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Mixing of polarization states in zincblende nonlinear optical crystals

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Abstract

We describe second-order nonlinear optical mixing in non-birefringent, zincblende-structure materials that can be quasi-phasematched. Lack of birefringence and quasi-phasematching together allow efficient nonlinear mixing between diverse polarization states. We derive six coupled-wave equations that describe nonlinear optical mixing between the two orthogonal polarizations of the three frequencies in the second-order nonlinear interaction. The interactions of the additional polarization states can lead to apparent reduction in conversion efficiencies in optical parametric oscillators and amplifiers.

© 2018 Optical Society of America under the terms of the OSA Open Access Publishing Agreement

1. Introduction

Zincblende semiconductors such as GaAs, GaP, and ZnSe are attracting increasing attention for nonlinear optical frequency conversion. These materials have large nonlinear susceptibilities and wide transparency ranges extending far into the infrared. Cubic symmetry in zincblende crystals implies isotropic linear optical properties, which means that birefringent phasematching is not possible in bulk media. The difficulty in achieving phasematching in these materials has historically limited their utility. The development of practical techniques to achieve quasi-phasematching (QPM) [1] has enabled more widespread use of zincblende crystals for nonlinear optics. Epitaxial methods of growing crystals with periodically alternating domain orientations have been developed in GaAs [2–4] and GaP [5, 6]. These quasi-phasematched zincblende materials have been used to demonstrate second-harmonic generation (SHG) [7–9], optical parametric oscillation [10–15], difference frequency generation (DFG) [16–20] and optical parametric generation [21].

High symmetry in the nonlinear susceptibility tensor for zincblende crystals combined with the lack of birefringence allow for efficient mixing of a wide range of polarization states. The only non-zero tensor elements in zincblende-structure (4¯3m point group) materials are dxyz and its permutations (namely, dxyz = d14 = d25 = d36 in contracted notation). As a result, one is no longer constrained to choose waves with specific combinations of linear polarization to access the large non-zero coefficient. QPM allows phasematching to be achieved without relying on birefringence and specific polarization states. Using QPM GaAs, polarization-insensitive DFG [16], and optical parametric oscillation using various linearly polarized pump sources [10], as well as circularly polarized and depolarized pump sources [11] were demonstrated.

In this paper, we build on the description of polarization dependence for nonlinear optical mixing in zincblende crystals presented previously [10, 11, 19, 22]. The additional polarization states participating in the nonlinear processes can affect the overall nonlinear conversion efficiency and enhance back-conversion, especially during high gain or depleted pump conditions, such as those occurring in optical parametric oscillators (OPOs) and optical parametric amplifiers (OPAs).

2. Coupled-wave equations

2.1. General driving equations

Assume a collinear interaction and assign the propagation axis to z′ along the propagation direction k^ (which may be different from the crystallographic z^ direction). Typically experiments in QPM zincblende semiconductors like orientation-patterned GaAs (OP-GaAs) and orientation-patterned GaP (OP-GaP) have utilized k^ along the [1¯10] crystallographic direction. We note that propagation along the [001] direction in zincblende materials will produce no nonlinear optical mixing because the non-zero tensor element dxyz requires electric field components along all three crystal directions, x^, y^ and z^. If k^ is parallel to z^ for instance, then there will be no electric field component of any frequency along z^.

In second-order nonlinear mixing between pump (ω3), signal (ω2) and idler (ω1) where ω3 = ω1 + ω2, the electric field at frequency ωi is given by [23]

Ei(z,t)=Re[Ei(z)ei(kizωit)],
where i = 1, 2 or 3 and Ei(z′) is the slowly varying electric field amplitude. Analogous expressions may be written for the nonlinear polarization, Pi(2)(z,t). If each electric field is written in terms of its amplitude and a unit vector in the direction of its polarization, Ei(z)=Eie^i, then Pi(2)(z,t) becomes
P1(2)(z,t)=Re[ϵ0E2 *E3(d__:e^2e^3)ei[(k2+k3)zω1t]]P2(2)(z,t)=Re[ϵ0E1 *E3(d__:e^3e^1)ei[(k1+k3)zω2t]]P3(2)(z,t)=Re[ϵ0E1E2(d__:e^1e^2)ei[(k1+k2)zω3t]].
where (d__:e^2e^3) represents the vector resulting from projection of the tensor d__ on the field directions e^2 and e^3, and similarly for the other two frequencies.

Only the component of the nonlinear polarization transverse to k^ drives the propagating fields. Thus, the slowly varying envelope equations are [23]

dE1(z)dz=iγ1P1,trans(2)(z)eiΔkzdE2(z)dz=iγ2P2,trans(2)(z)eiΔkzdE3(z)dz=iγ3P3,trans(2)(z)eiΔkz,
where Pi,trans(2)(z)=Pi(2)(z)(k^Pi(2)(z))k^, γi = ωi/(2ϵ0cni), and Δk = k3k1k2.

Each of the vector quantities in Ei(z′) and Pi,trans(2)(z) can be projected onto two orthogonal axes transverse to k^. The use of a single Δk in Eq. (3) is appropriate only for isotropic media such as the zincblende semiconductors, or when propagating along an optical axis of a birefringent crystal. What typically happens in birefringent crystals is that only one combination of pump, signal and idler polarizations is phasematched, which enables neglect of the other three field components and thus reduction of Eq. (3) to three scalar equations. However, by using QPM in non-birefringent crystals, phasematching no longer constrains the polarization states that can participate in the interactions so that Eqs. (3) represents six scalar equations instead of three. The dynamics described by these equations can be very rich, some aspects of which we explore in this paper.

2.2. Amplitude and orientation equations

The six coupled-wave equations in Eq. (3) can be cast in terms of the amplitudes and polarization-orientation angles of the interacting waves. In this discussion, we will limit ourselves to linear polarization states and assume isotropic refractive indices. Let us consider linearly polarized, orthogonal unit vectors (a^, b^) in the plane orthogonal to k^. For the typical geometry in OP-GaAs and OP-GaP, k^ is parallel to [1¯10], and the transverse basis can be chosen as a^ along 110 and b^ along [001]. We can write Ei (z′) as

Ei=Eiθ^i,θ^i=cosθia^+sinθib^,
where Ei is the amplitude of the field, θi is the orientation angle of Ei relative to a^. We note that θ^i differ from e^i discussed in section 2.1 in that θ^i are by construction perpendicular to the propagation direction k^ whereas e^i refer to generic electric field polarizations. The derivative of Ei with respect to z′ is
dEidz=ddz(Eiθ^i)=dEidzθ^i+Eidθidzθ^i,,
where θ^i,=sinθia^+cosθib^ is a unit vector orthogonal to θ^i.

Combining Eqs. (3) and (5) and assuming Δk = 0, it follows that

dE1dz=iκ1E2 *E3θ^1(d__:θ^2θ^3)=iκ1E2 *E3f1(θ1;θ2,θ3)dE2dz=iκ2E3E1 *θ^2(d__:θ^3θ^1)=iκ2E3E1 *f2(θ2;θ3,θ1)dE3dz=iκ3E1E2θ^3(d__:θ^1θ^2)=iκ3E1E2f3(θ3;θ1,θ2)E1dθ1dz=iκ1E2 *E3θ^1,(d__:θ^2θ^3)=iκ1E2 *E3f1,(θ1;θ2,θ3)E2dθ2dz=iκ2E3E1 *θ^2,(d__:θ^3θ^1)=iκ2E3E1 *f2,(θ2;θ3,θ1)E3dθ3dz=iκ3E1E2θ^3,(d__:θ^1θ^2)=iκ3E1E2f3,(θ3;θ1,θ2)
where d__=d__/2d36 and κi = 2ϵ0d36γi = ωid36/nic.

In Eq. (6), we define the functions

fi(θi;θj,θk)=θ^i(d__:θ^jθ^k)fi,(θi;θj,θk)=θ^i,(d__:θ^jθ^k).
The fi functions represent the projections of the nonlinear susceptibility tensor onto the field polarization directions. The first three equations in Eq. (6) are the same in structure as the usual three-wave mixing equations, with the strength of the coupling modified by the fi functions. As seen in Eq. (7), calculation of the fi functions is the same calculation as involved in evaluating the effective nonlinear coefficient in the conventional three-wave case. An important difference is that in the six-wave case, the strength of the coupling can change as the polarization states of the interacting waves evolve. The second three equations in Eq. (6) describe the evolution of the angles θi. If θi varies with z′, then the fi will also depend on z′. The evolution of each of the θi is driven by the orthogonal component of the nonlinear polarization, θ^i,P(2)(ωi) or equivalently by fi,⊥. When fi,⊥ is non-zero, the transverse component of the nonlinear polarization, Pi,trans(2) is not parallel to Ei, and so the polarization angle θi will evolve with z′.

The polarization-angle evolution equations in Eq. (6) show that i/dz′ is proportional to 1/Ei, which implies that when the field amplitude at ωi is small, the orientation angle of that field is more easily changed compared to when Ei is large. As a result, we would expect that when a wave has very little power (either at the initial portion of an interaction or when it becomes highly depleted), its orientation angle may change rapidly.

For a down-conversion process where the initial idler field is zero, but E3(0) and E2(0) are non-zero, the idler angle equation dictates that f1,⊥ = 0 at z′ = 0 in order for 1/dz′ to be finite (since 1/dz′ ∝ 1/E1). The condition f1,⊥ = 0 is mathematically identical to the stipulation that θ1 is chosen to maximize the gain (or magnitude of f1) for given θ2 and θ3. Similar considerations apply for a sum-frequency or second-harmonic generation process where E3(0) vanishes.

3. Manley-Rowe relations

Even though the polarization orientation angles of the waves may change, Manley-Rowe relations [23] still apply. The intensity at frequency ωi is given by I(ωi)=ϵ0cniEi*Ei/2, so the change in intensity with respect to z′ is

dI(ωi)dz=ϵ0cni2(Ei*dEidz+EidEi*dz).
If we multiply the three amplitude equations in Eq. (6) by E1*, E2*, and E3*, respectively, add each equation’s complex conjugate, and then compare terms, we see that if
f1(θ1;θ2,θ3)=f2(θ2;θ3,θ1)=f3*(θ3;θ1,θ2)
holds, then the Manley-Rowe relations
1ω1dI(ω1)dz=1ω2dI(ω2)dz=1ω3dI(ω3)dz
are obeyed.

In lossless media, the components of d__ are real quantities [24, 25], and also exhibit full permutation symmetry [24,26]. We only consider linear polarization states and therefore, all fi functions are real. These properties validate Eq. (9), and therefore the Manley-Rowe relations hold. The Manley-Rowe relations can be shown to be obeyed by circular and elliptical polarization states where the fi functions are complex. The proof for complex polarization states and for a general propagation direction in zincblende crystal is given in the Appendix. It is worth noting that a naïve calculation of nonlinear mixing for just one polarization component at each frequency, rather than both as done here, can yield different effective nonlinear coefficients for up-conversion compared to down-conversion, and hence an apparent violation of Manley-Rowe relations (see Appendix B and figure B.1 in [22]).

Eq. (9) simplifies the notation and allows us to write fi(θi; θj, θk = f (θi, θj, θk) = f. Once the function f is derived for a particular propagation geometry, then fi, can be calculated using

fi,(θi;θj,θk)=fθi.
Calculation of the f function is effectively the same as calculating the polarization dependence of deff (as described in [11, 19, 22]). For example, the f and fi,⊥ functions for the case of k^||[1¯10], a^||[110] and b^||[001] in a zincblende crystal are
f=sinθ1cosθ2cosθ3+cosθ1sinθ2cosθ3+cosθ1cosθ2sinθ3f1,=cosθ1cosθ2cosθ3sinθ1sinθ2cosθ3sinθ1cosθ2sinθ3f2,=sinθ1sinθ2cosθ3+cosθ1cosθ2cosθ3cosθ1sinθ2sinθ3f3,=sinθ1cosθ2sinθ3cosθ1sinθ2sinθ3+cosθ1cosθ2cosθ3.
The permutation symmetry among θ1, θ2, and θ3 in f is apparent in the first equation.

For difference frequency generation where the initial angles θ2 and θ3 are fixed, the idler emerges at the angle where f is maximized. By setting ∂ f/∂θ1 = 0 and solving for θ1 in Eq. (12), we find that

tanθ1=cosθ2cosθ3sin(θ2+θ3)f=sin2(θ2+θ3)+cos2θ2cos2θ3=cos2θ2+sin2θ2cos2θ3+2cosθ2cosθ3sinθ2sinθ3.
These agree with expressions for the effective nonlinear coefficient in [19, 22]. Eq. (13) can be applied to sum-frequency generation by interchanging the roles of θ1 and θ3.

4. Effective gain reduction in OPOs and OPAs

The simultaneous phasematching of multiple polarizations in zincblende materials can lead to an apparent reduction in gain and conversion efficiency in nonlinear frequency conversion. The cause of the apparent gain reduction is phasematched back-conversion to a field at the pump frequency but polarized in a direction orthogonal to the original pump. The back-conversion process to the orthogonally polarized pump is an unseeded, cascaded process. In the absence of this process, generation of signal and idler would proceed until the pump becomes depleted, at which point back-conversion of the pump with a 180° phase inversion begins. However, in non-birefringent materials, both pump polarizations are phasematched, and if f3,⊥ ≠ 0, back-conversion of the field at ω3 polarized orthogonally to the original pump will begin as soon as finite amplitudes of the signal and idler fields are present. This back-generated field together with the remaining pump field in the input polarization will manifest as a rotation of the polarization angle of the pump field.

We examine the effective gain reduction associated with polarization-independent phasematching in optical parametric amplification and show the close relationship between gain reduction and polarization rotation. We also look at a plane-wave OPO based on a quasi-phasematched zincblende crystal. The conversion efficiency and output polarization-orientation angles of the OPO differ from those quantities of an OPO with fixed polarization angles.

4.1. Optical parametric amplification

In optical parametric amplification, a strong pump at frequency ω3 amplifies a seed signal at ω2 while producing an idler at ω1 (with ω3 = ω1 + ω2). Let us assume that the pump is undepleted (E3 = E3,0) and that the idler is unseeded (E1(0) = 0). If Δk = 0, we find from Eq. (6)

d2E1dz2=iκ1E3,0(dE2*dzf+E2*(fθ1dθ1dz+fθ2dθ2dz+fθ3dθ3dz))=iκ1E3,0(dE2*dzf+E2*(f1,dθ1dz+f2,dθ2dz+f3,dθ3dz))=E1(κ1κ2|E3,0|2|f|2κ12(E2*)2E3,02E12f1,2κ1κ2E3,02E1*E2*E1E2f2,2κ1κ3|E2|2f3,2).

In the previous section, we argued that if E1(0) = 0, then f1,⊥ = 0 at z′ = 0. We can choose the polarization angle at ω2 to maximize gain, which implies that ∂f/∂θ2 = f2,⊥ = 0 at z′ = 0. In the low-conversion limit, we may approximate that f1,⊥ ≈ 0 and f2,⊥ ≈ 0 over the entire propagation length. With these simplifying assumptions, the last expression in Eq. (14) becomes

d2E1dz=E1(κ1κ2|E3,0|2|f|2κ1κ3|E2|2f3,2).
Using similar arguments for the amplification of the signal at ω2, we find
d2E2dz2=E2(κ1κ2|E3,0|2|f|2κ2κ3|E1|2f3,2).

In Eqs. (15) and (16), we can identify κ1κ2|E3,0||f| as the OPA gain coefficient in the absence of polarization rotation. The second term on the right-hand sides of Eqs. (15) and (16) involving f3,⊥ are associated with back-conversion to the orthogonally polarized pump, which is manifested as rotation of the pump polarization from the initial orientation and reduction of the net OPA gain coefficient. Note that the gain reduction for E1 depends on the magnitude of the input signal compared to the pump. The reduction in gain for E2 depends on the magnitude of E1 compared to E3,0; |E1| is small since we are assuming low-conversion and that the idler is initially unseeded, so the evolution of E2 will be dominated by the first term in Eq. (16). As the signal and idler grow with z′, the deviations in gain increase, ultimately violating the assumption of small pump depletion.

4.2. Optical parametric oscillation

The gain and conversion efficiencies in optical parametric oscillators based on QPM zincblende materials will also be affected by phasematched back-conversion and evolution of the polarization angles. To frame the discussion, let us first recall a simple model of a phasematched (Δk = 0), plane-wave, singly resonant OPO with low loss and low outcoupling, and single polarization states at the pump, signal and idler [27]. Eq. (6) suggests that the expressions in [27] can to first order be modified to include polarization-dependent gain by the substitution κiκi f. Thus, the gain in an OPO is related to the times above threshold, N, by

N=(E3(0)E3,th(0))2=κ1κ2f2E3(0)2L2as=1sinc2βL,
where E3(0) is the pump amplitude at the crystal entrance, E3,th(0 is the pump amplitude at oscillation threshold, L is the crystal length, as is the round-trip power loss at the signal, and
β=κ1κ3E2f.

This plane-wave OPO model assumes that variation in E2 with z′ is small, which is appropriate for steady-state operation of a low-loss, low out-coupling OPO. The pump will be depleted according to

PD=I3(0)I3(L)I3(0)=sin2βL,
where PD represents pump depletion. If we assume all of the loss is from outcoupling (as = 1−R), then the external signal photon conversion efficiency, η2=(1R)ω3I2(L)/(ω2I3(0)) is η2=(βL)2/N=PD. The problem with this model for non-birefringent media is that it does not account for the existence of polarization diversity in the six-wave interactions. f and β are not constant inside the OPO. The following numerical example illustrates the polarization rotation effects.

To examine these issues quantitatively, we compared the model that neglects polarization rotation effects to numerical modeling of a QPM zincblende OPO pumped at two times above threshold (N = 2) and where all the losses are from outcoupling. For N = 2, an OPO will have conversion efficiency predicted by the above equations of η2=96.8%. We performed the OPO simulation by integrating Eq. (6) over many roundtrips with appropriate boundary conditions and different initial pump polarization angles. We assumed 100% transmission of the pump and 100% reflection of the signal at the input coupler; 100% transmission of the pump and idler, and (1 − R) = 0.3% transmission of the signal at the output coupler. We chose this low outcoupling for convenient comparison to the analytical low-loss results. The crystal was assumed to be lossless, and the sample geometry was k^||[1¯10], a^||[110] and b^||[001]. In the our calculations, we first calculated the optimal angles (θ1,opt, θ2,opt) that maximized f for a given pump orientation θ3 and hence the gain at threshold where cascading effects are absent. Eq. (18) allowed us to estimate E2 for given N and f (θ3, θ1,opt, θ2,opt). These optimal angles would be the polarizations expected from Eq. (12) if there were no polarization rotation effects. We used the optimal angles and the estimate for E2 as initial guesses for the OPO, then numerically propagated over many round trips until steady-state amplitudes and polarization angles were reached. Since E1 = 0 at the input of the crystal, we assumed the idler takes on the polarization orientation that optimizes f given the input pump polarization and the signal polarization found from the previous round trip.

Figure 1 shows results of the numerical modeling with the input pump polarized at 45° to [110]. The optimal signal and idler polarization angles that maximize f (and thus the effective nonlinearity) are θ1,opt = θ2,opt = 31.72°. The plots show the steady-state intensities and polarization angles of the OPO as a function of position inside the nonlinear crystal as well as the evolution of the f function. The simulations in Fig. 1 show that the steady-state signal polarization angle was 29.593° and η2=96.0%. The polarization angle of the pump is significantly different at the exit of the crystal compared to the input (66.1° vs. 45°), which is an effect related to back-conversion to the orthogonally polarized pump.

 figure: Fig. 1

Fig. 1 Numerical modeling of a zincblende OPO including polarization rotation for the case of N = 2, 0.3% output coupling and pump polarization θ3(0) = 45° to [110]. The top row (a)–(c) shows the relative intensities, the second row (d)-(f) shows the polarization angles, and the last row (g) shows the evolution of the function f as a function of crystal location.

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To see the effects at different input pump polarization angles, we ran a family of simulations with fixed times above threshold. The f (θ3, θ1,opt, θ2,opt) parameter varied with different input pump polarization angles, and hence from Eq. (17), we had to adjust the input pump intensity in order to hold N constant. Figure 2 plots external signal conversion efficiency for several different input pump polarizations with N = 2 in the OPO simulations. We see in Fig. 2 that the conversion efficiencies are generally reduced. When the pump is polarized along [001] (90°) or along [111] (35.3°), the conversion efficiency match the fixed-angle cases; at these special orientations, the fi,⊥ functions go to zero and hence the polarization angles do not change. When the pump angle tends towards 0°, the conversion efficiencies for the simulations also approach the fixed-angle result, 96.8%. θ3 = 0° corresponds to the interesting case of [110] pumping, which we discuss in greater detail later.

 figure: Fig. 2

Fig. 2 Signal photon conversion efficiency, η2, as a function of pump angle for fixed times above threshold (N = 2). As comparison, the solid line plots the prediction with the polarization angles fixed to maximize the gain at threshold.

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The output polarization-orientation angles in the OPO differ from optimal angles θi,opt we expect from simply maximizing f. Fig. 3 shows the output polarization angles if the polarization rotation effects are included compared to θ1,opt, θ2,opt and θ3,in. Figure 4 shows the deviations of the simulated output angles relative to the angles expected in the absence of polarization rotation. For the pump, Δθ3 is the calculated output pump angle minus the input pump angle, and for the signal and idler, Δθi = θi,simθi,opt. It should be noted that the θi,opt are not necessarily the same as the polarization angles at z′/L = 0 because the steady-state OPO incorporates angular changes of the signal and idler, even at z′/L = 0 (examples of this effect are illustrated in Figs. 1(d) and 1(e)).

 figure: Fig. 3

Fig. 3 Comparison of polarization angles at the output of the OPO if the polarization rotation effects are neglected (θi,opt, solid line) or included (θi,sim, open circles) for N = 2.

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 figure: Fig. 4

Fig. 4 Deviation of polarization angles (θi,simθi,opt) for different initial pump angle in a zincblende OPO with times above threshold, N = 2.

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Comparing Figs. 2 and 4, we see a correlation between the decrease in OPO conversion efficiency and the magnitude of pump-angle change, |Δθ3|. When the pump is polarized along [001] or [111], the pump, signal and idler polarizations do not rotate away from the expected angles, and there is no decrease η2 between the varying- and fixed-angle cases. As the pump approaches [110] polarization, the signal and idler angles deviate increasingly from θi,opt. At θ3 = 0°, θ1,opt = θ2,opt = 45°, but the OPO simulations instead show that θ1 → 0° and θ2 → 90°.

We also looked at simulation results at different times above threshold, N. These results as a function of N for three different incident pump polarization angles are presented in Fig. 5. Of the three cases, the conversion efficiencies were highest for θ3(0) = 90° where the polarizations do not evolve, which was also seen in Fig. 2. Other pump polarization angles show reduced conversion efficiency, but as shown in Fig. 5(a), the reduction is modest. As N approaches (π/2)2 = 2.47 where full conversion is expected in a low-loss OPO [27], the pump becomes strongly depleted and we observe large changes in the pump polarization angles (Fig. 5(b)). The signal and idler polarization angles also change more at large N (see in Figs. 5(c) and 5(d)). The magnitudes of the changes in θ1 and θ2 depend on θ3(0).

 figure: Fig. 5

Fig. 5 Dependence on times above threshold, N, of (a) photon conversion efficiency and (b) deviation in pump polarization angle for several incident pump polarization angles. (1 − R) is set to 0.003. The signal and idler output polarization angles for (c) 45° and (d) 10° incident pump polarization angles.

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We also examined the dependence of the zincblende OPO on outcoupling rate, (1 − R), while still assuming as = 1 − R. Figure 6 plots the dependence of the photon conversion efficiency and the output pump polarization angle on N for 1 − R = 0.003, 0.12, and 0.5. The incident pump polarization angle was set to θ3(0) = 10° in these simulations. There is a slight increase in η2 with increasing outcoupling rate. Larger (1 − R) also produced larger deviations in pump polarization angles. Interestingly, changing (1 − R) did not affect the signal and idler polarization angles much, with simulation results for θ1 and θ2 almost identical to those shown in Fig. 5(d). We also looked at cases where OPO loss arose from both outcoupling and absorption loss at at the signal (that is, as > 1 − R) and found the output intensities and polarization angles essentially depended only on the total round-trip loss and not on whether the loss was from absorption in the nonlinear medium or occurred at the output coupler.

 figure: Fig. 6

Fig. 6 Dependence on N of (a) photon conversion efficiency and (b) deviation in pump polarization angle for θ3(0) = 10° and several different outcoupling rates.

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5. Parametric processes with [110]-polarized pump

Pumping a parametric process in a QPM zincblende crystal with [110]-linearly-polarized light and k^||[1¯10] leads to interesting polarization effects. It has been noted in [10, 11, 16] that if the pump is exactly polarized along [110], then the gain becomes independent of the signal polarization, which is the basis for polarization-independent optical parametric amplification [16]. In this section, we examine [110]-polarized pumping in more detail.

Consider a down-conversion process where the pump is polarized along [110] (θ3 = 0°). Assuming that f1,⊥ = 0 (which follows from choosing the idler polarization θ1 to maximize gain), we can solve the second equation in Eq. (12) for θ1 as a function of θ2 and find that

tanθ1=cotθ2.
Substituting this result for θ1 back in expressions in Eq. (12) for f, f2,⊥ and f3,⊥, we find
|f|=1,f2,=0,f3,=12sin2θ2.
Together, Eqs. (20) and (21) show that in [110]-pumped down-conversion, the small-signal gain (proportional to f2) is independent of the signal polarization angle θ2. Eq. (20) implies that the idler will be polarized complementarily to the signal. Furthermore, f2,⊥ = 0 automatically for this combination of signal and idler polarizations.

Equation (21) indicates that unless the signal polarization, θ2, is 0°, 90°, etc., f3,⊥ is non-zero and therefore the pump polarization will evolve away from [110] during propagation in the crystal. As θ3 deviates from 0°, the function f and the gain are no longer independent of θ2. f will evolve with z′ in cases of significant pump depletion, unless θ2 = 0°, 90°, etc. However, in optical parametric amplifiers where the pump power remains undepleted and much larger than either the signal or idler powers, the change of pump polarization will be small since |3/dz′| is proportional to |E1E2/E3|. Also, when θ3 is near 0°, f is only weakly dependent on θ2, so the gain in down-conversion can be nearly (but not quite) independent of θ2.

The gain in a [110]-pumped down-conversion process is identical when the signal polarization is along [110] or along [001]. With these polarization angles, fi,⊥ = 0 for all waves (including the pump), so the angles will remain fixed during propagation in the crystal. Such a device is of interest for signal-processing functions such as dual-polarization wavelength conversion since two orthogonally polarized signal waves can be converted with the same efficiencies. Identical conversion efficiencies for TE and TM polarizations were demonstrated using AlGaAs waveguides in [16]. However, signal waves polarized at angles other than θ2 = 0° or 90° will experience slightly different gains as f3,⊥ and 3/dz′ are no longer zero.

The analysis presented here suggests that a [110]-pumped OPO is equally likely to oscillate with (θ1, θ2) equal to (0°, 90°) or (90°, 0°). At these angles, fi,⊥ = 0 so the polarization-orientation angles do not evolve in the OPO, which explains why the simulated conversion efficiencies near θ3 = 0° in Fig. 2 approach the fixed-angle η2 values. The OPO is less likely to oscillate with other angular combinations since the net gain is lower due to f3,⊥ ≠ 0. The OPO essentially exhibits “polarization eigenstates” where it stably oscillates with equal efficiency at (θ1, θ2) = (0°, 90°) and (90°, 0°). Since θ2 = 0° and 90° mix equally well with the [110]-polarized pump, it should be possible to insert a half-wave plate inside an OPO cavity in a ring configuration (quarter-wave plate for a standing-wave OPO cavity) that rotates the polarization of the resonating signal wave by 90° on each round trip. The light will make two trips around the cavity to complete one round trip with amplification occurring on both trips through the crystal.

6. Applications and future work

The nonlinear optical processes described above are just a few examples of the interesting polarization dynamics arising from χ(2) mixing in QPM zincblende crystals. When all polarization states are phasematched to require six rather than three coupled-wave equations (described in Sections 2 and 3), the interactions of the additional three waves have similarities to simultaneously phasematched processes, such as cascaded sum-frequency generation [21] or other multistep parametric processes [28]. Most previous work on multistep processes has involved birefringent crystals such as PPLN or KTP. In these previous treatments of mixing of different polarization states, the discussions have typically involved multiple phase-mismatch factors or have ignored interactions of certain polarizations that are far away from phasematching. When mixing polarization states in a QPM zincblende crystal, the coupling coefficients for different polarization combinations can be similar in magnitude because of the highly symmetric nonlinear susceptibility tensor and the fact that there are no constraints from phasematching on which polarization states can interact. Hence it may be interesting to investigate nonlinear mixing in QPM zincblende semiconductors for the effects of all-optical signal processing through polarization switching [29–31].

7. Conclusion

Quasi-phasematching has allowed efficient nonlinear optical frequency conversion in bulk, isotropic media such as zincblende semiconductors. In these non-birefringent systems, χ(2) mixing is described by six rather than three coupled-wave equations since both polarization states at each of the three frequencies can participate in the interaction. The six coupled-wave equations can be cast in terms of amplitudes and polarization angles, which are similar in mathematical structure to the amplitude and phase equations in conventional three-wave mixing [23, 24]. Cascaded conversion into orthogonal polarization states can act like parasitic processes. We show that these cascaded processes can reduce conversion efficiencies in optical parametric oscillators and amplifiers based on QPM zincblende materials. Simultaneously phasematched processes in zincblende semiconductors lead to rich and complicated polarization dynamics with many opportunities for further exploration.

Appendix. Manley-Rowe relations for general polarization states

The Manley-Rowe relations, dictating the exchange of energy in photon units, must be obeyed in cubic crystals as in any other case, though proper framing of the relation for isotropic media requires somewhat more care. If a single vector component of each field is considered at each frequency, as is the case in conventional birefringent media, apparent violations of the Manley-Rowe relations can emerge; both transverse vector components of the field must be considered in evaluating the effective nonlinear coefficient, and the change in that coefficient as the polarization states evolve must be taken into account. Care must also be taken when using a complex basis, e.g. circular polarizations, for describing the polarization states of the fields.

To illustrate these points, we derive the Manley-Rowe relations in a form suitable for isotropic media, and with possibly complex polarization bases. We define the basis vectors orthogonal to propagation direction k^ as [a^,b^], where

a^=iaii^b^=ibii^a^a^*=b^b^*=1a^b^*=0.
The unit vectors i^ represent the Cartesian directions (x^,y^,z^), and the ai and bi coefficients may be complex. Examining Eqs. (10), (8) and (3), it is straightforward to show that the Manley-Rowe relations require that
(E3*P3+E3P3*)=(E2*P2+E2P2*)=(E1*P1+E1P1*).
Here, we use Ei and Pi to represent Ei(z′) and P(2)(z′), respectively. With the constitutive relations given by Eq. (2), Eq. (23) can be shown to require that
E3*(d__:E^1E^2)=E2(d__:E^3E^1*)*=E1(d__:E^2*E^3)*.
Expanding the fields for the first relation in Eq. (24) using the basis described in Eq. (22), we obtain
i[(E3,a*ai*+E3,b*bi*)j,kdijk(ω3;ω1,ω2)(E1,aaj+E1,bbj)(E2,aak+E1,bbk)]=k{(E2,aak+E1,bbk)[i,jdkij(ω2;ω3,ω1)(E3,aai+E3,bbi)(E1,a*aj*+E1,b*bj*)]*}.
Recalling that d__(ω)=d__*(ω), and in lossless media, d__ is real and obeys overall permutation symmetry, it follows that dkij*(ω2;ω3,ω1)=dkij(ω2;ω3,ω1)=dijk(ω3;ω1,ω2) and we see that the equality in Eq. (25) is satisfied. The other equalities required for Eq. (23) can be shown similarly to hold. It can also be seen how the equalities can fail if only a single component of each field were considered, and that care must be taken for consistent use of complex polarization bases.

Funding

Air Force Office of Scientific Research (FA9550-09-1-0233).

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Figures (6)

Fig. 1
Fig. 1 Numerical modeling of a zincblende OPO including polarization rotation for the case of N = 2, 0.3% output coupling and pump polarization θ3(0) = 45° to [110]. The top row (a)–(c) shows the relative intensities, the second row (d)-(f) shows the polarization angles, and the last row (g) shows the evolution of the function f as a function of crystal location.
Fig. 2
Fig. 2 Signal photon conversion efficiency, η 2 , as a function of pump angle for fixed times above threshold (N = 2). As comparison, the solid line plots the prediction with the polarization angles fixed to maximize the gain at threshold.
Fig. 3
Fig. 3 Comparison of polarization angles at the output of the OPO if the polarization rotation effects are neglected (θi,opt, solid line) or included (θi,sim, open circles) for N = 2.
Fig. 4
Fig. 4 Deviation of polarization angles (θi,simθi,opt) for different initial pump angle in a zincblende OPO with times above threshold, N = 2.
Fig. 5
Fig. 5 Dependence on times above threshold, N, of (a) photon conversion efficiency and (b) deviation in pump polarization angle for several incident pump polarization angles. (1 − R) is set to 0.003. The signal and idler output polarization angles for (c) 45° and (d) 10° incident pump polarization angles.
Fig. 6
Fig. 6 Dependence on N of (a) photon conversion efficiency and (b) deviation in pump polarization angle for θ3(0) = 10° and several different outcoupling rates.

Equations (25)

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E i ( z , t ) = Re [ E i ( z ) e i ( k i z ω i t ) ] ,
P 1 ( 2 ) ( z , t ) = Re [ ϵ 0 E 2   * E 3 ( d _ _ : e ^ 2 e ^ 3 ) e i [ ( k 2 + k 3 ) z ω 1 t ] ] P 2 ( 2 ) ( z , t ) = Re [ ϵ 0 E 1   * E 3 ( d _ _ : e ^ 3 e ^ 1 ) e i [ ( k 1 + k 3 ) z ω 2 t ] ] P 3 ( 2 ) ( z , t ) = Re [ ϵ 0 E 1 E 2 ( d _ _ : e ^ 1 e ^ 2 ) e i [ ( k 1 + k 2 ) z ω 3 t ] ] .
d E 1 ( z ) d z = i γ 1 P 1 , trans ( 2 ) ( z ) e i Δ k z d E 2 ( z ) d z = i γ 2 P 2 , trans ( 2 ) ( z ) e i Δ k z d E 3 ( z ) d z = i γ 3 P 3 , trans ( 2 ) ( z ) e i Δ k z ,
E i = E i θ ^ i , θ ^ i = cos θ i a ^ + sin θ i b ^ ,
d E i d z = d d z ( E i θ ^ i ) = d E i d z θ ^ i + E i d θ i d z θ ^ i , ,
d E 1 d z = i κ 1 E 2   * E 3 θ ^ 1 ( d _ _ : θ ^ 2 θ ^ 3 ) = i κ 1 E 2   * E 3 f 1 ( θ 1 ; θ 2 , θ 3 ) d E 2 d z = i κ 2 E 3 E 1   * θ ^ 2 ( d _ _ : θ ^ 3 θ ^ 1 ) = i κ 2 E 3 E 1   * f 2 ( θ 2 ; θ 3 , θ 1 ) d E 3 d z = i κ 3 E 1 E 2 θ ^ 3 ( d _ _ : θ ^ 1 θ ^ 2 ) = i κ 3 E 1 E 2 f 3 ( θ 3 ; θ 1 , θ 2 ) E 1 d θ 1 d z = i κ 1 E 2   * E 3 θ ^ 1 , ( d _ _ : θ ^ 2 θ ^ 3 ) = i κ 1 E 2   * E 3 f 1 , ( θ 1 ; θ 2 , θ 3 ) E 2 d θ 2 d z = i κ 2 E 3 E 1   * θ ^ 2 , ( d _ _ : θ ^ 3 θ ^ 1 ) = i κ 2 E 3 E 1   * f 2 , ( θ 2 ; θ 3 , θ 1 ) E 3 d θ 3 d z = i κ 3 E 1 E 2 θ ^ 3 , ( d _ _ : θ ^ 1 θ ^ 2 ) = i κ 3 E 1 E 2 f 3 , ( θ 3 ; θ 1 , θ 2 )
f i ( θ i ; θ j , θ k ) = θ ^ i ( d _ _ : θ ^ j θ ^ k ) f i , ( θ i ; θ j , θ k ) = θ ^ i , ( d _ _ : θ ^ j θ ^ k ) .
d I ( ω i ) d z = ϵ 0 c n i 2 ( E i * d E i d z + E i d E i * d z ) .
f 1 ( θ 1 ; θ 2 , θ 3 ) = f 2 ( θ 2 ; θ 3 , θ 1 ) = f 3 * ( θ 3 ; θ 1 , θ 2 )
1 ω 1 d I ( ω 1 ) d z = 1 ω 2 d I ( ω 2 ) d z = 1 ω 3 d I ( ω 3 ) d z
f i , ( θ i ; θ j , θ k ) = f θ i .
f = sin θ 1 cos θ 2 cos θ 3 + cos θ 1 sin θ 2 cos θ 3 + cos θ 1 cos θ 2 sin θ 3 f 1 , = cos θ 1 cos θ 2 cos θ 3 sin θ 1 sin θ 2 cos θ 3 sin θ 1 cos θ 2 sin θ 3 f 2 , = sin θ 1 sin θ 2 cos θ 3 + cos θ 1 cos θ 2 cos θ 3 cos θ 1 sin θ 2 sin θ 3 f 3 , = sin θ 1 cos θ 2 sin θ 3 cos θ 1 sin θ 2 sin θ 3 + cos θ 1 cos θ 2 cos θ 3 .
tan θ 1 = cos θ 2 cos θ 3 sin ( θ 2 + θ 3 ) f = sin 2 ( θ 2 + θ 3 ) + cos 2 θ 2 cos 2 θ 3 = cos 2 θ 2 + sin 2 θ 2 cos 2 θ 3 + 2 cos θ 2 cos θ 3 sin θ 2 sin θ 3 .
d 2 E 1 d z 2 = i κ 1 E 3 , 0 ( d E 2 * d z f + E 2 * ( f θ 1 d θ 1 d z + f θ 2 d θ 2 d z + f θ 3 d θ 3 d z ) ) = i κ 1 E 3 , 0 ( d E 2 * d z f + E 2 * ( f 1 , d θ 1 d z + f 2 , d θ 2 d z + f 3 , d θ 3 d z ) ) = E 1 ( κ 1 κ 2 | E 3 , 0 | 2 | f | 2 κ 1 2 ( E 2 * ) 2 E 3 , 0 2 E 1 2 f 1 , 2 κ 1 κ 2 E 3 , 0 2 E 1 * E 2 * E 1 E 2 f 2 , 2 κ 1 κ 3 | E 2 | 2 f 3 , 2 ) .
d 2 E 1 d z = E 1 ( κ 1 κ 2 | E 3 , 0 | 2 | f | 2 κ 1 κ 3 | E 2 | 2 f 3 , 2 ) .
d 2 E 2 d z 2 = E 2 ( κ 1 κ 2 | E 3 , 0 | 2 | f | 2 κ 2 κ 3 | E 1 | 2 f 3 , 2 ) .
N = ( E 3 ( 0 ) E 3 , t h ( 0 ) ) 2 = κ 1 κ 2 f 2 E 3 ( 0 ) 2 L 2 a s = 1 sinc 2 β L ,
β = κ 1 κ 3 E 2 f .
PD = I 3 ( 0 ) I 3 ( L ) I 3 ( 0 ) = sin 2 β L ,
tan θ 1 = cot θ 2 .
| f | = 1 , f 2 , = 0 , f 3 , = 1 2 sin 2 θ 2 .
a ^ = i a i i ^ b ^ = i b i i ^ a ^ a ^ * = b ^ b ^ * = 1 a ^ b ^ * = 0 .
( E 3 * P 3 + E 3 P 3 * ) = ( E 2 * P 2 + E 2 P 2 * ) = ( E 1 * P 1 + E 1 P 1 * ) .
E 3 * ( d _ _ : E ^ 1 E ^ 2 ) = E 2 ( d _ _ : E ^ 3 E ^ 1 * ) * = E 1 ( d _ _ : E ^ 2 * E ^ 3 ) * .
i [ ( E 3 , a * a i * + E 3 , b * b i * ) j , k d i j k ( ω 3 ; ω 1 , ω 2 ) ( E 1 , a a j + E 1 , b b j ) ( E 2 , a a k + E 1 , b b k ) ] = k { ( E 2 , a a k + E 1 , b b k ) [ i , j d k i j ( ω 2 ; ω 3 , ω 1 ) ( E 3 , a a i + E 3 , b b i ) ( E 1 , a * a j * + E 1 , b * b j * ) ] * } .
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