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Vibrational strong coupling between Tamm phonon polaritons and organic molecules

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Abstract

Phonon polaritons (PhPs) have a long lifetime and high confinement of light fields compared with their plasmonic counterparts in the mid-infrared range. Thus, PhPs are promising candidates for realizing vibrational strong coupling (VSC) with molecules. However, VSCs of PhPs in nanoresonators and thin films require the near-field technique and are limited to the transverse magnetic mode. Here we propose a new configuration based on the Tamm structure, which supports PhPs excited by the free-space incident light in both transverse-electric and transverse-magnetic modes. The VSC of a 300 nm thick molecular layer can be achieved with $21\,{{\rm cm}^{- 1}}$ Rabi splitting, according to the numerically obtained angle resolved reflectivity spectra with the transfer matrix method. Our findings provide a promising platform for applications in free-space sensing of vibrational modes and control of chemical reactions in compact devices.

© 2021 Optical Society of America

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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.

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