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Physical Review A

Stochastic theory of time-resolved four-wave mixing in interacting media

Stefan Schmitt-Rink, Shaul Mukamel, Karl Leo, Jagdeep Shah, D. S. Chemla

Published Aug 1, 1991• 77 citations
Publisher

Abstract

We study the temporal profile of the time-resolved four-wave-mixing signal in media with strong polarization interactions, assuming a stochastic modulation of the optical-transition frequency. The model is exactly solvable and interpolates smoothly between Lorentzian (fast modulation) and Gaussian (slow modulation) broadening. We show that recently predicted and observed four-wave-mixing signals persist even in the latter limit, albeit with a different temporal profile.

DOI
10.1103/physreva.44.2124

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We study the temporal profile of the time-resolved four-wave-mixing signal in media with strong polarization interactions, assuming a stochastic modulation of the optical-transition frequency. The model is exactly solvable and interpolates smoothly between Lorentzian (fast modulation) and Gaussian (slow modulation) broadening. We show that recently predicted and observed four-wave-mixing signals persist even in the latter limit, albeit with a different temporal profile.
The optical density of a resonant medium significantly affects the output signal in time resolved nonlinear optical interactions. The resonant interaction with a medium reshapes any propagating short pulse, and the mutual interaction of several such pulses, as in four-wave mixing, must be treated self-consistently. We present a theoretical framework for the proper handling of the propagation of all pulses, input as well as generated, in the small area limit. For optically thick resonant absorbers, negative time delay signals are observed, and the apparent decay rate of the induced polarization is faster than the rate observed for thin samples. We experimentally measure degenerate four-wave mixing in an atomic medium as an example, and demonstrate the quality of the theoretical model by the excellent fit to measured signals over several orders of magnitude. The improved understanding enables us to provide a simple, but surprisingly accurate, estimate for the apparent decay rate in homogeneously broadened optically thick media: If the absorption is given by \ensuremath{\alpha}, the propagation length is L, and the transverse relaxation time is T2{\mathit{T}}_{2}T2​, the apparent decay rate 2/Ta{\mathit{T}}_{\mathit{a}}Ta​ of a time resolved four-wave mixing signal is given by 2/Ta{\mathit{T}}_{\mathit{a}}Ta​=(2/T2{\mathit{T}}_{2}T2​)(1+\ensuremath{\alpha}L/2).
Four-wave mixing in homogeneously broadened, two-level atoms, driven by time-delayed, correlated phase-diffusing optical fields is investigated. The spectrum of the driving field has an arbitrary bandwidth, i.e., it can have a Lorentzian or a Gaussian profile or an intermediate profile (Voigt). A time delay between the strong pump and weak probe field provides a partial correlation between the fields, and this time delay makes the composite field seen by the atoms non-Markovian. It is shown that the calculation of the four-wave-mixing signal reduces to the solution of six coupled Langevin equations with multiplicative noise; Monte Carlo techniques are utilized to study the response of the atoms to non-Markovian fields. A technique for numerically simulating phase-diffusing fields with colored frequency fluctuations is shown. The four-wave-mixing profiles are found to be significantly different from those for which the driving field is chaotic. The profiles show oscillatory behavior as evidence of the Rabi frequency, a feature not seen in previous works. For some parameter values, a revival of the signal is seen for an increasing time delay, analogous to the revivals seen in chaotic field signals [Phys. Rev. A 44, 6009 (1991)].
Time-resolved four-wave-mixing experiments are usually interpreted in terms of noninteracting two-level systems in order to obtain information on the polarization dephasing time T2{\mathit{T}}_{2}T2​. Recent experiments involving excitonic resonances in semiconductor quantum wells (including results presented in this paper) show striking qualitative deviations from this simple picture. In particular, an exponential tail is observed at low excitation for negative time delays. At high excitation, the four-wave-mixing signal is found to evolve into two distinct temporal maxima. We demonstrate that the microscopic origin of this time dependence can be understood in terms of coherent exciton-exciton interactions. We show in fact that this behavior is more general and should be seen in numerous dense media where strong nonlinear interactions of polarizations occur. In addition to presenting rigorous numerical results, we analyze two simple situations in which such interactions exist: dielectric media with local-field effects and the anharmonic oscillator. We derive analytical expressions for their time-dependent four-wave-mixing response and discuss the physical origin of these new nonlinear-optical effects.
In this study, we extended the observation of the effect of the coherence of a laser field to four-wave mixing interactions in atomic media. These measurements will help us understand quantitatively recent techniques employing broad-band nanosecond laser pulses for measurements of sub-picosecond dipole relaxation lifetimes in a variety of media. The coherence of the laser field in this work is controlled using random phase/frequency modulation techniques, creating a field in the laboratory known as the phase diffusion field. The four-wave mixing signal is generated by an ensemble of two-level atoms (Na) interacting with degenerate broad-band, correlated, pump and probe fields. This two-level system is produced by optically pumping the sodium atoms into a single hyperfine component of the ground state. Data sets were taken without and with noise applied to the optical field. For the latter, we measured the dependence of the power of the four-wave mixing signal on the delay times between the pump and probe beams. These data sets were compared with the computer simulation results.
We show that four-wave mixing in optically dense media is very different than in an optically thin medium. In time-resolved degenerate four-wave mixing we experimentally observe ``negative'' time delay response, fast decay rates at short delay times, and broad shoulders at long delays. The observations are explained very well in terms of pulse propagation effects, and a theoretical framework is presented for the analysis of the nonlinear interaction. We treat both the incident and generated fields self-consistently, and solve for the interaction of short pulses with a resonantly absorbing medium. The implications for the extraction of relaxation rates from four-wave-mixing experiments involving ultrashort pulses in optically dense matter are discussed.