increasing pressure gradually, the FRET time constant is reduced from 130ps at 1atm to 6ps at 0.9 GPa.

Tables Icon

Table 1. Summary of the FRET rate (kFRET), spectral overlap J(λ), Förster distance (R0), and possibility (P) of acceptor adsorbed to QDs under several represent pressures.

For Auger recombination process, as shown in Fig. 4(c), the ${\tau _{3}}$ increases significantly as the pressure increase. We speculate that an alloying could form at the core/shell interface in CdTe/CdS QDs. With forming the interface alloy layer, the confinement potential between the core and the shell will be smoothed, which may lead to the observed Auger recombination suppression [23,47,48]. In particular, based on the calculations of Cragg and Efros, the “smooth” interface potential can decrease the Auger recombination rate by more than 3 orders of magnitude [49]. In our research, water acts as a pressure transfer medium upon compression, and a stronger squeezing effect occurs at the core/shell interface. This would lead to enhanced mutual diffusion of Te and S ions and the local strain at the core/shell interface. The local strain causes a greater mismatch between the core and shell crystal lattices, which would offer a driving force for the alloying process [50,51]. As the applied pressure increases, Auger recombination time constant increase from 200ps at 1atm to 425ps at 0.9 GPa. Finally, we observe that the FRET process can occur 70 times faster than Auger recombination process (Fig. 4(d)), indicating high pressure is an efficient tool to simultaneously facilitate the FRET and suppress Auger recombination process.

4. Conclusion

In summary, we have developed a new strategy to efficiently regulate FRET process and Auger recombination process in QDs-molecules system using in situ high-pressure tool. When applying pressure from 1atm to 0.9 GPa to the system, the FRET rate rapidly increases, however, the Auger recombination rate gradually decreases. We ascribe the high rate of FRET to the shortened donor-acceptor distance and the increased the number of adsorbed acceptor. Meanwhile, the highly suppressed Auger recombination is attributed to the formed alloying at the core/shell interface in the QDs upon compression. Intriguingly, the FRET can occur 70 times faster than Auger recombination at 0.9 GPa. The high-rate FRET process, coupled with the low-speed Auger recombination process in QDs-molecules system, suggest great progress in applications including efficient LEDs, solar cells, and optical gain media with lower threshold. Our findings not only develop a new strategy to simultaneously facilitate the FRET and suppress Auger recombination, but also arouse further fundamental research to develop potential applications of QDs-molecules systems.

Funding

National Defense Basic Scientific Research Program of China (2019YFA0307701); National Natural Science Foundation of China (11874180); Young and Middle-aged Scientific and Technological Innovation leaders and Team Projects in Jilin Province (20200301020RQ).

Disclosures

The authors declare no competing financial interests.

Data availability

Data underlying the results presented in this paper are not publicly available at this time but may be obtained from the authors upon reasonable request.

Supplemental document

See Supplement 1 for supporting content.

References

1. E. Mutlugun, O. Samarskaya, T. Ozel, N. Cicek, N. Gaponik, A. Eychmüller, and H. V. Demir, “Highly efficient nonradiative energy transfer mediated light harvesting in water using aqueous CdTe quantum dot antennas,” Opt. Express 18(10), 10720–10730 (2010). [CrossRef]  

2. A. R. Clapp, T. Pons, I. L. Medintz, J. B. Delehanty, J. S. Melinger, T. Tiefenbrunn, P. E. Dawson, B. R. Fisher, B. O’Rourke, and H. Mattoussi, “Two-photon excitation of quantum-dot-based fluorescence resonance energy transfer and its applications,” Adv. Mater. 19(15), 1921–1926 (2007). [CrossRef]  

3. S. Jana, X. Xu, A. Klymchenko, A. Reisch, and T. Pons, “Microcavity-enhanced fluorescence energy transfer from quantum dot excited whispering gallery modes to acceptor dye nanoparticles,” ACS Nano 15(1), 1445–1453 (2021). [CrossRef]  

4. W. Zhang, J. Li, H. Lei, and B. Li, “Temperature-dependent Förster resonance energy transfer from upconversion nanoparticles to quantum dots,” Opt. Express 28(8), 12450–12459 (2020). [CrossRef]  

5. G. Yang, S. Shi, X. Zhang, S. Zhou, D. Liu, Y. Liang, Z. Chen, and G. Liang, “Ultrafast photophysical process of bi-exciton Auger recombination in CuInS2 quantum dots studied by transient-absorption spectroscopy,” Opt. Express 29(6), 9012–9020 (2021). [CrossRef]  

6. P. Ghenuche, M. Mivelle, J. de Torres, S. B. Moparthi, H. Rigneault, N. F. V. Hulst, M. F. G. Parajó, and J. Wenger, “Matching nanoantenna field confinement to FRET distances enhances Förster energy transfer rates,” Nano Lett. 15(9), 6193–6201 (2015). [CrossRef]  

7. V. I. Klimov, A. A. Mikhailovsky, D. W. Mcbranch, C. A. Leatherdale, and M. G. Bawendi, “Quantization of multiparticle Auger rates in semiconductor quantum dots,” Science 287(5455), 1011–1013 (2000). [CrossRef]  

8. L. L. Ran, H. Y. Li, W. Z. Wu, Y. C. Gao, Z. J. Chai, J. Xiao, Q. H. Li, and D. G. Kong, “Ultrafast optical properties of type-ii cdzns/znse core-shell quantum dots,” Opt. Express 26(14), 18480–18491 (2018). [CrossRef]  

9. Y. L. Li and K. F. Wu, “Size and halide dependent Auger recombination in lead halide perovskite nanocrystals,” Angew. Chem. Int. Edit. 59(34), 14292–14295 (2020). [CrossRef]  

10. J. Gao, S. C. Nguyen, N. D. Bronstein, and A. P. Alivisatos, “Solution-processed, high-speed, and high-quantum-efficiency quantum dot infrared photodetectors,” ACS Photonics 3(7), 1217–1222 (2016). [CrossRef]  

11. S. Q. Ren, L. Y. Chang, S. K. Lim, J. Zhao, M. Smith, N. Zhao, V. Bulovic, M. Bawendi, and S. Gradecak, “Inorganic-organic hybrid solar cell: bridging quantum dots to conjugated polymer nanowires,” Nano Lett. 11(9), 3998–4002 (2011). [CrossRef]  

12. J. M. Pietryga, Y. S. Park, J. Lim, A. F. Fidler, W. K. Bae, S. Brovelli, and V. I. Klimov, “Spectroscopic and device aspects of nanocrystal quantum dots,” Chem. Rev. 116(18), 10513–10622 (2016). [CrossRef]  

13. V. Muhr, C. Wurth, M. Kraft, M. Buchner, A. J. Baeumner, U. Resch-Genger, and T. Hirsch, “Particle-size-dependent Förster resonance energy transfer from upconversion nanoparticles to organic dyes,” Anal. Chem. 89(9), 4868–4874 (2017). [CrossRef]  

14. B.C. Huang, L. Xu, J. L. Zhu, Y. X. Wang, B. Sun, X. P. Li, and H. B. Yang, “Real-time monitoring the dynamics of coordination-driven self-assembly by fluorescence-resonance energy transfer,” J. Am. Chem. Soc. 139(28), 9459–9462 (2017). [CrossRef]  

15. A. R. Clapp, I. L. Medintz, J. M. Mauro, B. R. Fisher, M. G. Bawendi, and H. Mattoussi, “Fluorescence resonance energy transfer between quantum dot donors and dye-labeled protein acceptors,” J. Am. Chem. Soc. 126(1), 301–310 (2004). [CrossRef]  

16. K. E. Sapsford, L. Berti, and I. L. Medintz, “Materials for fluorescence resonance energy transfer analysis: beyond traditional donor–acceptor combinations,” Angew. Chem. Int. Ed. 45(28), 4562–4589 (2006). [CrossRef]  

17. X. Hou, J. Kang, H. Qin, X. Chen, J. Ma, J. Zhou, L. Chen, L. Wang, L-W. Wang, and X. Peng, “Engineering Auger recombination in colloidal quantum dots via dielectric screening,” Nat. Commun. 10(1), 1750 (2019). [CrossRef]  

18. D. I. Chepic, Al. L. Efros, A. I. Ekimov, M. G. Ivanov, V. A. Kharchenko, I. A. Kudriavtsev, and T. V. Yazeva, “Auger ionization of semiconductor quantum drops in a glass matrix,” J. Lumin. 47(3), 113–127 (1990). [CrossRef]  

19. V. I. Klimov, “Multicarrier interactions in semiconductor nanocrystals in relation to the phenomena of Auger recombination and carrier multiplication,” Annu. Rev. Condens. Matter Phys. 5(1), 285–316 (2014). [CrossRef]  

20. R. Vaxenburg, A. Rodina, A. Shabaev, E. Lifshitz, and A. L. Efros, “Nonradiative Auger recombination in semiconductor nanocrystals,” Nano Lett. 15(3), 2092–2098 (2015). [CrossRef]  

21. A. J. P. Teunissen, C. Pérez-Medina, A. Meijerink, and W. J. M. Mulder, “Investigating supramolecular systems using Förster resonance energy transfer,” Chem. Soc. Rev. 47(18), 7027–7044 (2018). [CrossRef]  

22. L. L. Wu, C. S. Huang, B. Emery, A. C. Sedgwick, S. D. Bull, X. P. He, H. Tian, J. Yoon, J. L. Sessler, and T. D. James, “Förster resonance energy transfer (FRET)-based small-molecule sensors and imaging agents,” Chem. Soc. Rev. 49(15), 5110–5139 (2020). [CrossRef]  

23. F. Garcia-Santamaria, S. Brovelli, R. Viswanatha, J. A. Hollingsworth, H. Htoon, S. A. Crooker, and V. I. Klimov, “Breakdown of volume scaling in Auger recombination in cdse/cds heteronanocrystals: the role of the core-shell interface,” Nano Lett. 11(2), 687–693 (2011). [CrossRef]  

24. W. K. Bae, L. A. Padilha, Y. S. Park, H. McDaniel, I. Robel, J. M. Pietryga, and V. I. Klimov, “Controlled alloying of the core-shell interface in cdse/cds quantum dots for suppression of Auger recombination,” ACS Nano 7(4), 3411–3419 (2013). [CrossRef]  

25. M. Cardoso Dos Santos, W. R. Algar, I. L. Medintz, and N. Hildebrandt, “Quantum dots for Förster resonance energy transfer (FRET),” Trends Anal. Chem. 125, 115819 (2020). [CrossRef]  

26. E. Lerner, T. Cordes, A. Ingargiola, Y. Alhadid, S. Y. Chung, X. Michalet, and S. Weiss, “Toward dynamic structural biology: two decades of singer-molexule Förster resonance energy transfer,” Science359(6373), eaan1133 (2018). [CrossRef]  

27. E. Cohen, P. Komm, N. Rosenthal-Strauss, J. Dehnel, E. Lifshitz, S. Yochelis, R. D. Levine, F. Remacle, B. Fresch, G. Marcus, and Y. Paltiel, “Fast energy transfer in cdse quantum dot layered structures: controlling coupling with covalent-bond organic linkers,” J. Phys. Chem. C 122(10), 5753–5758 (2018). [CrossRef]  

28. T. Franzl, A. Shavel, A. L. Rogach, N. Gaponik, T. A. Klar, A. Eychmüller, and J. Feldmann, “High-rate unidirectional energy transfer in directly assembled cdte nanocrystal bilayers,” Small 1(4), 392–395 (2005). [CrossRef]  

29. S. Panuganti, L. V. Besteiro, E. S. Vasileiadou, J. M. Hoffman, A. O. Govorov, S. K. Gray, M. G. Kanatzidis, and R. D. Schaller, “Distance dependence of Förster resonance energy transfer rates in 2D perovskite quantum wells via control of organic spacer length,” J. Am. Chem. Soc. 143(11), 4244–4252 (2021). [CrossRef]  

30. J. Gao, H. Zhang, X. Liu, N. Zhou, X. Pi, D. Li, and D. Yang, “Plasmon-coupled Förster resonance energy transfer between silicon quantim dots,” J. Phys. Chem. C 123(38), 23604–23609 (2019). [CrossRef]  

31. L. Dworak, V. V. Matylitsky, T. Ren, T. Basche, and J. Wachtveitl, “Acceptor concentration dependence of Förster resonance energy transfer dynamics in dye-quantum dot complexes,” J. Phys. Chem. C 118(8), 4396–4402 (2014). [CrossRef]  

32. Y. S. Park, W. K. Bae, L. A. Padilha, J. M. Pietryga, and V. I. Klimov, “Effect of the core/shell interface on Auger recombination evaluated by single-quantum-dot spectroscopy,” Nano Lett. 14(2), 396–402 (2014). [CrossRef]  

33. W. Guo, J. Tang, G. Zhang, B. Li, C. Yang, R. Chen, C. Qin, J. Hu, H. Zhong, L. Xiao, and S. Jia, “Photoluminescence blinking and biexcition Auger recombination in single colloidal quantum dots with sharp and smooth core/shell interfaces,” J. Phys. Chem. Lett. 12(1), 405–412 (2021). [CrossRef]  

34. Y. S. Park, J. Lim, N. S. Makarov, and V. I. Klimov, “Effect of interfacial alloying versus “volume scaling” on Auger recombination in compositionally graded semiconductor quantum dots,” Nano Lett. 17(9), 5607–5613 (2017). [CrossRef]  

35. C. Smith and D. Binks, “Multiple exciton generation in colloidal nanocrystals,” Nanomaterials 4(1), 19–45 (2014). [CrossRef]  

36. X. Liu, J. Han, Y. Li, B. Cao, C. Sun, H. Yin, Y. Shi, M. Jin, C. Liu, M. Sun, and D. Ding, “Ultrafast carrier dynamics in all-inorganic CsPbBr3 perovskite across the pressure-induced phase transition,” Opt. Express 27(16), A995–1003 (2019). [CrossRef]  

37. W. Bi, X. Li, L. Zhang, T. Jin, L. Zhang, Q. Zhang, Y. Luo, C. Wu, and Y. Xie, “Molecular co-catalyst accelerating hole transfer for enhanced photocatalytic H2 evolution,” Nat. Commun. 6(1), 8647 (2015). [CrossRef]  

38. B. Yang, J. S. Chen, S. Q. Yang, F. Hong, L. Sun, P. G. Han, T. Pullerits, W. Q. Deng, and K. L. Han, “Lead-free silver-bismuth halide double perovskite nanocrystals,” Angew. Chem. Int. Ed. 57(19), 5359–5363 (2018). [CrossRef]  

39. C. E. Rowland, I. Fedin, H. Zhang, S. K. Gray, A. O. Govorov, D. V. Talapin, and R. D. Schaller, “Picosecond energy transfer and multiexciton transfer outpaces Auger recombination in binary cdse nanoplatelet solids,” Nature Mater 14(5), 484–489 (2015). [CrossRef]  

40. S. Pramanik, S. Bhandari, S. Roy, and A. Chattopadhyay, “Synchronous tricolor emission-based white light from quantum dot complex,” J. Phys. Chem. Lett. 6(7), 1270–1274 (2015). [CrossRef]  

41. H. Zong, J. Wang, X. Mu, X. Xu, J. Li, X. Wang, F. Long, J. Wang, and M. Sun, “Physical mechanism of photoinduced intermolecular charge transfer enhanced by fluorescence resonance energy transfer,” Phys. Chem. Chem. Phys. 20(19), 13558–13565 (2018). [CrossRef]  

42. H. Zong, X. Mu, J. Wang, H. Zhao, Y. shi, and M. Sun, “The nature of photoinduced intermolecular charge transfer in fluorescence resonance energy transfer,” Spectrochim. Acta, Part A 209(15), 228–233 (2019). [CrossRef]  

43. H. Zhu, N. Song, and T. Lian, “Controlling charge separation and recombination rates in cdse/zns type I core−shell quantum dots by shell thicknesses,” J. Am. Chem. Soc. 132(42), 15038–15045 (2010). [CrossRef]  

44. W. K. Bae, Y. S. Park, J. Lim, D. Lee, L. A. Padilha, H. McDaniel, I. Robel, C. Lee, J. M. Pietryga, and V. I. Klimov, “Controlling the influence of Auger recombination on the performance of quantum-dot light-emitting diodes,” Nat. Commun. 4(1), 2661 (2013). [CrossRef]  

45. F. Bai, K. Bian, X. Huang, Z. Wang, and H. Fan, “Pressure induced nanoparticle phase behavior, property, and applications,” Chem. Rev. 119(12), 7673–7717 (2019). [CrossRef]  

46. A. J. Morris-Cohen, M. T. Frederick, L. C. Cass, and E. A. Weiss, “Simultaneous determination of the adsorption constant and the photoinduced electron transfer rate for a cds quantum dot-violagen complex,” J. Am. Chem. Soc. 133(26), 10146–10154 (2011). [CrossRef]  

47. H.F. Zhao, H. Yin, X. C. Liu, H. Li, Y. Shi, C. L. Liu, M. X. Jin, J. B. Gao, Y. Luo, and D. J. Ding, “Pressure-induced tunable electron transfer and Auger recombination rates in cdse/zns quantum dot–anthraquinone complexes,” J. Phys. Chem. Lett. 10(11), 3064–3070 (2019). [CrossRef]  

48. J. E. Guyer and P. W. Voorhees, “Morphological stability of alloy thin films,” Phys. Rev. Lett. 74(20), 4031–4034 (1995). [CrossRef]  

49. G. E. Cragg and A. L. Efros, “Suppression of Auger processes in confined structures,” Nano Lett. 10(1), 313–317 (2010). [CrossRef]  

50. V. M. Dzhagan, M. Y. Valakh, A. E. Raevskaya, A. L. Stroyuk, S. Y. Kuchmiy, and D. R. T. Zahn, “Resonant raman scattering study of cdse nanocrystals passivated with cds and zns,” Nanotechnology 18(28), 285701 (2007). [CrossRef]  

51. S. Zou and M. J. Weaver, “Surface-enhanced raman spectroscopy of cadmium sulfide/cadmium selenide superlattices formed on gold by electrochemical atomic-layer epitaxy,” Chem. Phys. Lett. 312(2-4), 101–107 (1999). [CrossRef]  

References

  • View by:

  1. E. Mutlugun, O. Samarskaya, T. Ozel, N. Cicek, N. Gaponik, A. Eychmüller, and H. V. Demir, “Highly efficient nonradiative energy transfer mediated light harvesting in water using aqueous CdTe quantum dot antennas,” Opt. Express 18(10), 10720–10730 (2010).
    [Crossref]
  2. A. R. Clapp, T. Pons, I. L. Medintz, J. B. Delehanty, J. S. Melinger, T. Tiefenbrunn, P. E. Dawson, B. R. Fisher, B. O’Rourke, and H. Mattoussi, “Two-photon excitation of quantum-dot-based fluorescence resonance energy transfer and its applications,” Adv. Mater. 19(15), 1921–1926 (2007).
    [Crossref]
  3. S. Jana, X. Xu, A. Klymchenko, A. Reisch, and T. Pons, “Microcavity-enhanced fluorescence energy transfer from quantum dot excited whispering gallery modes to acceptor dye nanoparticles,” ACS Nano 15(1), 1445–1453 (2021).
    [Crossref]
  4. W. Zhang, J. Li, H. Lei, and B. Li, “Temperature-dependent Förster resonance energy transfer from upconversion nanoparticles to quantum dots,” Opt. Express 28(8), 12450–12459 (2020).
    [Crossref]
  5. G. Yang, S. Shi, X. Zhang, S. Zhou, D. Liu, Y. Liang, Z. Chen, and G. Liang, “Ultrafast photophysical process of bi-exciton Auger recombination in CuInS2 quantum dots studied by transient-absorption spectroscopy,” Opt. Express 29(6), 9012–9020 (2021).
    [Crossref]
  6. P. Ghenuche, M. Mivelle, J. de Torres, S. B. Moparthi, H. Rigneault, N. F. V. Hulst, M. F. G. Parajó, and J. Wenger, “Matching nanoantenna field confinement to FRET distances enhances Förster energy transfer rates,” Nano Lett. 15(9), 6193–6201 (2015).
    [Crossref]
  7. V. I. Klimov, A. A. Mikhailovsky, D. W. Mcbranch, C. A. Leatherdale, and M. G. Bawendi, “Quantization of multiparticle Auger rates in semiconductor quantum dots,” Science 287(5455), 1011–1013 (2000).
    [Crossref]
  8. L. L. Ran, H. Y. Li, W. Z. Wu, Y. C. Gao, Z. J. Chai, J. Xiao, Q. H. Li, and D. G. Kong, “Ultrafast optical properties of type-ii cdzns/znse core-shell quantum dots,” Opt. Express 26(14), 18480–18491 (2018).
    [Crossref]
  9. Y. L. Li and K. F. Wu, “Size and halide dependent Auger recombination in lead halide perovskite nanocrystals,” Angew. Chem. Int. Edit. 59(34), 14292–14295 (2020).
    [Crossref]
  10. J. Gao, S. C. Nguyen, N. D. Bronstein, and A. P. Alivisatos, “Solution-processed, high-speed, and high-quantum-efficiency quantum dot infrared photodetectors,” ACS Photonics 3(7), 1217–1222 (2016).
    [Crossref]
  11. S. Q. Ren, L. Y. Chang, S. K. Lim, J. Zhao, M. Smith, N. Zhao, V. Bulovic, M. Bawendi, and S. Gradecak, “Inorganic-organic hybrid solar cell: bridging quantum dots to conjugated polymer nanowires,” Nano Lett. 11(9), 3998–4002 (2011).
    [Crossref]
  12. J. M. Pietryga, Y. S. Park, J. Lim, A. F. Fidler, W. K. Bae, S. Brovelli, and V. I. Klimov, “Spectroscopic and device aspects of nanocrystal quantum dots,” Chem. Rev. 116(18), 10513–10622 (2016).
    [Crossref]
  13. V. Muhr, C. Wurth, M. Kraft, M. Buchner, A. J. Baeumner, U. Resch-Genger, and T. Hirsch, “Particle-size-dependent Förster resonance energy transfer from upconversion nanoparticles to organic dyes,” Anal. Chem. 89(9), 4868–4874 (2017).
    [Crossref]
  14. B.C. Huang, L. Xu, J. L. Zhu, Y. X. Wang, B. Sun, X. P. Li, and H. B. Yang, “Real-time monitoring the dynamics of coordination-driven self-assembly by fluorescence-resonance energy transfer,” J. Am. Chem. Soc. 139(28), 9459–9462 (2017).
    [Crossref]
  15. A. R. Clapp, I. L. Medintz, J. M. Mauro, B. R. Fisher, M. G. Bawendi, and H. Mattoussi, “Fluorescence resonance energy transfer between quantum dot donors and dye-labeled protein acceptors,” J. Am. Chem. Soc. 126(1), 301–310 (2004).
    [Crossref]
  16. K. E. Sapsford, L. Berti, and I. L. Medintz, “Materials for fluorescence resonance energy transfer analysis: beyond traditional donor–acceptor combinations,” Angew. Chem. Int. Ed. 45(28), 4562–4589 (2006).
    [Crossref]
  17. X. Hou, J. Kang, H. Qin, X. Chen, J. Ma, J. Zhou, L. Chen, L. Wang, L-W. Wang, and X. Peng, “Engineering Auger recombination in colloidal quantum dots via dielectric screening,” Nat. Commun. 10(1), 1750 (2019).
    [Crossref]
  18. D. I. Chepic, Al. L. Efros, A. I. Ekimov, M. G. Ivanov, V. A. Kharchenko, I. A. Kudriavtsev, and T. V. Yazeva, “Auger ionization of semiconductor quantum drops in a glass matrix,” J. Lumin. 47(3), 113–127 (1990).
    [Crossref]
  19. V. I. Klimov, “Multicarrier interactions in semiconductor nanocrystals in relation to the phenomena of Auger recombination and carrier multiplication,” Annu. Rev. Condens. Matter Phys. 5(1), 285–316 (2014).
    [Crossref]
  20. R. Vaxenburg, A. Rodina, A. Shabaev, E. Lifshitz, and A. L. Efros, “Nonradiative Auger recombination in semiconductor nanocrystals,” Nano Lett. 15(3), 2092–2098 (2015).
    [Crossref]
  21. A. J. P. Teunissen, C. Pérez-Medina, A. Meijerink, and W. J. M. Mulder, “Investigating supramolecular systems using Förster resonance energy transfer,” Chem. Soc. Rev. 47(18), 7027–7044 (2018).
    [Crossref]
  22. L. L. Wu, C. S. Huang, B. Emery, A. C. Sedgwick, S. D. Bull, X. P. He, H. Tian, J. Yoon, J. L. Sessler, and T. D. James, “Förster resonance energy transfer (FRET)-based small-molecule sensors and imaging agents,” Chem. Soc. Rev. 49(15), 5110–5139 (2020).
    [Crossref]
  23. F. Garcia-Santamaria, S. Brovelli, R. Viswanatha, J. A. Hollingsworth, H. Htoon, S. A. Crooker, and V. I. Klimov, “Breakdown of volume scaling in Auger recombination in cdse/cds heteronanocrystals: the role of the core-shell interface,” Nano Lett. 11(2), 687–693 (2011).
    [Crossref]
  24. W. K. Bae, L. A. Padilha, Y. S. Park, H. McDaniel, I. Robel, J. M. Pietryga, and V. I. Klimov, “Controlled alloying of the core-shell interface in cdse/cds quantum dots for suppression of Auger recombination,” ACS Nano 7(4), 3411–3419 (2013).
    [Crossref]
  25. M. Cardoso Dos Santos, W. R. Algar, I. L. Medintz, and N. Hildebrandt, “Quantum dots for Förster resonance energy transfer (FRET),” Trends Anal. Chem. 125, 115819 (2020).
    [Crossref]
  26. E. Lerner, T. Cordes, A. Ingargiola, Y. Alhadid, S. Y. Chung, X. Michalet, and S. Weiss, “Toward dynamic structural biology: two decades of singer-molexule Förster resonance energy transfer,” Science359(6373), eaan1133 (2018).
    [Crossref]
  27. E. Cohen, P. Komm, N. Rosenthal-Strauss, J. Dehnel, E. Lifshitz, S. Yochelis, R. D. Levine, F. Remacle, B. Fresch, G. Marcus, and Y. Paltiel, “Fast energy transfer in cdse quantum dot layered structures: controlling coupling with covalent-bond organic linkers,” J. Phys. Chem. C 122(10), 5753–5758 (2018).
    [Crossref]
  28. T. Franzl, A. Shavel, A. L. Rogach, N. Gaponik, T. A. Klar, A. Eychmüller, and J. Feldmann, “High-rate unidirectional energy transfer in directly assembled cdte nanocrystal bilayers,” Small 1(4), 392–395 (2005).
    [Crossref]
  29. S. Panuganti, L. V. Besteiro, E. S. Vasileiadou, J. M. Hoffman, A. O. Govorov, S. K. Gray, M. G. Kanatzidis, and R. D. Schaller, “Distance dependence of Förster resonance energy transfer rates in 2D perovskite quantum wells via control of organic spacer length,” J. Am. Chem. Soc. 143(11), 4244–4252 (2021).
    [Crossref]
  30. J. Gao, H. Zhang, X. Liu, N. Zhou, X. Pi, D. Li, and D. Yang, “Plasmon-coupled Förster resonance energy transfer between silicon quantim dots,” J. Phys. Chem. C 123(38), 23604–23609 (2019).
    [Crossref]
  31. L. Dworak, V. V. Matylitsky, T. Ren, T. Basche, and J. Wachtveitl, “Acceptor concentration dependence of Förster resonance energy transfer dynamics in dye-quantum dot complexes,” J. Phys. Chem. C 118(8), 4396–4402 (2014).
    [Crossref]
  32. Y. S. Park, W. K. Bae, L. A. Padilha, J. M. Pietryga, and V. I. Klimov, “Effect of the core/shell interface on Auger recombination evaluated by single-quantum-dot spectroscopy,” Nano Lett. 14(2), 396–402 (2014).
    [Crossref]
  33. W. Guo, J. Tang, G. Zhang, B. Li, C. Yang, R. Chen, C. Qin, J. Hu, H. Zhong, L. Xiao, and S. Jia, “Photoluminescence blinking and biexcition Auger recombination in single colloidal quantum dots with sharp and smooth core/shell interfaces,” J. Phys. Chem. Lett. 12(1), 405–412 (2021).
    [Crossref]
  34. Y. S. Park, J. Lim, N. S. Makarov, and V. I. Klimov, “Effect of interfacial alloying versus “volume scaling” on Auger recombination in compositionally graded semiconductor quantum dots,” Nano Lett. 17(9), 5607–5613 (2017).
    [Crossref]
  35. C. Smith and D. Binks, “Multiple exciton generation in colloidal nanocrystals,” Nanomaterials 4(1), 19–45 (2014).
    [Crossref]
  36. X. Liu, J. Han, Y. Li, B. Cao, C. Sun, H. Yin, Y. Shi, M. Jin, C. Liu, M. Sun, and D. Ding, “Ultrafast carrier dynamics in all-inorganic CsPbBr3 perovskite across the pressure-induced phase transition,” Opt. Express 27(16), A995–1003 (2019).
    [Crossref]
  37. W. Bi, X. Li, L. Zhang, T. Jin, L. Zhang, Q. Zhang, Y. Luo, C. Wu, and Y. Xie, “Molecular co-catalyst accelerating hole transfer for enhanced photocatalytic H2 evolution,” Nat. Commun. 6(1), 8647 (2015).
    [Crossref]
  38. B. Yang, J. S. Chen, S. Q. Yang, F. Hong, L. Sun, P. G. Han, T. Pullerits, W. Q. Deng, and K. L. Han, “Lead-free silver-bismuth halide double perovskite nanocrystals,” Angew. Chem. Int. Ed. 57(19), 5359–5363 (2018).
    [Crossref]
  39. C. E. Rowland, I. Fedin, H. Zhang, S. K. Gray, A. O. Govorov, D. V. Talapin, and R. D. Schaller, “Picosecond energy transfer and multiexciton transfer outpaces Auger recombination in binary cdse nanoplatelet solids,” Nature Mater 14(5), 484–489 (2015).
    [Crossref]
  40. S. Pramanik, S. Bhandari, S. Roy, and A. Chattopadhyay, “Synchronous tricolor emission-based white light from quantum dot complex,” J. Phys. Chem. Lett. 6(7), 1270–1274 (2015).
    [Crossref]
  41. H. Zong, J. Wang, X. Mu, X. Xu, J. Li, X. Wang, F. Long, J. Wang, and M. Sun, “Physical mechanism of photoinduced intermolecular charge transfer enhanced by fluorescence resonance energy transfer,” Phys. Chem. Chem. Phys. 20(19), 13558–13565 (2018).
    [Crossref]
  42. H. Zong, X. Mu, J. Wang, H. Zhao, Y. shi, and M. Sun, “The nature of photoinduced intermolecular charge transfer in fluorescence resonance energy transfer,” Spectrochim. Acta, Part A 209(15), 228–233 (2019).
    [Crossref]
  43. H. Zhu, N. Song, and T. Lian, “Controlling charge separation and recombination rates in cdse/zns type I core−shell quantum dots by shell thicknesses,” J. Am. Chem. Soc. 132(42), 15038–15045 (2010).
    [Crossref]
  44. W. K. Bae, Y. S. Park, J. Lim, D. Lee, L. A. Padilha, H. McDaniel, I. Robel, C. Lee, J. M. Pietryga, and V. I. Klimov, “Controlling the influence of Auger recombination on the performance of quantum-dot light-emitting diodes,” Nat. Commun. 4(1), 2661 (2013).
    [Crossref]
  45. F. Bai, K. Bian, X. Huang, Z. Wang, and H. Fan, “Pressure induced nanoparticle phase behavior, property, and applications,” Chem. Rev. 119(12), 7673–7717 (2019).
    [Crossref]
  46. A. J. Morris-Cohen, M. T. Frederick, L. C. Cass, and E. A. Weiss, “Simultaneous determination of the adsorption constant and the photoinduced electron transfer rate for a cds quantum dot-violagen complex,” J. Am. Chem. Soc. 133(26), 10146–10154 (2011).
    [Crossref]
  47. H.F. Zhao, H. Yin, X. C. Liu, H. Li, Y. Shi, C. L. Liu, M. X. Jin, J. B. Gao, Y. Luo, and D. J. Ding, “Pressure-induced tunable electron transfer and Auger recombination rates in cdse/zns quantum dot–anthraquinone complexes,” J. Phys. Chem. Lett. 10(11), 3064–3070 (2019).
    [Crossref]
  48. J. E. Guyer and P. W. Voorhees, “Morphological stability of alloy thin films,” Phys. Rev. Lett. 74(20), 4031–4034 (1995).
    [Crossref]
  49. G. E. Cragg and A. L. Efros, “Suppression of Auger processes in confined structures,” Nano Lett. 10(1), 313–317 (2010).
    [Crossref]
  50. V. M. Dzhagan, M. Y. Valakh, A. E. Raevskaya, A. L. Stroyuk, S. Y. Kuchmiy, and D. R. T. Zahn, “Resonant raman scattering study of cdse nanocrystals passivated with cds and zns,” Nanotechnology 18(28), 285701 (2007).
    [Crossref]
  51. S. Zou and M. J. Weaver, “Surface-enhanced raman spectroscopy of cadmium sulfide/cadmium selenide superlattices formed on gold by electrochemical atomic-layer epitaxy,” Chem. Phys. Lett. 312(2-4), 101–107 (1999).
    [Crossref]

2021 (4)

S. Jana, X. Xu, A. Klymchenko, A. Reisch, and T. Pons, “Microcavity-enhanced fluorescence energy transfer from quantum dot excited whispering gallery modes to acceptor dye nanoparticles,” ACS Nano 15(1), 1445–1453 (2021).
[Crossref]

G. Yang, S. Shi, X. Zhang, S. Zhou, D. Liu, Y. Liang, Z. Chen, and G. Liang, “Ultrafast photophysical process of bi-exciton Auger recombination in CuInS2 quantum dots studied by transient-absorption spectroscopy,” Opt. Express 29(6), 9012–9020 (2021).
[Crossref]

S. Panuganti, L. V. Besteiro, E. S. Vasileiadou, J. M. Hoffman, A. O. Govorov, S. K. Gray, M. G. Kanatzidis, and R. D. Schaller, “Distance dependence of Förster resonance energy transfer rates in 2D perovskite quantum wells via control of organic spacer length,” J. Am. Chem. Soc. 143(11), 4244–4252 (2021).
[Crossref]

W. Guo, J. Tang, G. Zhang, B. Li, C. Yang, R. Chen, C. Qin, J. Hu, H. Zhong, L. Xiao, and S. Jia, “Photoluminescence blinking and biexcition Auger recombination in single colloidal quantum dots with sharp and smooth core/shell interfaces,” J. Phys. Chem. Lett. 12(1), 405–412 (2021).
[Crossref]

2020 (4)

M. Cardoso Dos Santos, W. R. Algar, I. L. Medintz, and N. Hildebrandt, “Quantum dots for Förster resonance energy transfer (FRET),” Trends Anal. Chem. 125, 115819 (2020).
[Crossref]

L. L. Wu, C. S. Huang, B. Emery, A. C. Sedgwick, S. D. Bull, X. P. He, H. Tian, J. Yoon, J. L. Sessler, and T. D. James, “Förster resonance energy transfer (FRET)-based small-molecule sensors and imaging agents,” Chem. Soc. Rev. 49(15), 5110–5139 (2020).
[Crossref]

Y. L. Li and K. F. Wu, “Size and halide dependent Auger recombination in lead halide perovskite nanocrystals,” Angew. Chem. Int. Edit. 59(34), 14292–14295 (2020).
[Crossref]

W. Zhang, J. Li, H. Lei, and B. Li, “Temperature-dependent Förster resonance energy transfer from upconversion nanoparticles to quantum dots,” Opt. Express 28(8), 12450–12459 (2020).
[Crossref]

2019 (6)

X. Hou, J. Kang, H. Qin, X. Chen, J. Ma, J. Zhou, L. Chen, L. Wang, L-W. Wang, and X. Peng, “Engineering Auger recombination in colloidal quantum dots via dielectric screening,” Nat. Commun. 10(1), 1750 (2019).
[Crossref]

J. Gao, H. Zhang, X. Liu, N. Zhou, X. Pi, D. Li, and D. Yang, “Plasmon-coupled Förster resonance energy transfer between silicon quantim dots,” J. Phys. Chem. C 123(38), 23604–23609 (2019).
[Crossref]

X. Liu, J. Han, Y. Li, B. Cao, C. Sun, H. Yin, Y. Shi, M. Jin, C. Liu, M. Sun, and D. Ding, “Ultrafast carrier dynamics in all-inorganic CsPbBr3 perovskite across the pressure-induced phase transition,” Opt. Express 27(16), A995–1003 (2019).
[Crossref]

H. Zong, X. Mu, J. Wang, H. Zhao, Y. shi, and M. Sun, “The nature of photoinduced intermolecular charge transfer in fluorescence resonance energy transfer,” Spectrochim. Acta, Part A 209(15), 228–233 (2019).
[Crossref]

F. Bai, K. Bian, X. Huang, Z. Wang, and H. Fan, “Pressure induced nanoparticle phase behavior, property, and applications,” Chem. Rev. 119(12), 7673–7717 (2019).
[Crossref]

H.F. Zhao, H. Yin, X. C. Liu, H. Li, Y. Shi, C. L. Liu, M. X. Jin, J. B. Gao, Y. Luo, and D. J. Ding, “Pressure-induced tunable electron transfer and Auger recombination rates in cdse/zns quantum dot–anthraquinone complexes,” J. Phys. Chem. Lett. 10(11), 3064–3070 (2019).
[Crossref]

2018 (5)

H. Zong, J. Wang, X. Mu, X. Xu, J. Li, X. Wang, F. Long, J. Wang, and M. Sun, “Physical mechanism of photoinduced intermolecular charge transfer enhanced by fluorescence resonance energy transfer,” Phys. Chem. Chem. Phys. 20(19), 13558–13565 (2018).
[Crossref]

B. Yang, J. S. Chen, S. Q. Yang, F. Hong, L. Sun, P. G. Han, T. Pullerits, W. Q. Deng, and K. L. Han, “Lead-free silver-bismuth halide double perovskite nanocrystals,” Angew. Chem. Int. Ed. 57(19), 5359–5363 (2018).
[Crossref]

E. Cohen, P. Komm, N. Rosenthal-Strauss, J. Dehnel, E. Lifshitz, S. Yochelis, R. D. Levine, F. Remacle, B. Fresch, G. Marcus, and Y. Paltiel, “Fast energy transfer in cdse quantum dot layered structures: controlling coupling with covalent-bond organic linkers,” J. Phys. Chem. C 122(10), 5753–5758 (2018).
[Crossref]

A. J. P. Teunissen, C. Pérez-Medina, A. Meijerink, and W. J. M. Mulder, “Investigating supramolecular systems using Förster resonance energy transfer,” Chem. Soc. Rev. 47(18), 7027–7044 (2018).
[Crossref]

L. L. Ran, H. Y. Li, W. Z. Wu, Y. C. Gao, Z. J. Chai, J. Xiao, Q. H. Li, and D. G. Kong, “Ultrafast optical properties of type-ii cdzns/znse core-shell quantum dots,” Opt. Express 26(14), 18480–18491 (2018).
[Crossref]

2017 (3)

V. Muhr, C. Wurth, M. Kraft, M. Buchner, A. J. Baeumner, U. Resch-Genger, and T. Hirsch, “Particle-size-dependent Förster resonance energy transfer from upconversion nanoparticles to organic dyes,” Anal. Chem. 89(9), 4868–4874 (2017).
[Crossref]

B.C. Huang, L. Xu, J. L. Zhu, Y. X. Wang, B. Sun, X. P. Li, and H. B. Yang, “Real-time monitoring the dynamics of coordination-driven self-assembly by fluorescence-resonance energy transfer,” J. Am. Chem. Soc. 139(28), 9459–9462 (2017).
[Crossref]

Y. S. Park, J. Lim, N. S. Makarov, and V. I. Klimov, “Effect of interfacial alloying versus “volume scaling” on Auger recombination in compositionally graded semiconductor quantum dots,” Nano Lett. 17(9), 5607–5613 (2017).
[Crossref]

2016 (2)

J. M. Pietryga, Y. S. Park, J. Lim, A. F. Fidler, W. K. Bae, S. Brovelli, and V. I. Klimov, “Spectroscopic and device aspects of nanocrystal quantum dots,” Chem. Rev. 116(18), 10513–10622 (2016).
[Crossref]

J. Gao, S. C. Nguyen, N. D. Bronstein, and A. P. Alivisatos, “Solution-processed, high-speed, and high-quantum-efficiency quantum dot infrared photodetectors,” ACS Photonics 3(7), 1217–1222 (2016).
[Crossref]

2015 (5)

P. Ghenuche, M. Mivelle, J. de Torres, S. B. Moparthi, H. Rigneault, N. F. V. Hulst, M. F. G. Parajó, and J. Wenger, “Matching nanoantenna field confinement to FRET distances enhances Förster energy transfer rates,” Nano Lett. 15(9), 6193–6201 (2015).
[Crossref]

C. E. Rowland, I. Fedin, H. Zhang, S. K. Gray, A. O. Govorov, D. V. Talapin, and R. D. Schaller, “Picosecond energy transfer and multiexciton transfer outpaces Auger recombination in binary cdse nanoplatelet solids,” Nature Mater 14(5), 484–489 (2015).
[Crossref]

S. Pramanik, S. Bhandari, S. Roy, and A. Chattopadhyay, “Synchronous tricolor emission-based white light from quantum dot complex,” J. Phys. Chem. Lett. 6(7), 1270–1274 (2015).
[Crossref]

W. Bi, X. Li, L. Zhang, T. Jin, L. Zhang, Q. Zhang, Y. Luo, C. Wu, and Y. Xie, “Molecular co-catalyst accelerating hole transfer for enhanced photocatalytic H2 evolution,” Nat. Commun. 6(1), 8647 (2015).
[Crossref]

R. Vaxenburg, A. Rodina, A. Shabaev, E. Lifshitz, and A. L. Efros, “Nonradiative Auger recombination in semiconductor nanocrystals,” Nano Lett. 15(3), 2092–2098 (2015).
[Crossref]

2014 (4)

L. Dworak, V. V. Matylitsky, T. Ren, T. Basche, and J. Wachtveitl, “Acceptor concentration dependence of Förster resonance energy transfer dynamics in dye-quantum dot complexes,” J. Phys. Chem. C 118(8), 4396–4402 (2014).
[Crossref]

Y. S. Park, W. K. Bae, L. A. Padilha, J. M. Pietryga, and V. I. Klimov, “Effect of the core/shell interface on Auger recombination evaluated by single-quantum-dot spectroscopy,” Nano Lett. 14(2), 396–402 (2014).
[Crossref]

C. Smith and D. Binks, “Multiple exciton generation in colloidal nanocrystals,” Nanomaterials 4(1), 19–45 (2014).
[Crossref]

V. I. Klimov, “Multicarrier interactions in semiconductor nanocrystals in relation to the phenomena of Auger recombination and carrier multiplication,” Annu. Rev. Condens. Matter Phys. 5(1), 285–316 (2014).
[Crossref]

2013 (2)

W. K. Bae, L. A. Padilha, Y. S. Park, H. McDaniel, I. Robel, J. M. Pietryga, and V. I. Klimov, “Controlled alloying of the core-shell interface in cdse/cds quantum dots for suppression of Auger recombination,” ACS Nano 7(4), 3411–3419 (2013).
[Crossref]

W. K. Bae, Y. S. Park, J. Lim, D. Lee, L. A. Padilha, H. McDaniel, I. Robel, C. Lee, J. M. Pietryga, and V. I. Klimov, “Controlling the influence of Auger recombination on the performance of quantum-dot light-emitting diodes,” Nat. Commun. 4(1), 2661 (2013).
[Crossref]

2011 (3)

A. J. Morris-Cohen, M. T. Frederick, L. C. Cass, and E. A. Weiss, “Simultaneous determination of the adsorption constant and the photoinduced electron transfer rate for a cds quantum dot-violagen complex,” J. Am. Chem. Soc. 133(26), 10146–10154 (2011).
[Crossref]

S. Q. Ren, L. Y. Chang, S. K. Lim, J. Zhao, M. Smith, N. Zhao, V. Bulovic, M. Bawendi, and S. Gradecak, “Inorganic-organic hybrid solar cell: bridging quantum dots to conjugated polymer nanowires,” Nano Lett. 11(9), 3998–4002 (2011).
[Crossref]

F. Garcia-Santamaria, S. Brovelli, R. Viswanatha, J. A. Hollingsworth, H. Htoon, S. A. Crooker, and V. I. Klimov, “Breakdown of volume scaling in Auger recombination in cdse/cds heteronanocrystals: the role of the core-shell interface,” Nano Lett. 11(2), 687–693 (2011).
[Crossref]

2010 (3)

E. Mutlugun, O. Samarskaya, T. Ozel, N. Cicek, N. Gaponik, A. Eychmüller, and H. V. Demir, “Highly efficient nonradiative energy transfer mediated light harvesting in water using aqueous CdTe quantum dot antennas,” Opt. Express 18(10), 10720–10730 (2010).
[Crossref]

H. Zhu, N. Song, and T. Lian, “Controlling charge separation and recombination rates in cdse/zns type I core−shell quantum dots by shell thicknesses,” J. Am. Chem. Soc. 132(42), 15038–15045 (2010).
[Crossref]

G. E. Cragg and A. L. Efros, “Suppression of Auger processes in confined structures,” Nano Lett. 10(1), 313–317 (2010).
[Crossref]

2007 (2)

V. M. Dzhagan, M. Y. Valakh, A. E. Raevskaya, A. L. Stroyuk, S. Y. Kuchmiy, and D. R. T. Zahn, “Resonant raman scattering study of cdse nanocrystals passivated with cds and zns,” Nanotechnology 18(28), 285701 (2007).
[Crossref]

A. R. Clapp, T. Pons, I. L. Medintz, J. B. Delehanty, J. S. Melinger, T. Tiefenbrunn, P. E. Dawson, B. R. Fisher, B. O’Rourke, and H. Mattoussi, “Two-photon excitation of quantum-dot-based fluorescence resonance energy transfer and its applications,” Adv. Mater. 19(15), 1921–1926 (2007).
[Crossref]

2006 (1)

K. E. Sapsford, L. Berti, and I. L. Medintz, “Materials for fluorescence resonance energy transfer analysis: beyond traditional donor–acceptor combinations,” Angew. Chem. Int. Ed. 45(28), 4562–4589 (2006).
[Crossref]

2005 (1)

T. Franzl, A. Shavel, A. L. Rogach, N. Gaponik, T. A. Klar, A. Eychmüller, and J. Feldmann, “High-rate unidirectional energy transfer in directly assembled cdte nanocrystal bilayers,” Small 1(4), 392–395 (2005).
[Crossref]

2004 (1)

A. R. Clapp, I. L. Medintz, J. M. Mauro, B. R. Fisher, M. G. Bawendi, and H. Mattoussi, “Fluorescence resonance energy transfer between quantum dot donors and dye-labeled protein acceptors,” J. Am. Chem. Soc. 126(1), 301–310 (2004).
[Crossref]

2000 (1)

V. I. Klimov, A. A. Mikhailovsky, D. W. Mcbranch, C. A. Leatherdale, and M. G. Bawendi, “Quantization of multiparticle Auger rates in semiconductor quantum dots,” Science 287(5455), 1011–1013 (2000).
[Crossref]

1999 (1)

S. Zou and M. J. Weaver, “Surface-enhanced raman spectroscopy of cadmium sulfide/cadmium selenide superlattices formed on gold by electrochemical atomic-layer epitaxy,” Chem. Phys. Lett. 312(2-4), 101–107 (1999).
[Crossref]

1995 (1)

J. E. Guyer and P. W. Voorhees, “Morphological stability of alloy thin films,” Phys. Rev. Lett. 74(20), 4031–4034 (1995).
[Crossref]

1990 (1)

D. I. Chepic, Al. L. Efros, A. I. Ekimov, M. G. Ivanov, V. A. Kharchenko, I. A. Kudriavtsev, and T. V. Yazeva, “Auger ionization of semiconductor quantum drops in a glass matrix,” J. Lumin. 47(3), 113–127 (1990).
[Crossref]

Algar, W. R.

M. Cardoso Dos Santos, W. R. Algar, I. L. Medintz, and N. Hildebrandt, “Quantum dots for Förster resonance energy transfer (FRET),” Trends Anal. Chem. 125, 115819 (2020).
[Crossref]

Alhadid, Y.

E. Lerner, T. Cordes, A. Ingargiola, Y. Alhadid, S. Y. Chung, X. Michalet, and S. Weiss, “Toward dynamic structural biology: two decades of singer-molexule Förster resonance energy transfer,” Science359(6373), eaan1133 (2018).
[Crossref]

Alivisatos, A. P.

J. Gao, S. C. Nguyen, N. D. Bronstein, and A. P. Alivisatos, “Solution-processed, high-speed, and high-quantum-efficiency quantum dot infrared photodetectors,” ACS Photonics 3(7), 1217–1222 (2016).
[Crossref]

Bae, W. K.

J. M. Pietryga, Y. S. Park, J. Lim, A. F. Fidler, W. K. Bae, S. Brovelli, and V. I. Klimov, “Spectroscopic and device aspects of nanocrystal quantum dots,” Chem. Rev. 116(18), 10513–10622 (2016).
[Crossref]

Y. S. Park, W. K. Bae, L. A. Padilha, J. M. Pietryga, and V. I. Klimov, “Effect of the core/shell interface on Auger recombination evaluated by single-quantum-dot spectroscopy,” Nano Lett. 14(2), 396–402 (2014).
[Crossref]

W. K. Bae, Y. S. Park, J. Lim, D. Lee, L. A. Padilha, H. McDaniel, I. Robel, C. Lee, J. M. Pietryga, and V. I. Klimov, “Controlling the influence of Auger recombination on the performance of quantum-dot light-emitting diodes,” Nat. Commun. 4(1), 2661 (2013).
[Crossref]

W. K. Bae, L. A. Padilha, Y. S. Park, H. McDaniel, I. Robel, J. M. Pietryga, and V. I. Klimov, “Controlled alloying of the core-shell interface in cdse/cds quantum dots for suppression of Auger recombination,” ACS Nano 7(4), 3411–3419 (2013).
[Crossref]

Baeumner, A. J.

V. Muhr, C. Wurth, M. Kraft, M. Buchner, A. J. Baeumner, U. Resch-Genger, and T. Hirsch, “Particle-size-dependent Förster resonance energy transfer from upconversion nanoparticles to organic dyes,” Anal. Chem. 89(9), 4868–4874 (2017).
[Crossref]

Bai, F.

F. Bai, K. Bian, X. Huang, Z. Wang, and H. Fan, “Pressure induced nanoparticle phase behavior, property, and applications,” Chem. Rev. 119(12), 7673–7717 (2019).
[Crossref]

Basche, T.

L. Dworak, V. V. Matylitsky, T. Ren, T. Basche, and J. Wachtveitl, “Acceptor concentration dependence of Förster resonance energy transfer dynamics in dye-quantum dot complexes,” J. Phys. Chem. C 118(8), 4396–4402 (2014).
[Crossref]

Bawendi, M.

S. Q. Ren, L. Y. Chang, S. K. Lim, J. Zhao, M. Smith, N. Zhao, V. Bulovic, M. Bawendi, and S. Gradecak, “Inorganic-organic hybrid solar cell: bridging quantum dots to conjugated polymer nanowires,” Nano Lett. 11(9), 3998–4002 (2011).
[Crossref]

Bawendi, M. G.

A. R. Clapp, I. L. Medintz, J. M. Mauro, B. R. Fisher, M. G. Bawendi, and H. Mattoussi, “Fluorescence resonance energy transfer between quantum dot donors and dye-labeled protein acceptors,” J. Am. Chem. Soc. 126(1), 301–310 (2004).
[Crossref]

V. I. Klimov, A. A. Mikhailovsky, D. W. Mcbranch, C. A. Leatherdale, and M. G. Bawendi, “Quantization of multiparticle Auger rates in semiconductor quantum dots,” Science 287(5455), 1011–1013 (2000).
[Crossref]

Berti, L.

K. E. Sapsford, L. Berti, and I. L. Medintz, “Materials for fluorescence resonance energy transfer analysis: beyond traditional donor–acceptor combinations,” Angew. Chem. Int. Ed. 45(28), 4562–4589 (2006).
[Crossref]

Besteiro, L. V.

S. Panuganti, L. V. Besteiro, E. S. Vasileiadou, J. M. Hoffman, A. O. Govorov, S. K. Gray, M. G. Kanatzidis, and R. D. Schaller, “Distance dependence of Förster resonance energy transfer rates in 2D perovskite quantum wells via control of organic spacer length,” J. Am. Chem. Soc. 143(11), 4244–4252 (2021).
[Crossref]

Bhandari, S.

S. Pramanik, S. Bhandari, S. Roy, and A. Chattopadhyay, “Synchronous tricolor emission-based white light from quantum dot complex,” J. Phys. Chem. Lett. 6(7), 1270–1274 (2015).
[Crossref]

Bi, W.

W. Bi, X. Li, L. Zhang, T. Jin, L. Zhang, Q. Zhang, Y. Luo, C. Wu, and Y. Xie, “Molecular co-catalyst accelerating hole transfer for enhanced photocatalytic H2 evolution,” Nat. Commun. 6(1), 8647 (2015).
[Crossref]

Bian, K.

F. Bai, K. Bian, X. Huang, Z. Wang, and H. Fan, “Pressure induced nanoparticle phase behavior, property, and applications,” Chem. Rev. 119(12), 7673–7717 (2019).
[Crossref]

Binks, D.

C. Smith and D. Binks, “Multiple exciton generation in colloidal nanocrystals,” Nanomaterials 4(1), 19–45 (2014).
[Crossref]

Bronstein, N. D.

J. Gao, S. C. Nguyen, N. D. Bronstein, and A. P. Alivisatos, “Solution-processed, high-speed, and high-quantum-efficiency quantum dot infrared photodetectors,” ACS Photonics 3(7), 1217–1222 (2016).
[Crossref]

Brovelli, S.

J. M. Pietryga, Y. S. Park, J. Lim, A. F. Fidler, W. K. Bae, S. Brovelli, and V. I. Klimov, “Spectroscopic and device aspects of nanocrystal quantum dots,” Chem. Rev. 116(18), 10513–10622 (2016).
[Crossref]

F. Garcia-Santamaria, S. Brovelli, R. Viswanatha, J. A. Hollingsworth, H. Htoon, S. A. Crooker, and V. I. Klimov, “Breakdown of volume scaling in Auger recombination in cdse/cds heteronanocrystals: the role of the core-shell interface,” Nano Lett. 11(2), 687–693 (2011).
[Crossref]

Buchner, M.

V. Muhr, C. Wurth, M. Kraft, M. Buchner, A. J. Baeumner, U. Resch-Genger, and T. Hirsch, “Particle-size-dependent Förster resonance energy transfer from upconversion nanoparticles to organic dyes,” Anal. Chem. 89(9), 4868–4874 (2017).
[Crossref]

Bull, S. D.

L. L. Wu, C. S. Huang, B. Emery, A. C. Sedgwick, S. D. Bull, X. P. He, H. Tian, J. Yoon, J. L. Sessler, and T. D. James, “Förster resonance energy transfer (FRET)-based small-molecule sensors and imaging agents,” Chem. Soc. Rev. 49(15), 5110–5139 (2020).
[Crossref]

Bulovic, V.

S. Q. Ren, L. Y. Chang, S. K. Lim, J. Zhao, M. Smith, N. Zhao, V. Bulovic, M. Bawendi, and S. Gradecak, “Inorganic-organic hybrid solar cell: bridging quantum dots to conjugated polymer nanowires,” Nano Lett. 11(9), 3998–4002 (2011).
[Crossref]

Cao, B.

Cardoso Dos Santos, M.

M. Cardoso Dos Santos, W. R. Algar, I. L. Medintz, and N. Hildebrandt, “Quantum dots for Förster resonance energy transfer (FRET),” Trends Anal. Chem. 125, 115819 (2020).
[Crossref]

Cass, L. C.

A. J. Morris-Cohen, M. T. Frederick, L. C. Cass, and E. A. Weiss, “Simultaneous determination of the adsorption constant and the photoinduced electron transfer rate for a cds quantum dot-violagen complex,” J. Am. Chem. Soc. 133(26), 10146–10154 (2011).
[Crossref]

Chai, Z. J.

Chang, L. Y.

S. Q. Ren, L. Y. Chang, S. K. Lim, J. Zhao, M. Smith, N. Zhao, V. Bulovic, M. Bawendi, and S. Gradecak, “Inorganic-organic hybrid solar cell: bridging quantum dots to conjugated polymer nanowires,” Nano Lett. 11(9), 3998–4002 (2011).
[Crossref]

Chattopadhyay, A.

S. Pramanik, S. Bhandari, S. Roy, and A. Chattopadhyay, “Synchronous tricolor emission-based white light from quantum dot complex,” J. Phys. Chem. Lett. 6(7), 1270–1274 (2015).
[Crossref]

Chen, J. S.

B. Yang, J. S. Chen, S. Q. Yang, F. Hong, L. Sun, P. G. Han, T. Pullerits, W. Q. Deng, and K. L. Han, “Lead-free silver-bismuth halide double perovskite nanocrystals,” Angew. Chem. Int. Ed. 57(19), 5359–5363 (2018).
[Crossref]

Chen, L.

X. Hou, J. Kang, H. Qin, X. Chen, J. Ma, J. Zhou, L. Chen, L. Wang, L-W. Wang, and X. Peng, “Engineering Auger recombination in colloidal quantum dots via dielectric screening,” Nat. Commun. 10(1), 1750 (2019).
[Crossref]

Chen, R.

W. Guo, J. Tang, G. Zhang, B. Li, C. Yang, R. Chen, C. Qin, J. Hu, H. Zhong, L. Xiao, and S. Jia, “Photoluminescence blinking and biexcition Auger recombination in single colloidal quantum dots with sharp and smooth core/shell interfaces,” J. Phys. Chem. Lett. 12(1), 405–412 (2021).
[Crossref]

Chen, X.

X. Hou, J. Kang, H. Qin, X. Chen, J. Ma, J. Zhou, L. Chen, L. Wang, L-W. Wang, and X. Peng, “Engineering Auger recombination in colloidal quantum dots via dielectric screening,” Nat. Commun. 10(1), 1750 (2019).
[Crossref]

Chen, Z.

Chepic, D. I.

D. I. Chepic, Al. L. Efros, A. I. Ekimov, M. G. Ivanov, V. A. Kharchenko, I. A. Kudriavtsev, and T. V. Yazeva, “Auger ionization of semiconductor quantum drops in a glass matrix,” J. Lumin. 47(3), 113–127 (1990).
[Crossref]

Chung, S. Y.

E. Lerner, T. Cordes, A. Ingargiola, Y. Alhadid, S. Y. Chung, X. Michalet, and S. Weiss, “Toward dynamic structural biology: two decades of singer-molexule Förster resonance energy transfer,” Science359(6373), eaan1133 (2018).
[Crossref]

Cicek, N.

Clapp, A. R.

A. R. Clapp, T. Pons, I. L. Medintz, J. B. Delehanty, J. S. Melinger, T. Tiefenbrunn, P. E. Dawson, B. R. Fisher, B. O’Rourke, and H. Mattoussi, “Two-photon excitation of quantum-dot-based fluorescence resonance energy transfer and its applications,” Adv. Mater. 19(15), 1921–1926 (2007).
[Crossref]

A. R. Clapp, I. L. Medintz, J. M. Mauro, B. R. Fisher, M. G. Bawendi, and H. Mattoussi, “Fluorescence resonance energy transfer between quantum dot donors and dye-labeled protein acceptors,” J. Am. Chem. Soc. 126(1), 301–310 (2004).
[Crossref]

Cohen, E.

E. Cohen, P. Komm, N. Rosenthal-Strauss, J. Dehnel, E. Lifshitz, S. Yochelis, R. D. Levine, F. Remacle, B. Fresch, G. Marcus, and Y. Paltiel, “Fast energy transfer in cdse quantum dot layered structures: controlling coupling with covalent-bond organic linkers,” J. Phys. Chem. C 122(10), 5753–5758 (2018).
[Crossref]

Cordes, T.

E. Lerner, T. Cordes, A. Ingargiola, Y. Alhadid, S. Y. Chung, X. Michalet, and S. Weiss, “Toward dynamic structural biology: two decades of singer-molexule Förster resonance energy transfer,” Science359(6373), eaan1133 (2018).
[Crossref]

Cragg, G. E.

G. E. Cragg and A. L. Efros, “Suppression of Auger processes in confined structures,” Nano Lett. 10(1), 313–317 (2010).
[Crossref]

Crooker, S. A.

F. Garcia-Santamaria, S. Brovelli, R. Viswanatha, J. A. Hollingsworth, H. Htoon, S. A. Crooker, and V. I. Klimov, “Breakdown of volume scaling in Auger recombination in cdse/cds heteronanocrystals: the role of the core-shell interface,” Nano Lett. 11(2), 687–693 (2011).
[Crossref]

Dawson, P. E.

A. R. Clapp, T. Pons, I. L. Medintz, J. B. Delehanty, J. S. Melinger, T. Tiefenbrunn, P. E. Dawson, B. R. Fisher, B. O’Rourke, and H. Mattoussi, “Two-photon excitation of quantum-dot-based fluorescence resonance energy transfer and its applications,” Adv. Mater. 19(15), 1921–1926 (2007).
[Crossref]

de Torres, J.

P. Ghenuche, M. Mivelle, J. de Torres, S. B. Moparthi, H. Rigneault, N. F. V. Hulst, M. F. G. Parajó, and J. Wenger, “Matching nanoantenna field confinement to FRET distances enhances Förster energy transfer rates,” Nano Lett. 15(9), 6193–6201 (2015).
[Crossref]

Dehnel, J.

E. Cohen, P. Komm, N. Rosenthal-Strauss, J. Dehnel, E. Lifshitz, S. Yochelis, R. D. Levine, F. Remacle, B. Fresch, G. Marcus, and Y. Paltiel, “Fast energy transfer in cdse quantum dot layered structures: controlling coupling with covalent-bond organic linkers,” J. Phys. Chem. C 122(10), 5753–5758 (2018).
[Crossref]

Delehanty, J. B.

A. R. Clapp, T. Pons, I. L. Medintz, J. B. Delehanty, J. S. Melinger, T. Tiefenbrunn, P. E. Dawson, B. R. Fisher, B. O’Rourke, and H. Mattoussi, “Two-photon excitation of quantum-dot-based fluorescence resonance energy transfer and its applications,” Adv. Mater. 19(15), 1921–1926 (2007).
[Crossref]

Demir, H. V.

Deng, W. Q.

B. Yang, J. S. Chen, S. Q. Yang, F. Hong, L. Sun, P. G. Han, T. Pullerits, W. Q. Deng, and K. L. Han, “Lead-free silver-bismuth halide double perovskite nanocrystals,” Angew. Chem. Int. Ed. 57(19), 5359–5363 (2018).
[Crossref]

Ding, D.

Ding, D. J.

H.F. Zhao, H. Yin, X. C. Liu, H. Li, Y. Shi, C. L. Liu, M. X. Jin, J. B. Gao, Y. Luo, and D. J. Ding, “Pressure-induced tunable electron transfer and Auger recombination rates in cdse/zns quantum dot–anthraquinone complexes,” J. Phys. Chem. Lett. 10(11), 3064–3070 (2019).
[Crossref]

Dworak, L.

L. Dworak, V. V. Matylitsky, T. Ren, T. Basche, and J. Wachtveitl, “Acceptor concentration dependence of Förster resonance energy transfer dynamics in dye-quantum dot complexes,” J. Phys. Chem. C 118(8), 4396–4402 (2014).
[Crossref]

Dzhagan, V. M.

V. M. Dzhagan, M. Y. Valakh, A. E. Raevskaya, A. L. Stroyuk, S. Y. Kuchmiy, and D. R. T. Zahn, “Resonant raman scattering study of cdse nanocrystals passivated with cds and zns,” Nanotechnology 18(28), 285701 (2007).
[Crossref]

Efros, A. L.

R. Vaxenburg, A. Rodina, A. Shabaev, E. Lifshitz, and A. L. Efros, “Nonradiative Auger recombination in semiconductor nanocrystals,” Nano Lett. 15(3), 2092–2098 (2015).
[Crossref]

G. E. Cragg and A. L. Efros, “Suppression of Auger processes in confined structures,” Nano Lett. 10(1), 313–317 (2010).
[Crossref]

Efros, Al. L.

D. I. Chepic, Al. L. Efros, A. I. Ekimov, M. G. Ivanov, V. A. Kharchenko, I. A. Kudriavtsev, and T. V. Yazeva, “Auger ionization of semiconductor quantum drops in a glass matrix,” J. Lumin. 47(3), 113–127 (1990).
[Crossref]

Ekimov, A. I.

D. I. Chepic, Al. L. Efros, A. I. Ekimov, M. G. Ivanov, V. A. Kharchenko, I. A. Kudriavtsev, and T. V. Yazeva, “Auger ionization of semiconductor quantum drops in a glass matrix,” J. Lumin. 47(3), 113–127 (1990).
[Crossref]

Emery, B.

L. L. Wu, C. S. Huang, B. Emery, A. C. Sedgwick, S. D. Bull, X. P. He, H. Tian, J. Yoon, J. L. Sessler, and T. D. James, “Förster resonance energy transfer (FRET)-based small-molecule sensors and imaging agents,” Chem. Soc. Rev. 49(15), 5110–5139 (2020).
[Crossref]

Eychmüller, A.

E. Mutlugun, O. Samarskaya, T. Ozel, N. Cicek, N. Gaponik, A. Eychmüller, and H. V. Demir, “Highly efficient nonradiative energy transfer mediated light harvesting in water using aqueous CdTe quantum dot antennas,” Opt. Express 18(10), 10720–10730 (2010).
[Crossref]

T. Franzl, A. Shavel, A. L. Rogach, N. Gaponik, T. A. Klar, A. Eychmüller, and J. Feldmann, “High-rate unidirectional energy transfer in directly assembled cdte nanocrystal bilayers,” Small 1(4), 392–395 (2005).
[Crossref]

Fan, H.

F. Bai, K. Bian, X. Huang, Z. Wang, and H. Fan, “Pressure induced nanoparticle phase behavior, property, and applications,” Chem. Rev. 119(12), 7673–7717 (2019).
[Crossref]

Fedin, I.

C. E. Rowland, I. Fedin, H. Zhang, S. K. Gray, A. O. Govorov, D. V. Talapin, and R. D. Schaller, “Picosecond energy transfer and multiexciton transfer outpaces Auger recombination in binary cdse nanoplatelet solids,” Nature Mater 14(5), 484–489 (2015).
[Crossref]

Feldmann, J.

T. Franzl, A. Shavel, A. L. Rogach, N. Gaponik, T. A. Klar, A. Eychmüller, and J. Feldmann, “High-rate unidirectional energy transfer in directly assembled cdte nanocrystal bilayers,” Small 1(4), 392–395 (2005).
[Crossref]

Fidler, A. F.

J. M. Pietryga, Y. S. Park, J. Lim, A. F. Fidler, W. K. Bae, S. Brovelli, and V. I. Klimov, “Spectroscopic and device aspects of nanocrystal quantum dots,” Chem. Rev. 116(18), 10513–10622 (2016).
[Crossref]

Fisher, B. R.

A. R. Clapp, T. Pons, I. L. Medintz, J. B. Delehanty, J. S. Melinger, T. Tiefenbrunn, P. E. Dawson, B. R. Fisher, B. O’Rourke, and H. Mattoussi, “Two-photon excitation of quantum-dot-based fluorescence resonance energy transfer and its applications,” Adv. Mater. 19(15), 1921–1926 (2007).
[Crossref]

A. R. Clapp, I. L. Medintz, J. M. Mauro, B. R. Fisher, M. G. Bawendi, and H. Mattoussi, “Fluorescence resonance energy transfer between quantum dot donors and dye-labeled protein acceptors,” J. Am. Chem. Soc. 126(1), 301–310 (2004).
[Crossref]

Franzl, T.

T. Franzl, A. Shavel, A. L. Rogach, N. Gaponik, T. A. Klar, A. Eychmüller, and J. Feldmann, “High-rate unidirectional energy transfer in directly assembled cdte nanocrystal bilayers,” Small 1(4), 392–395 (2005).
[Crossref]

Frederick, M. T.

A. J. Morris-Cohen, M. T. Frederick, L. C. Cass, and E. A. Weiss, “Simultaneous determination of the adsorption constant and the photoinduced electron transfer rate for a cds quantum dot-violagen complex,” J. Am. Chem. Soc. 133(26), 10146–10154 (2011).
[Crossref]

Fresch, B.

E. Cohen, P. Komm, N. Rosenthal-Strauss, J. Dehnel, E. Lifshitz, S. Yochelis, R. D. Levine, F. Remacle, B. Fresch, G. Marcus, and Y. Paltiel, “Fast energy transfer in cdse quantum dot layered structures: controlling coupling with covalent-bond organic linkers,” J. Phys. Chem. C 122(10), 5753–5758 (2018).
[Crossref]

Gao, J.

J. Gao, H. Zhang, X. Liu, N. Zhou, X. Pi, D. Li, and D. Yang, “Plasmon-coupled Förster resonance energy transfer between silicon quantim dots,” J. Phys. Chem. C 123(38), 23604–23609 (2019).
[Crossref]

J. Gao, S. C. Nguyen, N. D. Bronstein, and A. P. Alivisatos, “Solution-processed, high-speed, and high-quantum-efficiency quantum dot infrared photodetectors,” ACS Photonics 3(7), 1217–1222 (2016).
[Crossref]

Gao, J. B.

H.F. Zhao, H. Yin, X. C. Liu, H. Li, Y. Shi, C. L. Liu, M. X. Jin, J. B. Gao, Y. Luo, and D. J. Ding, “Pressure-induced tunable electron transfer and Auger recombination rates in cdse/zns quantum dot–anthraquinone complexes,” J. Phys. Chem. Lett. 10(11), 3064–3070 (2019).
[Crossref]

Gao, Y. C.

Gaponik, N.

E. Mutlugun, O. Samarskaya, T. Ozel, N. Cicek, N. Gaponik, A. Eychmüller, and H. V. Demir, “Highly efficient nonradiative energy transfer mediated light harvesting in water using aqueous CdTe quantum dot antennas,” Opt. Express 18(10), 10720–10730 (2010).
[Crossref]

T. Franzl, A. Shavel, A. L. Rogach, N. Gaponik, T. A. Klar, A. Eychmüller, and J. Feldmann, “High-rate unidirectional energy transfer in directly assembled cdte nanocrystal bilayers,” Small 1(4), 392–395 (2005).
[Crossref]

Garcia-Santamaria, F.

F. Garcia-Santamaria, S. Brovelli, R. Viswanatha, J. A. Hollingsworth, H. Htoon, S. A. Crooker, and V. I. Klimov, “Breakdown of volume scaling in Auger recombination in cdse/cds heteronanocrystals: the role of the core-shell interface,” Nano Lett. 11(2), 687–693 (2011).
[Crossref]

Ghenuche, P.

P. Ghenuche, M. Mivelle, J. de Torres, S. B. Moparthi, H. Rigneault, N. F. V. Hulst, M. F. G. Parajó, and J. Wenger, “Matching nanoantenna field confinement to FRET distances enhances Förster energy transfer rates,” Nano Lett. 15(9), 6193–6201 (2015).
[Crossref]

Govorov, A. O.

S. Panuganti, L. V. Besteiro, E. S. Vasileiadou, J. M. Hoffman, A. O. Govorov, S. K. Gray, M. G. Kanatzidis, and R. D. Schaller, “Distance dependence of Förster resonance energy transfer rates in 2D perovskite quantum wells via control of organic spacer length,” J. Am. Chem. Soc. 143(11), 4244–4252 (2021).
[Crossref]

C. E. Rowland, I. Fedin, H. Zhang, S. K. Gray, A. O. Govorov, D. V. Talapin, and R. D. Schaller, “Picosecond energy transfer and multiexciton transfer outpaces Auger recombination in binary cdse nanoplatelet solids,” Nature Mater 14(5), 484–489 (2015).
[Crossref]

Gradecak, S.

S. Q. Ren, L. Y. Chang, S. K. Lim, J. Zhao, M. Smith, N. Zhao, V. Bulovic, M. Bawendi, and S. Gradecak, “Inorganic-organic hybrid solar cell: bridging quantum dots to conjugated polymer nanowires,” Nano Lett. 11(9), 3998–4002 (2011).
[Crossref]

Gray, S. K.

S. Panuganti, L. V. Besteiro, E. S. Vasileiadou, J. M. Hoffman, A. O. Govorov, S. K. Gray, M. G. Kanatzidis, and R. D. Schaller, “Distance dependence of Förster resonance energy transfer rates in 2D perovskite quantum wells via control of organic spacer length,” J. Am. Chem. Soc. 143(11), 4244–4252 (2021).
[Crossref]

C. E. Rowland, I. Fedin, H. Zhang, S. K. Gray, A. O. Govorov, D. V. Talapin, and R. D. Schaller, “Picosecond energy transfer and multiexciton transfer outpaces Auger recombination in binary cdse nanoplatelet solids,” Nature Mater 14(5), 484–489 (2015).
[Crossref]

Guo, W.

W. Guo, J. Tang, G. Zhang, B. Li, C. Yang, R. Chen, C. Qin, J. Hu, H. Zhong, L. Xiao, and S. Jia, “Photoluminescence blinking and biexcition Auger recombination in single colloidal quantum dots with sharp and smooth core/shell interfaces,” J. Phys. Chem. Lett. 12(1), 405–412 (2021).
[Crossref]

Guyer, J. E.

J. E. Guyer and P. W. Voorhees, “Morphological stability of alloy thin films,” Phys. Rev. Lett. 74(20), 4031–4034 (1995).
[Crossref]

Han, J.

Han, K. L.

B. Yang, J. S. Chen, S. Q. Yang, F. Hong, L. Sun, P. G. Han, T. Pullerits, W. Q. Deng, and K. L. Han, “Lead-free silver-bismuth halide double perovskite nanocrystals,” Angew. Chem. Int. Ed. 57(19), 5359–5363 (2018).
[Crossref]

Han, P. G.

B. Yang, J. S. Chen, S. Q. Yang, F. Hong, L. Sun, P. G. Han, T. Pullerits, W. Q. Deng, and K. L. Han, “Lead-free silver-bismuth halide double perovskite nanocrystals,” Angew. Chem. Int. Ed. 57(19), 5359–5363 (2018).
[Crossref]

He, X. P.

L. L. Wu, C. S. Huang, B. Emery, A. C. Sedgwick, S. D. Bull, X. P. He, H. Tian, J. Yoon, J. L. Sessler, and T. D. James, “Förster resonance energy transfer (FRET)-based small-molecule sensors and imaging agents,” Chem. Soc. Rev. 49(15), 5110–5139 (2020).
[Crossref]

Hildebrandt, N.

M. Cardoso Dos Santos, W. R. Algar, I. L. Medintz, and N. Hildebrandt, “Quantum dots for Förster resonance energy transfer (FRET),” Trends Anal. Chem. 125, 115819 (2020).
[Crossref]

Hirsch, T.

V. Muhr, C. Wurth, M. Kraft, M. Buchner, A. J. Baeumner, U. Resch-Genger, and T. Hirsch, “Particle-size-dependent Förster resonance energy transfer from upconversion nanoparticles to organic dyes,” Anal. Chem. 89(9), 4868–4874 (2017).
[Crossref]

Hoffman, J. M.

S. Panuganti, L. V. Besteiro, E. S. Vasileiadou, J. M. Hoffman, A. O. Govorov, S. K. Gray, M. G. Kanatzidis, and R. D. Schaller, “Distance dependence of Förster resonance energy transfer rates in 2D perovskite quantum wells via control of organic spacer length,” J. Am. Chem. Soc. 143(11), 4244–4252 (2021).
[Crossref]

Hollingsworth, J. A.

F. Garcia-Santamaria, S. Brovelli, R. Viswanatha, J. A. Hollingsworth, H. Htoon, S. A. Crooker, and V. I. Klimov, “Breakdown of volume scaling in Auger recombination in cdse/cds heteronanocrystals: the role of the core-shell interface,” Nano Lett. 11(2), 687–693 (2011).
[Crossref]

Hong, F.

B. Yang, J. S. Chen, S. Q. Yang, F. Hong, L. Sun, P. G. Han, T. Pullerits, W. Q. Deng, and K. L. Han, “Lead-free silver-bismuth halide double perovskite nanocrystals,” Angew. Chem. Int. Ed. 57(19), 5359–5363 (2018).
[Crossref]

Hou, X.

X. Hou, J. Kang, H. Qin, X. Chen, J. Ma, J. Zhou, L. Chen, L. Wang, L-W. Wang, and X. Peng, “Engineering Auger recombination in colloidal quantum dots via dielectric screening,” Nat. Commun. 10(1), 1750 (2019).
[Crossref]

Htoon, H.

F. Garcia-Santamaria, S. Brovelli, R. Viswanatha, J. A. Hollingsworth, H. Htoon, S. A. Crooker, and V. I. Klimov, “Breakdown of volume scaling in Auger recombination in cdse/cds heteronanocrystals: the role of the core-shell interface,” Nano Lett. 11(2), 687–693 (2011).
[Crossref]

Hu, J.

W. Guo, J. Tang, G. Zhang, B. Li, C. Yang, R. Chen, C. Qin, J. Hu, H. Zhong, L. Xiao, and S. Jia, “Photoluminescence blinking and biexcition Auger recombination in single colloidal quantum dots with sharp and smooth core/shell interfaces,” J. Phys. Chem. Lett. 12(1), 405–412 (2021).
[Crossref]

Huang, B.C.

B.C. Huang, L. Xu, J. L. Zhu, Y. X. Wang, B. Sun, X. P. Li, and H. B. Yang, “Real-time monitoring the dynamics of coordination-driven self-assembly by fluorescence-resonance energy transfer,” J. Am. Chem. Soc. 139(28), 9459–9462 (2017).
[Crossref]

Huang, C. S.

L. L. Wu, C. S. Huang, B. Emery, A. C. Sedgwick, S. D. Bull, X. P. He, H. Tian, J. Yoon, J. L. Sessler, and T. D. James, “Förster resonance energy transfer (FRET)-based small-molecule sensors and imaging agents,” Chem. Soc. Rev. 49(15), 5110–5139 (2020).
[Crossref]

Huang, X.

F. Bai, K. Bian, X. Huang, Z. Wang, and H. Fan, “Pressure induced nanoparticle phase behavior, property, and applications,” Chem. Rev. 119(12), 7673–7717 (2019).
[Crossref]

Hulst, N. F. V.

P. Ghenuche, M. Mivelle, J. de Torres, S. B. Moparthi, H. Rigneault, N. F. V. Hulst, M. F. G. Parajó, and J. Wenger, “Matching nanoantenna field confinement to FRET distances enhances Förster energy transfer rates,” Nano Lett. 15(9), 6193–6201 (2015).
[Crossref]

Ingargiola, A.

E. Lerner, T. Cordes, A. Ingargiola, Y. Alhadid, S. Y. Chung, X. Michalet, and S. Weiss, “Toward dynamic structural biology: two decades of singer-molexule Förster resonance energy transfer,” Science359(6373), eaan1133 (2018).
[Crossref]

Ivanov, M. G.

D. I. Chepic, Al. L. Efros, A. I. Ekimov, M. G. Ivanov, V. A. Kharchenko, I. A. Kudriavtsev, and T. V. Yazeva, “Auger ionization of semiconductor quantum drops in a glass matrix,” J. Lumin. 47(3), 113–127 (1990).
[Crossref]

James, T. D.

L. L. Wu, C. S. Huang, B. Emery, A. C. Sedgwick, S. D. Bull, X. P. He, H. Tian, J. Yoon, J. L. Sessler, and T. D. James, “Förster resonance energy transfer (FRET)-based small-molecule sensors and imaging agents,” Chem. Soc. Rev. 49(15), 5110–5139 (2020).
[Crossref]

Jana, S.

S. Jana, X. Xu, A. Klymchenko, A. Reisch, and T. Pons, “Microcavity-enhanced fluorescence energy transfer from quantum dot excited whispering gallery modes to acceptor dye nanoparticles,” ACS Nano 15(1), 1445–1453 (2021).
[Crossref]

Jia, S.

W. Guo, J. Tang, G. Zhang, B. Li, C. Yang, R. Chen, C. Qin, J. Hu, H. Zhong, L. Xiao, and S. Jia, “Photoluminescence blinking and biexcition Auger recombination in single colloidal quantum dots with sharp and smooth core/shell interfaces,” J. Phys. Chem. Lett. 12(1), 405–412 (2021).
[Crossref]

Jin, M.

Jin, M. X.

H.F. Zhao, H. Yin, X. C. Liu, H. Li, Y. Shi, C. L. Liu, M. X. Jin, J. B. Gao, Y. Luo, and D. J. Ding, “Pressure-induced tunable electron transfer and Auger recombination rates in cdse/zns quantum dot–anthraquinone complexes,” J. Phys. Chem. Lett. 10(11), 3064–3070 (2019).
[Crossref]

Jin, T.

W. Bi, X. Li, L. Zhang, T. Jin, L. Zhang, Q. Zhang, Y. Luo, C. Wu, and Y. Xie, “Molecular co-catalyst accelerating hole transfer for enhanced photocatalytic H2 evolution,” Nat. Commun. 6(1), 8647 (2015).
[Crossref]

Kanatzidis, M. G.

S. Panuganti, L. V. Besteiro, E. S. Vasileiadou, J. M. Hoffman, A. O. Govorov, S. K. Gray, M. G. Kanatzidis, and R. D. Schaller, “Distance dependence of Förster resonance energy transfer rates in 2D perovskite quantum wells via control of organic spacer length,” J. Am. Chem. Soc. 143(11), 4244–4252 (2021).
[Crossref]

Kang, J.

X. Hou, J. Kang, H. Qin, X. Chen, J. Ma, J. Zhou, L. Chen, L. Wang, L-W. Wang, and X. Peng, “Engineering Auger recombination in colloidal quantum dots via dielectric screening,” Nat. Commun. 10(1), 1750 (2019).
[Crossref]

Kharchenko, V. A.

D. I. Chepic, Al. L. Efros, A. I. Ekimov, M. G. Ivanov, V. A. Kharchenko, I. A. Kudriavtsev, and T. V. Yazeva, “Auger ionization of semiconductor quantum drops in a glass matrix,” J. Lumin. 47(3), 113–127 (1990).
[Crossref]

Klar, T. A.

T. Franzl, A. Shavel, A. L. Rogach, N. Gaponik, T. A. Klar, A. Eychmüller, and J. Feldmann, “High-rate unidirectional energy transfer in directly assembled cdte nanocrystal bilayers,” Small 1(4), 392–395 (2005).
[Crossref]

Klimov, V. I.

Y. S. Park, J. Lim, N. S. Makarov, and V. I. Klimov, “Effect of interfacial alloying versus “volume scaling” on Auger recombination in compositionally graded semiconductor quantum dots,” Nano Lett. 17(9), 5607–5613 (2017).
[Crossref]

J. M. Pietryga, Y. S. Park, J. Lim, A. F. Fidler, W. K. Bae, S. Brovelli, and V. I. Klimov, “Spectroscopic and device aspects of nanocrystal quantum dots,” Chem. Rev. 116(18), 10513–10622 (2016).
[Crossref]

V. I. Klimov, “Multicarrier interactions in semiconductor nanocrystals in relation to the phenomena of Auger recombination and carrier multiplication,” Annu. Rev. Condens. Matter Phys. 5(1), 285–316 (2014).
[Crossref]

Y. S. Park, W. K. Bae, L. A. Padilha, J. M. Pietryga, and V. I. Klimov, “Effect of the core/shell interface on Auger recombination evaluated by single-quantum-dot spectroscopy,” Nano Lett. 14(2), 396–402 (2014).
[Crossref]

W. K. Bae, L. A. Padilha, Y. S. Park, H. McDaniel, I. Robel, J. M. Pietryga, and V. I. Klimov, “Controlled alloying of the core-shell interface in cdse/cds quantum dots for suppression of Auger recombination,” ACS Nano 7(4), 3411–3419 (2013).
[Crossref]

W. K. Bae, Y. S. Park, J. Lim, D. Lee, L. A. Padilha, H. McDaniel, I. Robel, C. Lee, J. M. Pietryga, and V. I. Klimov, “Controlling the influence of Auger recombination on the performance of quantum-dot light-emitting diodes,” Nat. Commun. 4(1), 2661 (2013).
[Crossref]

F. Garcia-Santamaria, S. Brovelli, R. Viswanatha, J. A. Hollingsworth, H. Htoon, S. A. Crooker, and V. I. Klimov, “Breakdown of volume scaling in Auger recombination in cdse/cds heteronanocrystals: the role of the core-shell interface,” Nano Lett. 11(2), 687–693 (2011).
[Crossref]

V. I. Klimov, A. A. Mikhailovsky, D. W. Mcbranch, C. A. Leatherdale, and M. G. Bawendi, “Quantization of multiparticle Auger rates in semiconductor quantum dots,” Science 287(5455), 1011–1013 (2000).
[Crossref]

Klymchenko, A.

S. Jana, X. Xu, A. Klymchenko, A. Reisch, and T. Pons, “Microcavity-enhanced fluorescence energy transfer from quantum dot excited whispering gallery modes to acceptor dye nanoparticles,” ACS Nano 15(1), 1445–1453 (2021).
[Crossref]

Komm, P.

E. Cohen, P. Komm, N. Rosenthal-Strauss, J. Dehnel, E. Lifshitz, S. Yochelis, R. D. Levine, F. Remacle, B. Fresch, G. Marcus, and Y. Paltiel, “Fast energy transfer in cdse quantum dot layered structures: controlling coupling with covalent-bond organic linkers,” J. Phys. Chem. C 122(10), 5753–5758 (2018).
[Crossref]

Kong, D. G.

Kraft, M.

V. Muhr, C. Wurth, M. Kraft, M. Buchner, A. J. Baeumner, U. Resch-Genger, and T. Hirsch, “Particle-size-dependent Förster resonance energy transfer from upconversion nanoparticles to organic dyes,” Anal. Chem. 89(9), 4868–4874 (2017).
[Crossref]

Kuchmiy, S. Y.

V. M. Dzhagan, M. Y. Valakh, A. E. Raevskaya, A. L. Stroyuk, S. Y. Kuchmiy, and D. R. T. Zahn, “Resonant raman scattering study of cdse nanocrystals passivated with cds and zns,” Nanotechnology 18(28), 285701 (2007).
[Crossref]

Kudriavtsev, I. A.

D. I. Chepic, Al. L. Efros, A. I. Ekimov, M. G. Ivanov, V. A. Kharchenko, I. A. Kudriavtsev, and T. V. Yazeva, “Auger ionization of semiconductor quantum drops in a glass matrix,” J. Lumin. 47(3), 113–127 (1990).
[Crossref]

Leatherdale, C. A.

V. I. Klimov, A. A. Mikhailovsky, D. W. Mcbranch, C. A. Leatherdale, and M. G. Bawendi, “Quantization of multiparticle Auger rates in semiconductor quantum dots,” Science 287(5455), 1011–1013 (2000).
[Crossref]

Lee, C.

W. K. Bae, Y. S. Park, J. Lim, D. Lee, L. A. Padilha, H. McDaniel, I. Robel, C. Lee, J. M. Pietryga, and V. I. Klimov, “Controlling the influence of Auger recombination on the performance of quantum-dot light-emitting diodes,” Nat. Commun. 4(1), 2661 (2013).
[Crossref]

Lee, D.

W. K. Bae, Y. S. Park, J. Lim, D. Lee, L. A. Padilha, H. McDaniel, I. Robel, C. Lee, J. M. Pietryga, and V. I. Klimov, “Controlling the influence of Auger recombination on the performance of quantum-dot light-emitting diodes,” Nat. Commun. 4(1), 2661 (2013).
[Crossref]

Lei, H.

Lerner, E.

E. Lerner, T. Cordes, A. Ingargiola, Y. Alhadid, S. Y. Chung, X. Michalet, and S. Weiss, “Toward dynamic structural biology: two decades of singer-molexule Förster resonance energy transfer,” Science359(6373), eaan1133 (2018).
[Crossref]

Levine, R. D.

E. Cohen, P. Komm, N. Rosenthal-Strauss, J. Dehnel, E. Lifshitz, S. Yochelis, R. D. Levine, F. Remacle, B. Fresch, G. Marcus, and Y. Paltiel, “Fast energy transfer in cdse quantum dot layered structures: controlling coupling with covalent-bond organic linkers,” J. Phys. Chem. C 122(10), 5753–5758 (2018).
[Crossref]

Li, B.

W. Guo, J. Tang, G. Zhang, B. Li, C. Yang, R. Chen, C. Qin, J. Hu, H. Zhong, L. Xiao, and S. Jia, “Photoluminescence blinking and biexcition Auger recombination in single colloidal quantum dots with sharp and smooth core/shell interfaces,” J. Phys. Chem. Lett. 12(1), 405–412 (2021).
[Crossref]

W. Zhang, J. Li, H. Lei, and B. Li, “Temperature-dependent Förster resonance energy transfer from upconversion nanoparticles to quantum dots,” Opt. Express 28(8), 12450–12459 (2020).
[Crossref]

Li, D.

J. Gao, H. Zhang, X. Liu, N. Zhou, X. Pi, D. Li, and D. Yang, “Plasmon-coupled Förster resonance energy transfer between silicon quantim dots,” J. Phys. Chem. C 123(38), 23604–23609 (2019).
[Crossref]

Li, H.

H.F. Zhao, H. Yin, X. C. Liu, H. Li, Y. Shi, C. L. Liu, M. X. Jin, J. B. Gao, Y. Luo, and D. J. Ding, “Pressure-induced tunable electron transfer and Auger recombination rates in cdse/zns quantum dot–anthraquinone complexes,” J. Phys. Chem. Lett. 10(11), 3064–3070 (2019).
[Crossref]

Li, H. Y.

Li, J.

W. Zhang, J. Li, H. Lei, and B. Li, “Temperature-dependent Förster resonance energy transfer from upconversion nanoparticles to quantum dots,” Opt. Express 28(8), 12450–12459 (2020).
[Crossref]

H. Zong, J. Wang, X. Mu, X. Xu, J. Li, X. Wang, F. Long, J. Wang, and M. Sun, “Physical mechanism of photoinduced intermolecular charge transfer enhanced by fluorescence resonance energy transfer,” Phys. Chem. Chem. Phys. 20(19), 13558–13565 (2018).
[Crossref]

Li, Q. H.

Li, X.

W. Bi, X. Li, L. Zhang, T. Jin, L. Zhang, Q. Zhang, Y. Luo, C. Wu, and Y. Xie, “Molecular co-catalyst accelerating hole transfer for enhanced photocatalytic H2 evolution,” Nat. Commun. 6(1), 8647 (2015).
[Crossref]

Li, X. P.

B.C. Huang, L. Xu, J. L. Zhu, Y. X. Wang, B. Sun, X. P. Li, and H. B. Yang, “Real-time monitoring the dynamics of coordination-driven self-assembly by fluorescence-resonance energy transfer,” J. Am. Chem. Soc. 139(28), 9459–9462 (2017).
[Crossref]

Li, Y.

Li, Y. L.

Y. L. Li and K. F. Wu, “Size and halide dependent Auger recombination in lead halide perovskite nanocrystals,” Angew. Chem. Int. Edit. 59(34), 14292–14295 (2020).
[Crossref]

Lian, T.

H. Zhu, N. Song, and T. Lian, “Controlling charge separation and recombination rates in cdse/zns type I core−shell quantum dots by shell thicknesses,” J. Am. Chem. Soc. 132(42), 15038–15045 (2010).
[Crossref]

Liang, G.

Liang, Y.

Lifshitz, E.

E. Cohen, P. Komm, N. Rosenthal-Strauss, J. Dehnel, E. Lifshitz, S. Yochelis, R. D. Levine, F. Remacle, B. Fresch, G. Marcus, and Y. Paltiel, “Fast energy transfer in cdse quantum dot layered structures: controlling coupling with covalent-bond organic linkers,” J. Phys. Chem. C 122(10), 5753–5758 (2018).
[Crossref]

R. Vaxenburg, A. Rodina, A. Shabaev, E. Lifshitz, and A. L. Efros, “Nonradiative Auger recombination in semiconductor nanocrystals,” Nano Lett. 15(3), 2092–2098 (2015).
[Crossref]

Lim, J.

Y. S. Park, J. Lim, N. S. Makarov, and V. I. Klimov, “Effect of interfacial alloying versus “volume scaling” on Auger recombination in compositionally graded semiconductor quantum dots,” Nano Lett. 17(9), 5607–5613 (2017).
[Crossref]

J. M. Pietryga, Y. S. Park, J. Lim, A. F. Fidler, W. K. Bae, S. Brovelli, and V. I. Klimov, “Spectroscopic and device aspects of nanocrystal quantum dots,” Chem. Rev. 116(18), 10513–10622 (2016).
[Crossref]

W. K. Bae, Y. S. Park, J. Lim, D. Lee, L. A. Padilha, H. McDaniel, I. Robel, C. Lee, J. M. Pietryga, and V. I. Klimov, “Controlling the influence of Auger recombination on the performance of quantum-dot light-emitting diodes,” Nat. Commun. 4(1), 2661 (2013).
[Crossref]

Lim, S. K.

S. Q. Ren, L. Y. Chang, S. K. Lim, J. Zhao, M. Smith, N. Zhao, V. Bulovic, M. Bawendi, and S. Gradecak, “Inorganic-organic hybrid solar cell: bridging quantum dots to conjugated polymer nanowires,” Nano Lett. 11(9), 3998–4002 (2011).
[Crossref]

Liu, C.

Liu, C. L.

H.F. Zhao, H. Yin, X. C. Liu, H. Li, Y. Shi, C. L. Liu, M. X. Jin, J. B. Gao, Y. Luo, and D. J. Ding, “Pressure-induced tunable electron transfer and Auger recombination rates in cdse/zns quantum dot–anthraquinone complexes,” J. Phys. Chem. Lett. 10(11), 3064–3070 (2019).
[Crossref]

Liu, D.

Liu, X.

X. Liu, J. Han, Y. Li, B. Cao, C. Sun, H. Yin, Y. Shi, M. Jin, C. Liu, M. Sun, and D. Ding, “Ultrafast carrier dynamics in all-inorganic CsPbBr3 perovskite across the pressure-induced phase transition,” Opt. Express 27(16), A995–1003 (2019).
[Crossref]

J. Gao, H. Zhang, X. Liu, N. Zhou, X. Pi, D. Li, and D. Yang, “Plasmon-coupled Förster resonance energy transfer between silicon quantim dots,” J. Phys. Chem. C 123(38), 23604–23609 (2019).
[Crossref]

Liu, X. C.

H.F. Zhao, H. Yin, X. C. Liu, H. Li, Y. Shi, C. L. Liu, M. X. Jin, J. B. Gao, Y. Luo, and D. J. Ding, “Pressure-induced tunable electron transfer and Auger recombination rates in cdse/zns quantum dot–anthraquinone complexes,” J. Phys. Chem. Lett. 10(11), 3064–3070 (2019).
[Crossref]

Long, F.

H. Zong, J. Wang, X. Mu, X. Xu, J. Li, X. Wang, F. Long, J. Wang, and M. Sun, “Physical mechanism of photoinduced intermolecular charge transfer enhanced by fluorescence resonance energy transfer,” Phys. Chem. Chem. Phys. 20(19), 13558–13565 (2018).
[Crossref]

Luo, Y.

H.F. Zhao, H. Yin, X. C. Liu, H. Li, Y. Shi, C. L. Liu, M. X. Jin, J. B. Gao, Y. Luo, and D. J. Ding, “Pressure-induced tunable electron transfer and Auger recombination rates in cdse/zns quantum dot–anthraquinone complexes,” J. Phys. Chem. Lett. 10(11), 3064–3070 (2019).
[Crossref]

W. Bi, X. Li, L. Zhang, T. Jin, L. Zhang, Q. Zhang, Y. Luo, C. Wu, and Y. Xie, “Molecular co-catalyst accelerating hole transfer for enhanced photocatalytic H2 evolution,” Nat. Commun. 6(1), 8647 (2015).
[Crossref]

Ma, J.

X. Hou, J. Kang, H. Qin, X. Chen, J. Ma, J. Zhou, L. Chen, L. Wang, L-W. Wang, and X. Peng, “Engineering Auger recombination in colloidal quantum dots via dielectric screening,” Nat. Commun. 10(1), 1750 (2019).
[Crossref]

Makarov, N. S.

Y. S. Park, J. Lim, N. S. Makarov, and V. I. Klimov, “Effect of interfacial alloying versus “volume scaling” on Auger recombination in compositionally graded semiconductor quantum dots,” Nano Lett. 17(9), 5607–5613 (2017).
[Crossref]

Marcus, G.

E. Cohen, P. Komm, N. Rosenthal-Strauss, J. Dehnel, E. Lifshitz, S. Yochelis, R. D. Levine, F. Remacle, B. Fresch, G. Marcus, and Y. Paltiel, “Fast energy transfer in cdse quantum dot layered structures: controlling coupling with covalent-bond organic linkers,” J. Phys. Chem. C 122(10), 5753–5758 (2018).
[Crossref]

Mattoussi, H.

A. R. Clapp, T. Pons, I. L. Medintz, J. B. Delehanty, J. S. Melinger, T. Tiefenbrunn, P. E. Dawson, B. R. Fisher, B. O’Rourke, and H. Mattoussi, “Two-photon excitation of quantum-dot-based fluorescence resonance energy transfer and its applications,” Adv. Mater. 19(15), 1921–1926 (2007).
[Crossref]

A. R. Clapp, I. L. Medintz, J. M. Mauro, B. R. Fisher, M. G. Bawendi, and H. Mattoussi, “Fluorescence resonance energy transfer between quantum dot donors and dye-labeled protein acceptors,” J. Am. Chem. Soc. 126(1), 301–310 (2004).
[Crossref]

Matylitsky, V. V.

L. Dworak, V. V. Matylitsky, T. Ren, T. Basche, and J. Wachtveitl, “Acceptor concentration dependence of Förster resonance energy transfer dynamics in dye-quantum dot complexes,” J. Phys. Chem. C 118(8), 4396–4402 (2014).
[Crossref]

Mauro, J. M.

A. R. Clapp, I. L. Medintz, J. M. Mauro, B. R. Fisher, M. G. Bawendi, and H. Mattoussi, “Fluorescence resonance energy transfer between quantum dot donors and dye-labeled protein acceptors,” J. Am. Chem. Soc. 126(1), 301–310 (2004).
[Crossref]

Mcbranch, D. W.

V. I. Klimov, A. A. Mikhailovsky, D. W. Mcbranch, C. A. Leatherdale, and M. G. Bawendi, “Quantization of multiparticle Auger rates in semiconductor quantum dots,” Science 287(5455), 1011–1013 (2000).
[Crossref]

McDaniel, H.

W. K. Bae, L. A. Padilha, Y. S. Park, H. McDaniel, I. Robel, J. M. Pietryga, and V. I. Klimov, “Controlled alloying of the core-shell interface in cdse/cds quantum dots for suppression of Auger recombination,” ACS Nano 7(4), 3411–3419 (2013).
[Crossref]

W. K. Bae, Y. S. Park, J. Lim, D. Lee, L. A. Padilha, H. McDaniel, I. Robel, C. Lee, J. M. Pietryga, and V. I. Klimov, “Controlling the influence of Auger recombination on the performance of quantum-dot light-emitting diodes,” Nat. Commun. 4(1), 2661 (2013).
[Crossref]

Medintz, I. L.

M. Cardoso Dos Santos, W. R. Algar, I. L. Medintz, and N. Hildebrandt, “Quantum dots for Förster resonance energy transfer (FRET),” Trends Anal. Chem. 125, 115819 (2020).
[Crossref]

A. R. Clapp, T. Pons, I. L. Medintz, J. B. Delehanty, J. S. Melinger, T. Tiefenbrunn, P. E. Dawson, B. R. Fisher, B. O’Rourke, and H. Mattoussi, “Two-photon excitation of quantum-dot-based fluorescence resonance energy transfer and its applications,” Adv. Mater. 19(15), 1921–1926 (2007).
[Crossref]

K. E. Sapsford, L. Berti, and I. L. Medintz, “Materials for fluorescence resonance energy transfer analysis: beyond traditional donor–acceptor combinations,” Angew. Chem. Int. Ed. 45(28), 4562–4589 (2006).
[Crossref]

A. R. Clapp, I. L. Medintz, J. M. Mauro, B. R. Fisher, M. G. Bawendi, and H. Mattoussi, “Fluorescence resonance energy transfer between quantum dot donors and dye-labeled protein acceptors,” J. Am. Chem. Soc. 126(1), 301–310 (2004).
[Crossref]

Meijerink, A.

A. J. P. Teunissen, C. Pérez-Medina, A. Meijerink, and W. J. M. Mulder, “Investigating supramolecular systems using Förster resonance energy transfer,” Chem. Soc. Rev. 47(18), 7027–7044 (2018).
[Crossref]

Melinger, J. S.

A. R. Clapp, T. Pons, I. L. Medintz, J. B. Delehanty, J. S. Melinger, T. Tiefenbrunn, P. E. Dawson, B. R. Fisher, B. O’Rourke, and H. Mattoussi, “Two-photon excitation of quantum-dot-based fluorescence resonance energy transfer and its applications,” Adv. Mater. 19(15), 1921–1926 (2007).
[Crossref]

Michalet, X.

E. Lerner, T. Cordes, A. Ingargiola, Y. Alhadid, S. Y. Chung, X. Michalet, and S. Weiss, “Toward dynamic structural biology: two decades of singer-molexule Förster resonance energy transfer,” Science359(6373), eaan1133 (2018).
[Crossref]

Mikhailovsky, A. A.

V. I. Klimov, A. A. Mikhailovsky, D. W. Mcbranch, C. A. Leatherdale, and M. G. Bawendi, “Quantization of multiparticle Auger rates in semiconductor quantum dots,” Science 287(5455), 1011–1013 (2000).
[Crossref]

Mivelle, M.

P. Ghenuche, M. Mivelle, J. de Torres, S. B. Moparthi, H. Rigneault, N. F. V. Hulst, M. F. G. Parajó, and J. Wenger, “Matching nanoantenna field confinement to FRET distances enhances Förster energy transfer rates,” Nano Lett. 15(9), 6193–6201 (2015).
[Crossref]

Moparthi, S. B.

P. Ghenuche, M. Mivelle, J. de Torres, S. B. Moparthi, H. Rigneault, N. F. V. Hulst, M. F. G. Parajó, and J. Wenger, “Matching nanoantenna field confinement to FRET distances enhances Förster energy transfer rates,” Nano Lett. 15(9), 6193–6201 (2015).
[Crossref]

Morris-Cohen, A. J.

A. J. Morris-Cohen, M. T. Frederick, L. C. Cass, and E. A. Weiss, “Simultaneous determination of the adsorption constant and the photoinduced electron transfer rate for a cds quantum dot-violagen complex,” J. Am. Chem. Soc. 133(26), 10146–10154 (2011).
[Crossref]

Mu, X.

H. Zong, X. Mu, J. Wang, H. Zhao, Y. shi, and M. Sun, “The nature of photoinduced intermolecular charge transfer in fluorescence resonance energy transfer,” Spectrochim. Acta, Part A 209(15), 228–233 (2019).
[Crossref]

H. Zong, J. Wang, X. Mu, X. Xu, J. Li, X. Wang, F. Long, J. Wang, and M. Sun, “Physical mechanism of photoinduced intermolecular charge transfer enhanced by fluorescence resonance energy transfer,” Phys. Chem. Chem. Phys. 20(19), 13558–13565 (2018).
[Crossref]

Muhr, V.

V. Muhr, C. Wurth, M. Kraft, M. Buchner, A. J. Baeumner, U. Resch-Genger, and T. Hirsch, “Particle-size-dependent Förster resonance energy transfer from upconversion nanoparticles to organic dyes,” Anal. Chem. 89(9), 4868–4874 (2017).
[Crossref]

Mulder, W. J. M.

A. J. P. Teunissen, C. Pérez-Medina, A. Meijerink, and W. J. M. Mulder, “Investigating supramolecular systems using Förster resonance energy transfer,” Chem. Soc. Rev. 47(18), 7027–7044 (2018).
[Crossref]

Mutlugun, E.

Nguyen, S. C.

J. Gao, S. C. Nguyen, N. D. Bronstein, and A. P. Alivisatos, “Solution-processed, high-speed, and high-quantum-efficiency quantum dot infrared photodetectors,” ACS Photonics 3(7), 1217–1222 (2016).
[Crossref]

O’Rourke, B.

A. R. Clapp, T. Pons, I. L. Medintz, J. B. Delehanty, J. S. Melinger, T. Tiefenbrunn, P. E. Dawson, B. R. Fisher, B. O’Rourke, and H. Mattoussi, “Two-photon excitation of quantum-dot-based fluorescence resonance energy transfer and its applications,” Adv. Mater. 19(15), 1921–1926 (2007).
[Crossref]

Ozel, T.

Padilha, L. A.

Y. S. Park, W. K. Bae, L. A. Padilha, J. M. Pietryga, and V. I. Klimov, “Effect of the core/shell interface on Auger recombination evaluated by single-quantum-dot spectroscopy,” Nano Lett. 14(2), 396–402 (2014).
[Crossref]

W. K. Bae, Y. S. Park, J. Lim, D. Lee, L. A. Padilha, H. McDaniel, I. Robel, C. Lee, J. M. Pietryga, and V. I. Klimov, “Controlling the influence of Auger recombination on the performance of quantum-dot light-emitting diodes,” Nat. Commun. 4(1), 2661 (2013).
[Crossref]

W. K. Bae, L. A. Padilha, Y. S. Park, H. McDaniel, I. Robel, J. M. Pietryga, and V. I. Klimov, “Controlled alloying of the core-shell interface in cdse/cds quantum dots for suppression of Auger recombination,” ACS Nano 7(4), 3411–3419 (2013).
[Crossref]

Paltiel, Y.

E. Cohen, P. Komm, N. Rosenthal-Strauss, J. Dehnel, E. Lifshitz, S. Yochelis, R. D. Levine, F. Remacle, B. Fresch, G. Marcus, and Y. Paltiel, “Fast energy transfer in cdse quantum dot layered structures: controlling coupling with covalent-bond organic linkers,” J. Phys. Chem. C 122(10), 5753–5758 (2018).
[Crossref]

Panuganti, S.

S. Panuganti, L. V. Besteiro, E. S. Vasileiadou, J. M. Hoffman, A. O. Govorov, S. K. Gray, M. G. Kanatzidis, and R. D. Schaller, “Distance dependence of Förster resonance energy transfer rates in 2D perovskite quantum wells via control of organic spacer length,” J. Am. Chem. Soc. 143(11), 4244–4252 (2021).
[Crossref]

Parajó, M. F. G.

P. Ghenuche, M. Mivelle, J. de Torres, S. B. Moparthi, H. Rigneault, N. F. V. Hulst, M. F. G. Parajó, and J. Wenger, “Matching nanoantenna field confinement to FRET distances enhances Förster energy transfer rates,” Nano Lett. 15(9), 6193–6201 (2015).
[Crossref]

Park, Y. S.

Y. S. Park, J. Lim, N. S. Makarov, and V. I. Klimov, “Effect of interfacial alloying versus “volume scaling” on Auger recombination in compositionally graded semiconductor quantum dots,” Nano Lett. 17(9), 5607–5613 (2017).
[Crossref]

J. M. Pietryga, Y. S. Park, J. Lim, A. F. Fidler, W. K. Bae, S. Brovelli, and V. I. Klimov, “Spectroscopic and device aspects of nanocrystal quantum dots,” Chem. Rev. 116(18), 10513–10622 (2016).
[Crossref]

Y. S. Park, W. K. Bae, L. A. Padilha, J. M. Pietryga, and V. I. Klimov, “Effect of the core/shell interface on Auger recombination evaluated by single-quantum-dot spectroscopy,” Nano Lett. 14(2), 396–402 (2014).
[Crossref]

W. K. Bae, Y. S. Park, J. Lim, D. Lee, L. A. Padilha, H. McDaniel, I. Robel, C. Lee, J. M. Pietryga, and V. I. Klimov, “Controlling the influence of Auger recombination on the performance of quantum-dot light-emitting diodes,” Nat. Commun. 4(1), 2661 (2013).
[Crossref]

W. K. Bae, L. A. Padilha, Y. S. Park, H. McDaniel, I. Robel, J. M. Pietryga, and V. I. Klimov, “Controlled alloying of the core-shell interface in cdse/cds quantum dots for suppression of Auger recombination,” ACS Nano 7(4), 3411–3419 (2013).
[Crossref]

Peng, X.

X. Hou, J. Kang, H. Qin, X. Chen, J. Ma, J. Zhou, L. Chen, L. Wang, L-W. Wang, and X. Peng, “Engineering Auger recombination in colloidal quantum dots via dielectric screening,” Nat. Commun. 10(1), 1750 (2019).
[Crossref]

Pérez-Medina, C.

A. J. P. Teunissen, C. Pérez-Medina, A. Meijerink, and W. J. M. Mulder, “Investigating supramolecular systems using Förster resonance energy transfer,” Chem. Soc. Rev. 47(18), 7027–7044 (2018).
[Crossref]

Pi, X.

J. Gao, H. Zhang, X. Liu, N. Zhou, X. Pi, D. Li, and D. Yang, “Plasmon-coupled Förster resonance energy transfer between silicon quantim dots,” J. Phys. Chem. C 123(38), 23604–23609 (2019).
[Crossref]

Pietryga, J. M.

J. M. Pietryga, Y. S. Park, J. Lim, A. F. Fidler, W. K. Bae, S. Brovelli, and V. I. Klimov, “Spectroscopic and device aspects of nanocrystal quantum dots,” Chem. Rev. 116(18), 10513–10622 (2016).
[Crossref]

Y. S. Park, W. K. Bae, L. A. Padilha, J. M. Pietryga, and V. I. Klimov, “Effect of the core/shell interface on Auger recombination evaluated by single-quantum-dot spectroscopy,” Nano Lett. 14(2), 396–402 (2014).
[Crossref]

W. K. Bae, L. A. Padilha, Y. S. Park, H. McDaniel, I. Robel, J. M. Pietryga, and V. I. Klimov, “Controlled alloying of the core-shell interface in cdse/cds quantum dots for suppression of Auger recombination,” ACS Nano 7(4), 3411–3419 (2013).
[Crossref]

W. K. Bae, Y. S. Park, J. Lim, D. Lee, L. A. Padilha, H. McDaniel, I. Robel, C. Lee, J. M. Pietryga, and V. I. Klimov, “Controlling the influence of Auger recombination on the performance of quantum-dot light-emitting diodes,” Nat. Commun. 4(1), 2661 (2013).
[Crossref]

Pons, T.

S. Jana, X. Xu, A. Klymchenko, A. Reisch, and T. Pons, “Microcavity-enhanced fluorescence energy transfer from quantum dot excited whispering gallery modes to acceptor dye nanoparticles,” ACS Nano 15(1), 1445–1453 (2021).
[Crossref]

A. R. Clapp, T. Pons, I. L. Medintz, J. B. Delehanty, J. S. Melinger, T. Tiefenbrunn, P. E. Dawson, B. R. Fisher, B. O’Rourke, and H. Mattoussi, “Two-photon excitation of quantum-dot-based fluorescence resonance energy transfer and its applications,” Adv. Mater. 19(15), 1921–1926 (2007).
[Crossref]

Pramanik, S.

S. Pramanik, S. Bhandari, S. Roy, and A. Chattopadhyay, “Synchronous tricolor emission-based white light from quantum dot complex,” J. Phys. Chem. Lett. 6(7), 1270–1274 (2015).
[Crossref]

Pullerits, T.

B. Yang, J. S. Chen, S. Q. Yang, F. Hong, L. Sun, P. G. Han, T. Pullerits, W. Q. Deng, and K. L. Han, “Lead-free silver-bismuth halide double perovskite nanocrystals,” Angew. Chem. Int. Ed. 57(19), 5359–5363 (2018).
[Crossref]

Qin, C.

W. Guo, J. Tang, G. Zhang, B. Li, C. Yang, R. Chen, C. Qin, J. Hu, H. Zhong, L. Xiao, and S. Jia, “Photoluminescence blinking and biexcition Auger recombination in single colloidal quantum dots with sharp and smooth core/shell interfaces,” J. Phys. Chem. Lett. 12(1), 405–412 (2021).
[Crossref]

Qin, H.

X. Hou, J. Kang, H. Qin, X. Chen, J. Ma, J. Zhou, L. Chen, L. Wang, L-W. Wang, and X. Peng, “Engineering Auger recombination in colloidal quantum dots via dielectric screening,” Nat. Commun. 10(1), 1750 (2019).
[Crossref]

Raevskaya, A. E.

V. M. Dzhagan, M. Y. Valakh, A. E. Raevskaya, A. L. Stroyuk, S. Y. Kuchmiy, and D. R. T. Zahn, “Resonant raman scattering study of cdse nanocrystals passivated with cds and zns,” Nanotechnology 18(28), 285701 (2007).
[Crossref]

Ran, L. L.

Reisch, A.

S. Jana, X. Xu, A. Klymchenko, A. Reisch, and T. Pons, “Microcavity-enhanced fluorescence energy transfer from quantum dot excited whispering gallery modes to acceptor dye nanoparticles,” ACS Nano 15(1), 1445–1453 (2021).
[Crossref]

Remacle, F.

E. Cohen, P. Komm, N. Rosenthal-Strauss, J. Dehnel, E. Lifshitz, S. Yochelis, R. D. Levine, F. Remacle, B. Fresch, G. Marcus, and Y. Paltiel, “Fast energy transfer in cdse quantum dot layered structures: controlling coupling with covalent-bond organic linkers,” J. Phys. Chem. C 122(10), 5753–5758 (2018).
[Crossref]

Ren, S. Q.

S. Q. Ren, L. Y. Chang, S. K. Lim, J. Zhao, M. Smith, N. Zhao, V. Bulovic, M. Bawendi, and S. Gradecak, “Inorganic-organic hybrid solar cell: bridging quantum dots to conjugated polymer nanowires,” Nano Lett. 11(9), 3998–4002 (2011).
[Crossref]

Ren, T.

L. Dworak, V. V. Matylitsky, T. Ren, T. Basche, and J. Wachtveitl, “Acceptor concentration dependence of Förster resonance energy transfer dynamics in dye-quantum dot complexes,” J. Phys. Chem. C 118(8), 4396–4402 (2014).
[Crossref]

Resch-Genger, U.

V. Muhr, C. Wurth, M. Kraft, M. Buchner, A. J. Baeumner, U. Resch-Genger, and T. Hirsch, “Particle-size-dependent Förster resonance energy transfer from upconversion nanoparticles to organic dyes,” Anal. Chem. 89(9), 4868–4874 (2017).
[Crossref]

Rigneault, H.

P. Ghenuche, M. Mivelle, J. de Torres, S. B. Moparthi, H. Rigneault, N. F. V. Hulst, M. F. G. Parajó, and J. Wenger, “Matching nanoantenna field confinement to FRET distances enhances Förster energy transfer rates,” Nano Lett. 15(9), 6193–6201 (2015).
[Crossref]

Robel, I.

W. K. Bae, L. A. Padilha, Y. S. Park, H. McDaniel, I. Robel, J. M. Pietryga, and V. I. Klimov, “Controlled alloying of the core-shell interface in cdse/cds quantum dots for suppression of Auger recombination,” ACS Nano 7(4), 3411–3419 (2013).
[Crossref]

W. K. Bae, Y. S. Park, J. Lim, D. Lee, L. A. Padilha, H. McDaniel, I. Robel, C. Lee, J. M. Pietryga, and V. I. Klimov, “Controlling the influence of Auger recombination on the performance of quantum-dot light-emitting diodes,” Nat. Commun. 4(1), 2661 (2013).
[Crossref]

Rodina, A.

R. Vaxenburg, A. Rodina, A. Shabaev, E. Lifshitz, and A. L. Efros, “Nonradiative Auger recombination in semiconductor nanocrystals,” Nano Lett. 15(3), 2092–2098 (2015).
[Crossref]

Rogach, A. L.

T. Franzl, A. Shavel, A. L. Rogach, N. Gaponik, T. A. Klar, A. Eychmüller, and J. Feldmann, “High-rate unidirectional energy transfer in directly assembled cdte nanocrystal bilayers,” Small 1(4), 392–395 (2005).
[Crossref]

Rosenthal-Strauss, N.

E. Cohen, P. Komm, N. Rosenthal-Strauss, J. Dehnel, E. Lifshitz, S. Yochelis, R. D. Levine, F. Remacle, B. Fresch, G. Marcus, and Y. Paltiel, “Fast energy transfer in cdse quantum dot layered structures: controlling coupling with covalent-bond organic linkers,” J. Phys. Chem. C 122(10), 5753–5758 (2018).
[Crossref]

Rowland, C. E.

C. E. Rowland, I. Fedin, H. Zhang, S. K. Gray, A. O. Govorov, D. V. Talapin, and R. D. Schaller, “Picosecond energy transfer and multiexciton transfer outpaces Auger recombination in binary cdse nanoplatelet solids,” Nature Mater 14(5), 484–489 (2015).
[Crossref]

Roy, S.

S. Pramanik, S. Bhandari, S. Roy, and A. Chattopadhyay, “Synchronous tricolor emission-based white light from quantum dot complex,” J. Phys. Chem. Lett. 6(7), 1270–1274 (2015).
[Crossref]

Samarskaya, O.

Sapsford, K. E.

K. E. Sapsford, L. Berti, and I. L. Medintz, “Materials for fluorescence resonance energy transfer analysis: beyond traditional donor–acceptor combinations,” Angew. Chem. Int. Ed. 45(28), 4562–4589 (2006).
[Crossref]

Schaller, R. D.

S. Panuganti, L. V. Besteiro, E. S. Vasileiadou, J. M. Hoffman, A. O. Govorov, S. K. Gray, M. G. Kanatzidis, and R. D. Schaller, “Distance dependence of Förster resonance energy transfer rates in 2D perovskite quantum wells via control of organic spacer length,” J. Am. Chem. Soc. 143(11), 4244–4252 (2021).
[Crossref]

C. E. Rowland, I. Fedin, H. Zhang, S. K. Gray, A. O. Govorov, D. V. Talapin, and R. D. Schaller, “Picosecond energy transfer and multiexciton transfer outpaces Auger recombination in binary cdse nanoplatelet solids,” Nature Mater 14(5), 484–489 (2015).
[Crossref]

Sedgwick, A. C.

L. L. Wu, C. S. Huang, B. Emery, A. C. Sedgwick, S. D. Bull, X. P. He, H. Tian, J. Yoon, J. L. Sessler, and T. D. James, “Förster resonance energy transfer (FRET)-based small-molecule sensors and imaging agents,” Chem. Soc. Rev. 49(15), 5110–5139 (2020).
[Crossref]

Sessler, J. L.

L. L. Wu, C. S. Huang, B. Emery, A. C. Sedgwick, S. D. Bull, X. P. He, H. Tian, J. Yoon, J. L. Sessler, and T. D. James, “Förster resonance energy transfer (FRET)-based small-molecule sensors and imaging agents,” Chem. Soc. Rev. 49(15), 5110–5139 (2020).
[Crossref]

Shabaev, A.

R. Vaxenburg, A. Rodina, A. Shabaev, E. Lifshitz, and A. L. Efros, “Nonradiative Auger recombination in semiconductor nanocrystals,” Nano Lett. 15(3), 2092–2098 (2015).
[Crossref]

Shavel, A.

T. Franzl, A. Shavel, A. L. Rogach, N. Gaponik, T. A. Klar, A. Eychmüller, and J. Feldmann, “High-rate unidirectional energy transfer in directly assembled cdte nanocrystal bilayers,” Small 1(4), 392–395 (2005).
[Crossref]

Shi, S.

shi, Y.

H. Zong, X. Mu, J. Wang, H. Zhao, Y. shi, and M. Sun, “The nature of photoinduced intermolecular charge transfer in fluorescence resonance energy transfer,” Spectrochim. Acta, Part A 209(15), 228–233 (2019).
[Crossref]

X. Liu, J. Han, Y. Li, B. Cao, C. Sun, H. Yin, Y. Shi, M. Jin, C. Liu, M. Sun, and D. Ding, “Ultrafast carrier dynamics in all-inorganic CsPbBr3 perovskite across the pressure-induced phase transition,” Opt. Express 27(16), A995–1003 (2019).
[Crossref]

H.F. Zhao, H. Yin, X. C. Liu, H. Li, Y. Shi, C. L. Liu, M. X. Jin, J. B. Gao, Y. Luo, and D. J. Ding, “Pressure-induced tunable electron transfer and Auger recombination rates in cdse/zns quantum dot–anthraquinone complexes,” J. Phys. Chem. Lett. 10(11), 3064–3070 (2019).
[Crossref]

Smith, C.

C. Smith and D. Binks, “Multiple exciton generation in colloidal nanocrystals,” Nanomaterials 4(1), 19–45 (2014).
[Crossref]

Smith, M.

S. Q. Ren, L. Y. Chang, S. K. Lim, J. Zhao, M. Smith, N. Zhao, V. Bulovic, M. Bawendi, and S. Gradecak, “Inorganic-organic hybrid solar cell: bridging quantum dots to conjugated polymer nanowires,” Nano Lett. 11(9), 3998–4002 (2011).
[Crossref]

Song, N.

H. Zhu, N. Song, and T. Lian, “Controlling charge separation and recombination rates in cdse/zns type I core−shell quantum dots by shell thicknesses,” J. Am. Chem. Soc. 132(42), 15038–15045 (2010).
[Crossref]

Stroyuk, A. L.

V. M. Dzhagan, M. Y. Valakh, A. E. Raevskaya, A. L. Stroyuk, S. Y. Kuchmiy, and D. R. T. Zahn, “Resonant raman scattering study of cdse nanocrystals passivated with cds and zns,” Nanotechnology 18(28), 285701 (2007).
[Crossref]

Sun, B.

B.C. Huang, L. Xu, J. L. Zhu, Y. X. Wang, B. Sun, X. P. Li, and H. B. Yang, “Real-time monitoring the dynamics of coordination-driven self-assembly by fluorescence-resonance energy transfer,” J. Am. Chem. Soc. 139(28), 9459–9462 (2017).
[Crossref]

Sun, C.

Sun, L.

B. Yang, J. S. Chen, S. Q. Yang, F. Hong, L. Sun, P. G. Han, T. Pullerits, W. Q. Deng, and K. L. Han, “Lead-free silver-bismuth halide double perovskite nanocrystals,” Angew. Chem. Int. Ed. 57(19), 5359–5363 (2018).
[Crossref]

Sun, M.

X. Liu, J. Han, Y. Li, B. Cao, C. Sun, H. Yin, Y. Shi, M. Jin, C. Liu, M. Sun, and D. Ding, “Ultrafast carrier dynamics in all-inorganic CsPbBr3 perovskite across the pressure-induced phase transition,” Opt. Express 27(16), A995–1003 (2019).
[Crossref]

H. Zong, X. Mu, J. Wang, H. Zhao, Y. shi, and M. Sun, “The nature of photoinduced intermolecular charge transfer in fluorescence resonance energy transfer,” Spectrochim. Acta, Part A 209(15), 228–233 (2019).
[Crossref]

H. Zong, J. Wang, X. Mu, X. Xu, J. Li, X. Wang, F. Long, J. Wang, and M. Sun, “Physical mechanism of photoinduced intermolecular charge transfer enhanced by fluorescence resonance energy transfer,” Phys. Chem. Chem. Phys. 20(19), 13558–13565 (2018).
[Crossref]

Talapin, D. V.

C. E. Rowland, I. Fedin, H. Zhang, S. K. Gray, A. O. Govorov, D. V. Talapin, and R. D. Schaller, “Picosecond energy transfer and multiexciton transfer outpaces Auger recombination in binary cdse nanoplatelet solids,” Nature Mater 14(5), 484–489 (2015).
[Crossref]

Tang, J.

W. Guo, J. Tang, G. Zhang, B. Li, C. Yang, R. Chen, C. Qin, J. Hu, H. Zhong, L. Xiao, and S. Jia, “Photoluminescence blinking and biexcition Auger recombination in single colloidal quantum dots with sharp and smooth core/shell interfaces,” J. Phys. Chem. Lett. 12(1), 405–412 (2021).
[Crossref]

Teunissen, A. J. P.

A. J. P. Teunissen, C. Pérez-Medina, A. Meijerink, and W. J. M. Mulder, “Investigating supramolecular systems using Förster resonance energy transfer,” Chem. Soc. Rev. 47(18), 7027–7044 (2018).
[Crossref]

Tian, H.

L. L. Wu, C. S. Huang, B. Emery, A. C. Sedgwick, S. D. Bull, X. P. He, H. Tian, J. Yoon, J. L. Sessler, and T. D. James, “Förster resonance energy transfer (FRET)-based small-molecule sensors and imaging agents,” Chem. Soc. Rev. 49(15), 5110–5139 (2020).
[Crossref]

Tiefenbrunn, T.

A. R. Clapp, T. Pons, I. L. Medintz, J. B. Delehanty, J. S. Melinger, T. Tiefenbrunn, P. E. Dawson, B. R. Fisher, B. O’Rourke, and H. Mattoussi, “Two-photon excitation of quantum-dot-based fluorescence resonance energy transfer and its applications,” Adv. Mater. 19(15), 1921–1926 (2007).
[Crossref]

Valakh, M. Y.

V. M. Dzhagan, M. Y. Valakh, A. E. Raevskaya, A. L. Stroyuk, S. Y. Kuchmiy, and D. R. T. Zahn, “Resonant raman scattering study of cdse nanocrystals passivated with cds and zns,” Nanotechnology 18(28), 285701 (2007).
[Crossref]

Vasileiadou, E. S.

S. Panuganti, L. V. Besteiro, E. S. Vasileiadou, J. M. Hoffman, A. O. Govorov, S. K. Gray, M. G. Kanatzidis, and R. D. Schaller, “Distance dependence of Förster resonance energy transfer rates in 2D perovskite quantum wells via control of organic spacer length,” J. Am. Chem. Soc. 143(11), 4244–4252 (2021).
[Crossref]

Vaxenburg, R.

R. Vaxenburg, A. Rodina, A. Shabaev, E. Lifshitz, and A. L. Efros, “Nonradiative Auger recombination in semiconductor nanocrystals,” Nano Lett. 15(3), 2092–2098 (2015).
[Crossref]

Viswanatha, R.

F. Garcia-Santamaria, S. Brovelli, R. Viswanatha, J. A. Hollingsworth, H. Htoon, S. A. Crooker, and V. I. Klimov, “Breakdown of volume scaling in Auger recombination in cdse/cds heteronanocrystals: the role of the core-shell interface,” Nano Lett. 11(2), 687–693 (2011).
[Crossref]

Voorhees, P. W.

J. E. Guyer and P. W. Voorhees, “Morphological stability of alloy thin films,” Phys. Rev. Lett. 74(20), 4031–4034 (1995).
[Crossref]

Wachtveitl, J.

L. Dworak, V. V. Matylitsky, T. Ren, T. Basche, and J. Wachtveitl, “Acceptor concentration dependence of Förster resonance energy transfer dynamics in dye-quantum dot complexes,” J. Phys. Chem. C 118(8), 4396–4402 (2014).
[Crossref]

Wang, J.

H. Zong, X. Mu, J. Wang, H. Zhao, Y. shi, and M. Sun, “The nature of photoinduced intermolecular charge transfer in fluorescence resonance energy transfer,” Spectrochim. Acta, Part A 209(15), 228–233 (2019).
[Crossref]

H. Zong, J. Wang, X. Mu, X. Xu, J. Li, X. Wang, F. Long, J. Wang, and M. Sun, “Physical mechanism of photoinduced intermolecular charge transfer enhanced by fluorescence resonance energy transfer,” Phys. Chem. Chem. Phys. 20(19), 13558–13565 (2018).
[Crossref]

H. Zong, J. Wang, X. Mu, X. Xu, J. Li, X. Wang, F. Long, J. Wang, and M. Sun, “Physical mechanism of photoinduced intermolecular charge transfer enhanced by fluorescence resonance energy transfer,” Phys. Chem. Chem. Phys. 20(19), 13558–13565 (2018).
[Crossref]

Wang, L.

X. Hou, J. Kang, H. Qin, X. Chen, J. Ma, J. Zhou, L. Chen, L. Wang, L-W. Wang, and X. Peng, “Engineering Auger recombination in colloidal quantum dots via dielectric screening,” Nat. Commun. 10(1), 1750 (2019).
[Crossref]

Wang, L-W.

X. Hou, J. Kang, H. Qin, X. Chen, J. Ma, J. Zhou, L. Chen, L. Wang, L-W. Wang, and X. Peng, “Engineering Auger recombination in colloidal quantum dots via dielectric screening,” Nat. Commun. 10(1), 1750 (2019).
[Crossref]

Wang, X.

H. Zong, J. Wang, X. Mu, X. Xu, J. Li, X. Wang, F. Long, J. Wang, and M. Sun, “Physical mechanism of photoinduced intermolecular charge transfer enhanced by fluorescence resonance energy transfer,” Phys. Chem. Chem. Phys. 20(19), 13558–13565 (2018).
[Crossref]

Wang, Y. X.

B.C. Huang, L. Xu, J. L. Zhu, Y. X. Wang, B. Sun, X. P. Li, and H. B. Yang, “Real-time monitoring the dynamics of coordination-driven self-assembly by fluorescence-resonance energy transfer,” J. Am. Chem. Soc. 139(28), 9459–9462 (2017).
[Crossref]

Wang, Z.

F. Bai, K. Bian, X. Huang, Z. Wang, and H. Fan, “Pressure induced nanoparticle phase behavior, property, and applications,” Chem. Rev. 119(12), 7673–7717 (2019).
[Crossref]

Weaver, M. J.

S. Zou and M. J. Weaver, “Surface-enhanced raman spectroscopy of cadmium sulfide/cadmium selenide superlattices formed on gold by electrochemical atomic-layer epitaxy,” Chem. Phys. Lett. 312(2-4), 101–107 (1999).
[Crossref]

Weiss, E. A.

A. J. Morris-Cohen, M. T. Frederick, L. C. Cass, and E. A. Weiss, “Simultaneous determination of the adsorption constant and the photoinduced electron transfer rate for a cds quantum dot-violagen complex,” J. Am. Chem. Soc. 133(26), 10146–10154 (2011).
[Crossref]

Weiss, S.

E. Lerner, T. Cordes, A. Ingargiola, Y. Alhadid, S. Y. Chung, X. Michalet, and S. Weiss, “Toward dynamic structural biology: two decades of singer-molexule Förster resonance energy transfer,” Science359(6373), eaan1133 (2018).
[Crossref]

Wenger, J.

P. Ghenuche, M. Mivelle, J. de Torres, S. B. Moparthi, H. Rigneault, N. F. V. Hulst, M. F. G. Parajó, and J. Wenger, “Matching nanoantenna field confinement to FRET distances enhances Förster energy transfer rates,” Nano Lett. 15(9), 6193–6201 (2015).
[Crossref]

Wu, C.

W. Bi, X. Li, L. Zhang, T. Jin, L. Zhang, Q. Zhang, Y. Luo, C. Wu, and Y. Xie, “Molecular co-catalyst accelerating hole transfer for enhanced photocatalytic H2 evolution,” Nat. Commun. 6(1), 8647 (2015).
[Crossref]

Wu, K. F.

Y. L. Li and K. F. Wu, “Size and halide dependent Auger recombination in lead halide perovskite nanocrystals,” Angew. Chem. Int. Edit. 59(34), 14292–14295 (2020).
[Crossref]

Wu, L. L.

L. L. Wu, C. S. Huang, B. Emery, A. C. Sedgwick, S. D. Bull, X. P. He, H. Tian, J. Yoon, J. L. Sessler, and T. D. James, “Förster resonance energy transfer (FRET)-based small-molecule sensors and imaging agents,” Chem. Soc. Rev. 49(15), 5110–5139 (2020).
[Crossref]

Wu, W. Z.

Wurth, C.

V. Muhr, C. Wurth, M. Kraft, M. Buchner, A. J. Baeumner, U. Resch-Genger, and T. Hirsch, “Particle-size-dependent Förster resonance energy transfer from upconversion nanoparticles to organic dyes,” Anal. Chem. 89(9), 4868–4874 (2017).
[Crossref]

Xiao, J.

Xiao, L.

W. Guo, J. Tang, G. Zhang, B. Li, C. Yang, R. Chen, C. Qin, J. Hu, H. Zhong, L. Xiao, and S. Jia, “Photoluminescence blinking and biexcition Auger recombination in single colloidal quantum dots with sharp and smooth core/shell interfaces,” J. Phys. Chem. Lett. 12(1), 405–412 (2021).
[Crossref]

Xie, Y.

W. Bi, X. Li, L. Zhang, T. Jin, L. Zhang, Q. Zhang, Y. Luo, C. Wu, and Y. Xie, “Molecular co-catalyst accelerating hole transfer for enhanced photocatalytic H2 evolution,” Nat. Commun. 6(1), 8647 (2015).
[Crossref]

Xu, L.

B.C. Huang, L. Xu, J. L. Zhu, Y. X. Wang, B. Sun, X. P. Li, and H. B. Yang, “Real-time monitoring the dynamics of coordination-driven self-assembly by fluorescence-resonance energy transfer,” J. Am. Chem. Soc. 139(28), 9459–9462 (2017).
[Crossref]

Xu, X.

S. Jana, X. Xu, A. Klymchenko, A. Reisch, and T. Pons, “Microcavity-enhanced fluorescence energy transfer from quantum dot excited whispering gallery modes to acceptor dye nanoparticles,” ACS Nano 15(1), 1445–1453 (2021).
[Crossref]

H. Zong, J. Wang, X. Mu, X. Xu, J. Li, X. Wang, F. Long, J. Wang, and M. Sun, “Physical mechanism of photoinduced intermolecular charge transfer enhanced by fluorescence resonance energy transfer,” Phys. Chem. Chem. Phys. 20(19), 13558–13565 (2018).
[Crossref]

Yang, B.

B. Yang, J. S. Chen, S. Q. Yang, F. Hong, L. Sun, P. G. Han, T. Pullerits, W. Q. Deng, and K. L. Han, “Lead-free silver-bismuth halide double perovskite nanocrystals,” Angew. Chem. Int. Ed. 57(19), 5359–5363 (2018).
[Crossref]

Yang, C.

W. Guo, J. Tang, G. Zhang, B. Li, C. Yang, R. Chen, C. Qin, J. Hu, H. Zhong, L. Xiao, and S. Jia, “Photoluminescence blinking and biexcition Auger recombination in single colloidal quantum dots with sharp and smooth core/shell interfaces,” J. Phys. Chem. Lett. 12(1), 405–412 (2021).
[Crossref]

Yang, D.

J. Gao, H. Zhang, X. Liu, N. Zhou, X. Pi, D. Li, and D. Yang, “Plasmon-coupled Förster resonance energy transfer between silicon quantim dots,” J. Phys. Chem. C 123(38), 23604–23609 (2019).
[Crossref]

Yang, G.

Yang, H. B.

B.C. Huang, L. Xu, J. L. Zhu, Y. X. Wang, B. Sun, X. P. Li, and H. B. Yang, “Real-time monitoring the dynamics of coordination-driven self-assembly by fluorescence-resonance energy transfer,” J. Am. Chem. Soc. 139(28), 9459–9462 (2017).
[Crossref]

Yang, S. Q.

B. Yang, J. S. Chen, S. Q. Yang, F. Hong, L. Sun, P. G. Han, T. Pullerits, W. Q. Deng, and K. L. Han, “Lead-free silver-bismuth halide double perovskite nanocrystals,” Angew. Chem. Int. Ed. 57(19), 5359–5363 (2018).
[Crossref]

Yazeva, T. V.

D. I. Chepic, Al. L. Efros, A. I. Ekimov, M. G. Ivanov, V. A. Kharchenko, I. A. Kudriavtsev, and T. V. Yazeva, “Auger ionization of semiconductor quantum drops in a glass matrix,” J. Lumin. 47(3), 113–127 (1990).
[Crossref]

Yin, H.

X. Liu, J. Han, Y. Li, B. Cao, C. Sun, H. Yin, Y. Shi, M. Jin, C. Liu, M. Sun, and D. Ding, “Ultrafast carrier dynamics in all-inorganic CsPbBr3 perovskite across the pressure-induced phase transition,” Opt. Express 27(16), A995–1003 (2019).
[Crossref]

H.F. Zhao, H. Yin, X. C. Liu, H. Li, Y. Shi, C. L. Liu, M. X. Jin, J. B. Gao, Y. Luo, and D. J. Ding, “Pressure-induced tunable electron transfer and Auger recombination rates in cdse/zns quantum dot–anthraquinone complexes,” J. Phys. Chem. Lett. 10(11), 3064–3070 (2019).
[Crossref]

Yochelis, S.

E. Cohen, P. Komm, N. Rosenthal-Strauss, J. Dehnel, E. Lifshitz, S. Yochelis, R. D. Levine, F. Remacle, B. Fresch, G. Marcus, and Y. Paltiel, “Fast energy transfer in cdse quantum dot layered structures: controlling coupling with covalent-bond organic linkers,” J. Phys. Chem. C 122(10), 5753–5758 (2018).
[Crossref]

Yoon, J.

L. L. Wu, C. S. Huang, B. Emery, A. C. Sedgwick, S. D. Bull, X. P. He, H. Tian, J. Yoon, J. L. Sessler, and T. D. James, “Förster resonance energy transfer (FRET)-based small-molecule sensors and imaging agents,” Chem. Soc. Rev. 49(15), 5110–5139 (2020).
[Crossref]

Zahn, D. R. T.

V. M. Dzhagan, M. Y. Valakh, A. E. Raevskaya, A. L. Stroyuk, S. Y. Kuchmiy, and D. R. T. Zahn, “Resonant raman scattering study of cdse nanocrystals passivated with cds and zns,” Nanotechnology 18(28), 285701 (2007).
[Crossref]

Zhang, G.

W. Guo, J. Tang, G. Zhang, B. Li, C. Yang, R. Chen, C. Qin, J. Hu, H. Zhong, L. Xiao, and S. Jia, “Photoluminescence blinking and biexcition Auger recombination in single colloidal quantum dots with sharp and smooth core/shell interfaces,” J. Phys. Chem. Lett. 12(1), 405–412 (2021).
[Crossref]

Zhang, H.

J. Gao, H. Zhang, X. Liu, N. Zhou, X. Pi, D. Li, and D. Yang, “Plasmon-coupled Förster resonance energy transfer between silicon quantim dots,” J. Phys. Chem. C 123(38), 23604–23609 (2019).
[Crossref]

C. E. Rowland, I. Fedin, H. Zhang, S. K. Gray, A. O. Govorov, D. V. Talapin, and R. D. Schaller, “Picosecond energy transfer and multiexciton transfer outpaces Auger recombination in binary cdse nanoplatelet solids,” Nature Mater 14(5), 484–489 (2015).
[Crossref]

Zhang, L.

W. Bi, X. Li, L. Zhang, T. Jin, L. Zhang, Q. Zhang, Y. Luo, C. Wu, and Y. Xie, “Molecular co-catalyst accelerating hole transfer for enhanced photocatalytic H2 evolution,” Nat. Commun. 6(1), 8647 (2015).
[Crossref]

W. Bi, X. Li, L. Zhang, T. Jin, L. Zhang, Q. Zhang, Y. Luo, C. Wu, and Y. Xie, “Molecular co-catalyst accelerating hole transfer for enhanced photocatalytic H2 evolution,” Nat. Commun. 6(1), 8647 (2015).
[Crossref]

Zhang, Q.

W. Bi, X. Li, L. Zhang, T. Jin, L. Zhang, Q. Zhang, Y. Luo, C. Wu, and Y. Xie, “Molecular co-catalyst accelerating hole transfer for enhanced photocatalytic H2 evolution,” Nat. Commun. 6(1), 8647 (2015).
[Crossref]

Zhang, W.

Zhang, X.

Zhao, H.

H. Zong, X. Mu, J. Wang, H. Zhao, Y. shi, and M. Sun, “The nature of photoinduced intermolecular charge transfer in fluorescence resonance energy transfer,” Spectrochim. Acta, Part A 209(15), 228–233 (2019).
[Crossref]

Zhao, H.F.

H.F. Zhao, H. Yin, X. C. Liu, H. Li, Y. Shi, C. L. Liu, M. X. Jin, J. B. Gao, Y. Luo, and D. J. Ding, “Pressure-induced tunable electron transfer and Auger recombination rates in cdse/zns quantum dot–anthraquinone complexes,” J. Phys. Chem. Lett. 10(11), 3064–3070 (2019).
[Crossref]

Zhao, J.

S. Q. Ren, L. Y. Chang, S. K. Lim, J. Zhao, M. Smith, N. Zhao, V. Bulovic, M. Bawendi, and S. Gradecak, “Inorganic-organic hybrid solar cell: bridging quantum dots to conjugated polymer nanowires,” Nano Lett. 11(9), 3998–4002 (2011).
[Crossref]

Zhao, N.

S. Q. Ren, L. Y. Chang, S. K. Lim, J. Zhao, M. Smith, N. Zhao, V. Bulovic, M. Bawendi, and S. Gradecak, “Inorganic-organic hybrid solar cell: bridging quantum dots to conjugated polymer nanowires,” Nano Lett. 11(9), 3998–4002 (2011).
[Crossref]

Zhong, H.

W. Guo, J. Tang, G. Zhang, B. Li, C. Yang, R. Chen, C. Qin, J. Hu, H. Zhong, L. Xiao, and S. Jia, “Photoluminescence blinking and biexcition Auger recombination in single colloidal quantum dots with sharp and smooth core/shell interfaces,” J. Phys. Chem. Lett. 12(1), 405–412 (2021).
[Crossref]

Zhou, J.

X. Hou, J. Kang, H. Qin, X. Chen, J. Ma, J. Zhou, L. Chen, L. Wang, L-W. Wang, and X. Peng, “Engineering Auger recombination in colloidal quantum dots via dielectric screening,” Nat. Commun. 10(1), 1750 (2019).
[Crossref]

Zhou, N.

J. Gao, H. Zhang, X. Liu, N. Zhou, X. Pi, D. Li, and D. Yang, “Plasmon-coupled Förster resonance energy transfer between silicon quantim dots,” J. Phys. Chem. C 123(38), 23604–23609 (2019).
[Crossref]

Zhou, S.

Zhu, H.

H. Zhu, N. Song, and T. Lian, “Controlling charge separation and recombination rates in cdse/zns type I core−shell quantum dots by shell thicknesses,” J. Am. Chem. Soc. 132(42), 15038–15045 (2010).
[Crossref]

Zhu, J. L.

B.C. Huang, L. Xu, J. L. Zhu, Y. X. Wang, B. Sun, X. P. Li, and H. B. Yang, “Real-time monitoring the dynamics of coordination-driven self-assembly by fluorescence-resonance energy transfer,” J. Am. Chem. Soc. 139(28), 9459–9462 (2017).
[Crossref]

Zong, H.

H. Zong, X. Mu, J. Wang, H. Zhao, Y. shi, and M. Sun, “The nature of photoinduced intermolecular charge transfer in fluorescence resonance energy transfer,” Spectrochim. Acta, Part A 209(15), 228–233 (2019).
[Crossref]

H. Zong, J. Wang, X. Mu, X. Xu, J. Li, X. Wang, F. Long, J. Wang, and M. Sun, “Physical mechanism of photoinduced intermolecular charge transfer enhanced by fluorescence resonance energy transfer,” Phys. Chem. Chem. Phys. 20(19), 13558–13565 (2018).
[Crossref]

Zou, S.

S. Zou and M. J. Weaver, “Surface-enhanced raman spectroscopy of cadmium sulfide/cadmium selenide superlattices formed on gold by electrochemical atomic-layer epitaxy,” Chem. Phys. Lett. 312(2-4), 101–107 (1999).
[Crossref]

ACS Nano (2)

S. Jana, X. Xu, A. Klymchenko, A. Reisch, and T. Pons, “Microcavity-enhanced fluorescence energy transfer from quantum dot excited whispering gallery modes to acceptor dye nanoparticles,” ACS Nano 15(1), 1445–1453 (2021).
[Crossref]

W. K. Bae, L. A. Padilha, Y. S. Park, H. McDaniel, I. Robel, J. M. Pietryga, and V. I. Klimov, “Controlled alloying of the core-shell interface in cdse/cds quantum dots for suppression of Auger recombination,” ACS Nano 7(4), 3411–3419 (2013).
[Crossref]

ACS Photonics (1)

J. Gao, S. C. Nguyen, N. D. Bronstein, and A. P. Alivisatos, “Solution-processed, high-speed, and high-quantum-efficiency quantum dot infrared photodetectors,” ACS Photonics 3(7), 1217–1222 (2016).
[Crossref]

Adv. Mater. (1)

A. R. Clapp, T. Pons, I. L. Medintz, J. B. Delehanty, J. S. Melinger, T. Tiefenbrunn, P. E. Dawson, B. R. Fisher, B. O’Rourke, and H. Mattoussi, “Two-photon excitation of quantum-dot-based fluorescence resonance energy transfer and its applications,” Adv. Mater. 19(15), 1921–1926 (2007).
[Crossref]

Anal. Chem. (1)

V. Muhr, C. Wurth, M. Kraft, M. Buchner, A. J. Baeumner, U. Resch-Genger, and T. Hirsch, “Particle-size-dependent Förster resonance energy transfer from upconversion nanoparticles to organic dyes,” Anal. Chem. 89(9), 4868–4874 (2017).
[Crossref]

Angew. Chem. Int. Ed. (2)

K. E. Sapsford, L. Berti, and I. L. Medintz, “Materials for fluorescence resonance energy transfer analysis: beyond traditional donor–acceptor combinations,” Angew. Chem. Int. Ed. 45(28), 4562–4589 (2006).
[Crossref]

B. Yang, J. S. Chen, S. Q. Yang, F. Hong, L. Sun, P. G. Han, T. Pullerits, W. Q. Deng, and K. L. Han, “Lead-free silver-bismuth halide double perovskite nanocrystals,” Angew. Chem. Int. Ed. 57(19), 5359–5363 (2018).
[Crossref]

Angew. Chem. Int. Edit. (1)

Y. L. Li and K. F. Wu, “Size and halide dependent Auger recombination in lead halide perovskite nanocrystals,” Angew. Chem. Int. Edit. 59(34), 14292–14295 (2020).
[Crossref]

Annu. Rev. Condens. Matter Phys. (1)

V. I. Klimov, “Multicarrier interactions in semiconductor nanocrystals in relation to the phenomena of Auger recombination and carrier multiplication,” Annu. Rev. Condens. Matter Phys. 5(1), 285–316 (2014).
[Crossref]

Chem. Phys. Lett. (1)

S. Zou and M. J. Weaver, “Surface-enhanced raman spectroscopy of cadmium sulfide/cadmium selenide superlattices formed on gold by electrochemical atomic-layer epitaxy,” Chem. Phys. Lett. 312(2-4), 101–107 (1999).
[Crossref]

Chem. Rev. (2)

F. Bai, K. Bian, X. Huang, Z. Wang, and H. Fan, “Pressure induced nanoparticle phase behavior, property, and applications,” Chem. Rev. 119(12), 7673–7717 (2019).
[Crossref]

J. M. Pietryga, Y. S. Park, J. Lim, A. F. Fidler, W. K. Bae, S. Brovelli, and V. I. Klimov, “Spectroscopic and device aspects of nanocrystal quantum dots,” Chem. Rev. 116(18), 10513–10622 (2016).
[Crossref]

Chem. Soc. Rev. (2)

A. J. P. Teunissen, C. Pérez-Medina, A. Meijerink, and W. J. M. Mulder, “Investigating supramolecular systems using Förster resonance energy transfer,” Chem. Soc. Rev. 47(18), 7027–7044 (2018).
[Crossref]

L. L. Wu, C. S. Huang, B. Emery, A. C. Sedgwick, S. D. Bull, X. P. He, H. Tian, J. Yoon, J. L. Sessler, and T. D. James, “Förster resonance energy transfer (FRET)-based small-molecule sensors and imaging agents,” Chem. Soc. Rev. 49(15), 5110–5139 (2020).
[Crossref]

J. Am. Chem. Soc. (5)

S. Panuganti, L. V. Besteiro, E. S. Vasileiadou, J. M. Hoffman, A. O. Govorov, S. K. Gray, M. G. Kanatzidis, and R. D. Schaller, “Distance dependence of Förster resonance energy transfer rates in 2D perovskite quantum wells via control of organic spacer length,” J. Am. Chem. Soc. 143(11), 4244–4252 (2021).
[Crossref]

B.C. Huang, L. Xu, J. L. Zhu, Y. X. Wang, B. Sun, X. P. Li, and H. B. Yang, “Real-time monitoring the dynamics of coordination-driven self-assembly by fluorescence-resonance energy transfer,” J. Am. Chem. Soc. 139(28), 9459–9462 (2017).
[Crossref]

A. R. Clapp, I. L. Medintz, J. M. Mauro, B. R. Fisher, M. G. Bawendi, and H. Mattoussi, “Fluorescence resonance energy transfer between quantum dot donors and dye-labeled protein acceptors,” J. Am. Chem. Soc. 126(1), 301–310 (2004).
[Crossref]

A. J. Morris-Cohen, M. T. Frederick, L. C. Cass, and E. A. Weiss, “Simultaneous determination of the adsorption constant and the photoinduced electron transfer rate for a cds quantum dot-violagen complex,” J. Am. Chem. Soc. 133(26), 10146–10154 (2011).
[Crossref]

H. Zhu, N. Song, and T. Lian, “Controlling charge separation and recombination rates in cdse/zns type I core−shell quantum dots by shell thicknesses,” J. Am. Chem. Soc. 132(42), 15038–15045 (2010).
[Crossref]

J. Lumin. (1)

D. I. Chepic, Al. L. Efros, A. I. Ekimov, M. G. Ivanov, V. A. Kharchenko, I. A. Kudriavtsev, and T. V. Yazeva, “Auger ionization of semiconductor quantum drops in a glass matrix,” J. Lumin. 47(3), 113–127 (1990).
[Crossref]

J. Phys. Chem. C (3)

J. Gao, H. Zhang, X. Liu, N. Zhou, X. Pi, D. Li, and D. Yang, “Plasmon-coupled Förster resonance energy transfer between silicon quantim dots,” J. Phys. Chem. C 123(38), 23604–23609 (2019).
[Crossref]

L. Dworak, V. V. Matylitsky, T. Ren, T. Basche, and J. Wachtveitl, “Acceptor concentration dependence of Förster resonance energy transfer dynamics in dye-quantum dot complexes,” J. Phys. Chem. C 118(8), 4396–4402 (2014).
[Crossref]

E. Cohen, P. Komm, N. Rosenthal-Strauss, J. Dehnel, E. Lifshitz, S. Yochelis, R. D. Levine, F. Remacle, B. Fresch, G. Marcus, and Y. Paltiel, “Fast energy transfer in cdse quantum dot layered structures: controlling coupling with covalent-bond organic linkers,” J. Phys. Chem. C 122(10), 5753–5758 (2018).
[Crossref]

J. Phys. Chem. Lett. (3)

W. Guo, J. Tang, G. Zhang, B. Li, C. Yang, R. Chen, C. Qin, J. Hu, H. Zhong, L. Xiao, and S. Jia, “Photoluminescence blinking and biexcition Auger recombination in single colloidal quantum dots with sharp and smooth core/shell interfaces,” J. Phys. Chem. Lett. 12(1), 405–412 (2021).
[Crossref]

H.F. Zhao, H. Yin, X. C. Liu, H. Li, Y. Shi, C. L. Liu, M. X. Jin, J. B. Gao, Y. Luo, and D. J. Ding, “Pressure-induced tunable electron transfer and Auger recombination rates in cdse/zns quantum dot–anthraquinone complexes,” J. Phys. Chem. Lett. 10(11), 3064–3070 (2019).
[Crossref]

S. Pramanik, S. Bhandari, S. Roy, and A. Chattopadhyay, “Synchronous tricolor emission-based white light from quantum dot complex,” J. Phys. Chem. Lett. 6(7), 1270–1274 (2015).
[Crossref]

Nano Lett. (7)

G. E. Cragg and A. L. Efros, “Suppression of Auger processes in confined structures,” Nano Lett. 10(1), 313–317 (2010).
[Crossref]

Y. S. Park, J. Lim, N. S. Makarov, and V. I. Klimov, “Effect of interfacial alloying versus “volume scaling” on Auger recombination in compositionally graded semiconductor quantum dots,” Nano Lett. 17(9), 5607–5613 (2017).
[Crossref]

Y. S. Park, W. K. Bae, L. A. Padilha, J. M. Pietryga, and V. I. Klimov, “Effect of the core/shell interface on Auger recombination evaluated by single-quantum-dot spectroscopy,” Nano Lett. 14(2), 396–402 (2014).
[Crossref]

F. Garcia-Santamaria, S. Brovelli, R. Viswanatha, J. A. Hollingsworth, H. Htoon, S. A. Crooker, and V. I. Klimov, “Breakdown of volume scaling in Auger recombination in cdse/cds heteronanocrystals: the role of the core-shell interface,” Nano Lett. 11(2), 687–693 (2011).
[Crossref]

R. Vaxenburg, A. Rodina, A. Shabaev, E. Lifshitz, and A. L. Efros, “Nonradiative Auger recombination in semiconductor nanocrystals,” Nano Lett. 15(3), 2092–2098 (2015).
[Crossref]

S. Q. Ren, L. Y. Chang, S. K. Lim, J. Zhao, M. Smith, N. Zhao, V. Bulovic, M. Bawendi, and S. Gradecak, “Inorganic-organic hybrid solar cell: bridging quantum dots to conjugated polymer nanowires,” Nano Lett. 11(9), 3998–4002 (2011).
[Crossref]

P. Ghenuche, M. Mivelle, J. de Torres, S. B. Moparthi, H. Rigneault, N. F. V. Hulst, M. F. G. Parajó, and J. Wenger, “Matching nanoantenna field confinement to FRET distances enhances Förster energy transfer rates,” Nano Lett. 15(9), 6193–6201 (2015).
[Crossref]

Nanomaterials (1)

C. Smith and D. Binks, “Multiple exciton generation in colloidal nanocrystals,” Nanomaterials 4(1), 19–45 (2014).
[Crossref]

Nanotechnology (1)

V. M. Dzhagan, M. Y. Valakh, A. E. Raevskaya, A. L. Stroyuk, S. Y. Kuchmiy, and D. R. T. Zahn, “Resonant raman scattering study of cdse nanocrystals passivated with cds and zns,” Nanotechnology 18(28), 285701 (2007).
[Crossref]

Nat. Commun. (3)

W. K. Bae, Y. S. Park, J. Lim, D. Lee, L. A. Padilha, H. McDaniel, I. Robel, C. Lee, J. M. Pietryga, and V. I. Klimov, “Controlling the influence of Auger recombination on the performance of quantum-dot light-emitting diodes,” Nat. Commun. 4(1), 2661 (2013).
[Crossref]

W. Bi, X. Li, L. Zhang, T. Jin, L. Zhang, Q. Zhang, Y. Luo, C. Wu, and Y. Xie, “Molecular co-catalyst accelerating hole transfer for enhanced photocatalytic H2 evolution,” Nat. Commun. 6(1), 8647 (2015).
[Crossref]

X. Hou, J. Kang, H. Qin, X. Chen, J. Ma, J. Zhou, L. Chen, L. Wang, L-W. Wang, and X. Peng, “Engineering Auger recombination in colloidal quantum dots via dielectric screening,” Nat. Commun. 10(1), 1750 (2019).
[Crossref]

Nature Mater (1)

C. E. Rowland, I. Fedin, H. Zhang, S. K. Gray, A. O. Govorov, D. V. Talapin, and R. D. Schaller, “Picosecond energy transfer and multiexciton transfer outpaces Auger recombination in binary cdse nanoplatelet solids,” Nature Mater 14(5), 484–489 (2015).
[Crossref]

Opt. Express (5)

Phys. Chem. Chem. Phys. (1)

H. Zong, J. Wang, X. Mu, X. Xu, J. Li, X. Wang, F. Long, J. Wang, and M. Sun, “Physical mechanism of photoinduced intermolecular charge transfer enhanced by fluorescence resonance energy transfer,” Phys. Chem. Chem. Phys. 20(19), 13558–13565 (2018).
[Crossref]

Phys. Rev. Lett. (1)

J. E. Guyer and P. W. Voorhees, “Morphological stability of alloy thin films,” Phys. Rev. Lett. 74(20), 4031–4034 (1995).
[Crossref]

Science (1)

V. I. Klimov, A. A. Mikhailovsky, D. W. Mcbranch, C. A. Leatherdale, and M. G. Bawendi, “Quantization of multiparticle Auger rates in semiconductor quantum dots,” Science 287(5455), 1011–1013 (2000).
[Crossref]

Small (1)

T. Franzl, A. Shavel, A. L. Rogach, N. Gaponik, T. A. Klar, A. Eychmüller, and J. Feldmann, “High-rate unidirectional energy transfer in directly assembled cdte nanocrystal bilayers,” Small 1(4), 392–395 (2005).
[Crossref]

Spectrochim. Acta, Part A (1)

H. Zong, X. Mu, J. Wang, H. Zhao, Y. shi, and M. Sun, “The nature of photoinduced intermolecular charge transfer in fluorescence resonance energy transfer,” Spectrochim. Acta, Part A 209(15), 228–233 (2019).
[Crossref]

Trends Anal. Chem. (1)

M. Cardoso Dos Santos, W. R. Algar, I. L. Medintz, and N. Hildebrandt, “Quantum dots for Förster resonance energy transfer (FRET),” Trends Anal. Chem. 125, 115819 (2020).
[Crossref]

Other (1)

E. Lerner, T. Cordes, A. Ingargiola, Y. Alhadid, S. Y. Chung, X. Michalet, and S. Weiss, “Toward dynamic structural biology: two decades of singer-molexule Förster resonance energy transfer,” Science359(6373), eaan1133 (2018).
[Crossref]

Supplementary Material (1)

NameDescription
Supplement 1       Supplement 1

Data availability

Data underlying the results presented in this paper are not publicly available at this time but may be obtained from the authors upon reasonable request.

Cited By

Optica participates in Crossref's Cited-By Linking service. Citing articles from Optica Publishing Group journals and other participating publishers are listed here.

Alert me when this article is cited.


Figures (4)

Fig. 1.
Fig. 1. (a) Normalized absorption (Abs) and photoluminescence (PL) spectra of QDs donor and Rh101 dye acceptor measured with 400 nm excitation. (b) Absorption spectrum of QDs-Rh101 complexes. (c) Fluorescence (Flu) spectra of QDs-Rh101 complexes under high pressure from 1atm to 0.9G. (d) The ratio of Rh101 fluorescence intensity (F623 nm) to QDs fluorescence intensity (F516 nm) upon compression.
Fig. 2.
Fig. 2. (a) Pressure-dependent chromaticity coordinates of the emissions of QDs-Rh101 complexes. (b) The fluorescent images (dark background) of QDs-Rh101 complexes at 1atm, 0.4Gpa and 0.8Gpa.
Fig. 3.
Fig. 3. (a) Three dimensional TA signals of the CdTe/CdS QDs alone and (b) CdTe/CdS QDs-Rh101 complexes in water solution at 1atm. (c) TA spectra of QDs alone and (d) CdTe/CdS QDs-Rh101 complexes at 1atm. (e) Kinetics of TA spectra of CdTe/CdS QDs alone and CdTe/CdS QDs-Rh101 complexes. The solid lines correspond to the fittings. (f) Schematic representation of the FRET process and Auger recombination process where energy band diagram indicates the transfer of excitons.
Fig. 4.
Fig. 4. (a) Dependence of pressure on the lifetime of the carrier relaxation (${\tau _1}$), (b) FRET process (${\tau _2}$. ), and (c) Auger recombination process (${\tau _3}$). (d) Ratio of Auger recombination process lifetime to FRET process lifetime. (e) Calculated donor-acceptor distance upon compression from 1atm to 0.9Gpa. (f) The number of absorbed acceptor per QDs under pressure from 1atm to 0.9Gpa.

Tables (1)

Tables Icon

Table 1. Summary of the FRET rate (kFRET), spectral overlap J(λ), Förster distance (R0), and possibility (P) of acceptor adsorbed to QDs under several represent pressures.

Equations (5)

Equations on this page are rendered with MathJax. Learn more.

k F R E T = 1 τ D ( R 0 r ) 6
R 0 6 = 9000 ln ( 10 ) k 2 φ D J ( λ ) 128 π 5 N A s 4
r = R 0 ( m ( 1 E ) E ) 1 / 1 6 6
p ( n , λ ) = λ n n ! e λ
λ = ln ( B V / B 0 )

Metrics