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Physical Review A

Study of ultra-fast relaxation processes by resonant Rayleigh-type optical mixing. I. Theory

Tatsuo Yajima, Hirotoshi Souma

Published Jan 1, 1978• 146 citations
Publisher

Abstract

A comprehensive theory of a new type of three-wave optical mixing (${\ensuremath{\omega}}_{3}=2{\ensuremath{\omega}}_{1}\ensuremath{-}{\ensuremath{\omega}}_{2}$) is given for the spectroscopic purpose of determining ultra-short relaxation times (picoseconds or less) associated with excited states of condensed matter. Two incident light frequencies ${\ensuremath{\omega}}_{1}$ and ${\ensuremath{\omega}}_{2}$ are chosen so that they are both resonant with an inhomogeneously broadened optical transition and $|{\ensuremath{\omega}}_{2}\ensuremath{-}{\ensuremath{\omega}}_{1}|$ is in the vicinity of inverse relaxation times. The theory is developed for its major application to broad-band electronic transitions. The nonlinear susceptibility ${\ensuremath{\chi}}_{R}^{(3)}$ for this process (named resonant Rayleigh-type mixing) is calculated by a density-matrix formalism with the model of a two-level atomic system incorporating the distribution of resonance frequencies and longitudinal (${T}_{1}$) and transverse (${T}_{2}$) relaxation times. The result shows a frequency characteristic depending only on ${T}_{1}$, ${T}_{2}$, and ${\ensuremath{\omega}}_{2}\ensuremath{-}{\ensuremath{\omega}}_{1}$ in a broad-band limit, which serves for the determination of ${T}_{1}$ and ${T}_{2}$ in the frequency domain. The analysis is further extended to include the various effects as follows. The calculation of the saturation effect in the lowest order reveals that it modifies the shape of the frequency characteristic of the nonlinear susceptibility but does not affect seriously the determination of relaxation times. The effect of spectral cross relaxation within the inhomogeneous broadening is incorporated by a generalized density-matrix formalism. The resultant ${\ensuremath{\chi}}_{R}^{(3)}$ consists of two terms. The dominant term is the same as before except that ${T}_{1}$ is replaced by a combined relaxation time ${T}_{1}^{\ensuremath{'}}={({T}_{1}^{\ensuremath{-}1}+{T}_{3}^{\ensuremath{-}1})}^{\ensuremath{-}1}$, where ${T}_{3}$ is the cross-relaxation time. The other term originates from the inverse spectral-diffusion process. The effect of other energy levels located between the two levels under study is analyzed with a simple three-level model. The resultant ${\ensuremath{\chi}}_{R}^{(3)}$ also consists of two terms, the dominant one being the same as that for the two-level model except that ${T}_{1}^{\ensuremath{-}1}$ should be interpreted as total population decay rate of the upper level. For accurate derivation of ${\ensuremath{\chi}}_{R}^{(3)}$ from experiment, we discuss the interference between the resonant and nonresonant susceptibility terms and the light-wave propagation effect. Finally, the close analogy between this type of optical mixing and the photon echo is discussed.

DOI
10.1103/physreva.17.309

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High-order effects in Rayleigh-type optical mixing

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A comprehensive theory of a new type of three-wave optical mixing (\ensuremathω3=2\ensuremathω1\ensuremath−\ensuremathω2{\ensuremath{\omega}}_{3}=2{\ensuremath{\omega}}_{1}\ensuremath{-}{\ensuremath{\omega}}_{2}\ensuremathω3​=2\ensuremathω1​\ensuremath−\ensuremathω2​) is given for the spectroscopic purpose of determining ultra-short relaxation times (picoseconds or less) associated with excited states of condensed matter. Two incident light frequencies \ensuremathω1{\ensuremath{\omega}}_{1}\ensuremathω1​ and \ensuremathω2{\ensuremath{\omega}}_{2}\ensuremathω2​ are chosen so that they are both resonant with an inhomogeneously broadened optical transition and ∣\ensuremathω2\ensuremath−\ensuremathω1∣|{\ensuremath{\omega}}_{2}\ensuremath{-}{\ensuremath{\omega}}_{1}|∣\ensuremathω2​\ensuremath−\ensuremathω1​∣ is in the vicinity of inverse relaxation times. The theory is developed for its major application to broad-band electronic transitions. The nonlinear susceptibility \ensuremathχR(3){\ensuremath{\chi}}_{R}^{(3)}\ensuremathχR(3)​ for this process (named resonant Rayleigh-type mixing) is calculated by a density-matrix formalism with the model of a two-level atomic system incorporating the distribution of resonance frequencies and longitudinal (T1{T}_{1}T1​) and transverse (T2{T}_{2}T2​) relaxation times. The result shows a frequency characteristic depending only on T1{T}_{1}T1​, T2{T}_{2}T2​, and \ensuremathω2\ensuremath−\ensuremathω1{\ensuremath{\omega}}_{2}\ensuremath{-}{\ensuremath{\omega}}_{1}\ensuremathω2​\ensuremath−\ensuremathω1​ in a broad-band limit, which serves for the determination of T1{T}_{1}T1​ and T2{T}_{2}T2​ in the frequency domain. The analysis is further extended to include the various effects as follows. The calculation of the saturation effect in the lowest order reveals that it modifies the shape of the frequency characteristic of the nonlinear susceptibility but does not affect seriously the determination of relaxation times. The effect of spectral cross relaxation within the inhomogeneous broadening is incorporated by a generalized density-matrix formalism. The resultant \ensuremathχR(3){\ensuremath{\chi}}_{R}^{(3)}\ensuremathχR(3)​ consists of two terms. The dominant term is the same as before except that T1{T}_{1}T1​ is replaced by a combined relaxation time T1\ensuremath′=(T1\ensuremath−1+T3\ensuremath−1)\ensuremath−1{T}_{1}^{\ensuremath{'}}={({T}_{1}^{\ensuremath{-}1}+{T}_{3}^{\ensuremath{-}1})}^{\ensuremath{-}1}T1\ensuremath′​=(T1\ensuremath−1​+T3\ensuremath−1​)\ensuremath−1, where T3{T}_{3}T3​ is the cross-relaxation time. The other term originates from the inverse spectral-diffusion process. The effect of other energy levels located between the two levels under study is analyzed with a simple three-level model. The resultant \ensuremathχR(3){\ensuremath{\chi}}_{R}^{(3)}\ensuremathχR(3)​ also consists of two terms, the dominant one being the same as that for the two-level model except that T1\ensuremath−1{T}_{1}^{\ensuremath{-}1}T1\ensuremath−1​ should be interpreted as total population decay rate of the upper level. For accurate derivation of \ensuremathχR(3){\ensuremath{\chi}}_{R}^{(3)}\ensuremathχR(3)​ from experiment, we discuss the interference between the resonant and nonresonant susceptibility terms and the light-wave propagation effect. Finally, the close analogy between this type of optical mixing and the photon echo is discussed.
The dispersion characteristics of the nonlinear susceptibility χ ( n ) ( n =3, 5, 7) describing a new type of optical mixing have been calculated for their application to the study of ultra-fast relaxation dynamics in resonant media. The process is that two incident light waves at frequencies ω 1 and ω 2 produce new light waves at ω 1 - m ε and ω 1 + n ε ( ε =ω 2 -ω 1 ; m , n =1, 2, 3, …) under the conditions of two-photon resonance (2ω 1 , 2ω 2 ≃optical transition frequency) and Rayleigh-type resonance (|ω 1 -ω 2 |≃relaxation rate). Results of analysis based on an inhomogeneously broadened three-level model revealed that Rayleigh-type dispersions involving the longitudinal and transverse relaxation rates appear in χ ( n ) ( n ≧5) and χ ( n ) ( n ≧7), respectively. Their analogy with two-photon resonant photon echo and various precautions in applying them to actual situations are also discussed.
The resonant nonlinear-optical phenomenon in condensed matter due to two-frequency excitation is investigated by a first-principles theory without using the phenomenological relaxation-time description. A new generalized nonlinear susceptibility is introduced in order to describe the non-Markovian process in the condensed phase associated with the resonant four-photon parametric effect. It is shown that the present non-Markovian version of the theory of the resonant Rayleigh-type optical mixing (RROM) naturally includes the resonant coherent anti-Stokes Raman scattering (RCARS) as the memory effect of the reservoir. That is, the two phenomena PROM and RCARS are unified from the microscopic viewpoint. The general expressions for nonlinear susceptibility for RROM and RCARS are obtained by taking into consideration the frequency dependence of the transverse relaxation time T2{T}_{2}T2​. These provide us the general guide for the study of several relaxation phenomena in condensed materials by means of resonant coherent nonlinear-optical methods.
A new method of picosecond and femtosecond transient spectroscopy yielding information about ultrafast relaxation processes without requiring ultrashort light pulses is presented. It is based on the present theoretical analysis of the resonant degenerate four-wave-mixing process excited by two temporally incoherent light beams with wave vectors ${\stackrel{\ensuremath{\rightarrow}}{\mathrm{k}}}_{1}$ and ${\stackrel{\ensuremath{\rightarrow}}{\mathrm{k}}}_{2}$ which are originated from a single beam at frequency $\ensuremath{\omega}$ but have mutual time delay $\ensuremath{\tau}$. Under the assumption that the incoherent light field has Gaussian random complex amplitude and that the resonant material consists of the usual two-level atoms, the statistically averaged intensity of the output light field with ${\stackrel{\ensuremath{\rightarrow}}{\mathrm{k}}}_{3}=2{\stackrel{\ensuremath{\rightarrow}}{\mathrm{k}}}_{2}\ensuremath{-}{\stackrel{\ensuremath{\rightarrow}}{\mathrm{k}}}_{1}$ at $\ensuremath{\omega}$ is calculated as a function of $\ensuremath{\tau}$. Even with the light having a much longer duration than both T1{T}_{1}T1​ (the longitudinal relaxation time) and T2{T}_{2}T2​ (the transverse relaxation time), the correlation trace, i.e., output intensity versus $\ensuremath{\tau}$, represents a decay profile determined mainly by T2{T}_{2}T2​ for both homogeneously and inhomogeneously broadened transitions, as long as the light correlation time ${\ensuremath{\tau}}_{c}$ is much shorter than the relaxation times. The correlation trace does not always represent a single-exponential decay but is sometimes slightly deformed by the T1{T}_{1}T1​ effect. However, it does not cause a significant error in the determination of T2{T}_{2}T2​. Moreover, as $\frac{{T}_{2}}{{T}_{1}}\ensuremath{\rightarrow}0$, the trace becomes a single-exponential decay curve determined only by T2{T}_{2}T2​. The feature of the results obtained by the present method is similar to that obtained by the conventional coherent transient spectroscopy with short pulses, such as the photon echo. The time resolution in the present method, however, is limited only by ${\ensuremath{\tau}}_{c}$ much shorter than the light duration. By regarding the incoherent light as a series of random ultrashort pulses, the present four-wave-mixing process is also interpreted as the ensemble of numerous transient four-wave-mixing processes caused by various combinations of these pulses.
The effect of cross relaxation on the third-order nonlinear susceptibility, χ(3) (−ω2, ω1, −ω1, ω2), describing polarization spectroscopy experiments is calculated with a density matrix formalism. By using a model of inhomogeneously broadened two-level systems with a reservoir state and allowing for cross relaxation within the inhomogeneous line, we find that both the ratio of the maximum signal at ω1 = ω2 to the background and the broad component resembling the absorption band depend on the cross-relaxation rate. Also, one additional component with a characteristic width of the order of the spectral-diffusion rate Γ3 is expected to appear, depending on the value of this parameter. Furthermore, we estimate from published data [ Phys. Rev. A17, 1439 ( 1978)] the product of the transverse-relaxation time times the cross-relaxation time T2T3 to be 0.014 psec2 for cyanine dye and 0.0009 psec2 for malachite green oxalate.
The dependence of the Rayleigh-type optical mixing signal intensity on the incident pump and probe frequencies for different values of T1/T2 is shown in a three-dimensional plot for a homogeneously broadened line. The symmetry properties of the signal in this space and of the nonlinear process that generates the line are related. These properties are used to show the dependence of the measured spectra on the way in which the frequencies of the incident fields are varied. Furthermore, this plot in frequency space yields information that may be used for the determination of the relaxation times T1 and T2.
A nonperturbative analysis (in one of the fields) of the Rayleigh-type optical-mixing signal in an absorbing medium shows that it is more sensible to saturation than the effect that could be expected from ``absorption saturation arguments.'' We also report the observation of such high-order effects in the organic dye malachite green. We have found that an effective two-level system model with a longitudinal relaxation time of 1.1\ifmmode\pm\else\textpm\fi{}0.2 ps, a transverse relaxation time of 0.13\ifmmode\pm\else\textpm\fi{}0.05 ps, and a transition moment of 1.2 D account for the deviation from the third-order regime. However, the frequency region of the data that follows the predicted spectral deformation is power dependent and it shrinks as power increases.