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The Journal of Chemical Physics

Wigner spectrogram representations of heterodyne-detected four-wave-mixing and fluorescence up-conversion

Shaul Mukamel

Published Sep 15, 1997• 41 citations
Publisher

Abstract

Gated spontaneous emission and four-wave-mixing signals are expressed using a mixed time-frequency representation of the fields (Wigner spectrograms) and of the material response functions. Well-separated and overlapping pulses are described using two-sided (noncausal) and one-sided (causal) spectrograms, respectively. Pump–probe and fluorescence spectra are recast in an anologous form which facilitates the direct comparison of the underlying microscopic dynamics.

DOI
10.1063/1.474791

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Gated spontaneous emission and four-wave-mixing signals are expressed using a mixed time-frequency representation of the fields (Wigner spectrograms) and of the material response functions. Well-separated and overlapping pulses are described using two-sided (noncausal) and one-sided (causal) spectrograms, respectively. Pump–probe and fluorescence spectra are recast in an anologous form which facilitates the direct comparison of the underlying microscopic dynamics.
The use of phase-locked pulses in various spectroscopic techniques related to the third-order polarization P(3) is analyzed. Using correlation function expressions for the nonlinear response function, we clarify the interrelationship among several photon echo, pump–probe, and spontaneous light emission techniques, without alluding to any specific model for the material system. By combining phase-locked pulses and heterodyne detection it becomes possible to probe separately the real and imaginary parts of the nonlinear response function. Combining two phase-locked pulse excitation with time-resolved detection of the spontaneous light emission allows direct separation of the Raman and fluorescence contributions.
In this article, we analyse a new sensitive spectroscopic technique in which a sample cell is irradiated by a two-frequency pump beam (ω + Δ ± δ/2) and a counter-propagating probe beam (ω). The phase-conjugate fields re-emitted at frequencies ω ± δ, via four-wave mixing processes, are detected through their heterodyne beating with the probe field. The properties of the heterodyne beat signal are studied by means of a perturbation calculation of the nonlinear response of the medium, carried out to the third order in the incident fields. In resonant gas media, the emission lineshape exhibits a Doppler-free doublet structure [frequency splitting 3 δ/2 for single-photon resonances, and δ/2 for two-photon transitions]. By using a phase-sensitive detection of the beat signal, one can separately analyse real (dispersion) or imaginary parts (absorption) of the nonlinear susceptibility. For single-photon transitions, the signal phase shift is related to the atomic levels lifetime and allows one to study the relaxation dynamics in gas phase (like quenching collisions, velocity diffusion, etc...). This is particularly interesting for cross-over resonances, in which only the common level contributes. In three-level systems, one also predicts a selective resonant enhancement of the phase-conjugate emission through Raman-type two-photon processes. Most of these predictions have been experimentally verified.
The effect of overlapping pump and gate pulses on time- and frequency-gated spontaneous emission spectra is explored for a model of material dynamics that accounts for strong nonadiabatic and electron-vibrational coupling effects, vibrational relaxation, and optical dephasing, thus representing characteristic features of photoinduced excited-state dynamics in large molecules in the gas phase or in condensed phases. The behaviors of the sequential, coherent, and doorway-window contributions to the spontaneous emission spectrum are studied separately. The interrelation between the sequential and coherent contributions is demonstrated to be sensitive to the carrier frequencies of the pump and gate pulses and also to the optical dephasing rate, opening the possibility of an experimental determination of the latter. The coherent contribution is shown to dominate the spectrum at specific emission frequencies.
The theory of time- and frequency-gated (TFG) spontaneous emission (SE) spectra is elaborated. The present formulation generalizes previous derivations, clarifies the interrelations between different existing expressions, and establishes the validity of certain commonly assumed approximations. We obtain various explicit expressions for TFG SE spectra, which are suitable for performing actual calculations for nontrivial systems and which allow us to establish generic (that is, model-independent) properties of TFG spectra. The doorway-window picture of temporally and spectrally resolved spectra is further developed. It is shown that, to the leading order in the pump and probe pulses, the TFG SE signal is equivalent to the stimulated-emission contribution to the integral pump-probe spectrum in the case of nonoverlapping pulses. The theory is illustrated for the example of an electronic two-level system with a single Condon-active harmonic vibrational mode that is coupled to a thermal bath. The effect of imperfect time and frequency resolution is studied. It is pointed out that the TFG SE spectrum carries information not only on the strength of the system-bath coupling, but also on the relative magnitude of the bath correlation time.
Abstract This tutorial provides a joint theoretical and experimental overview of heterodyne wave mixing spectroscopy, focusing mainly on four-wave mixing (FWM). This powerful and versatile time-resolved nonlinear optical spectroscopy technique enables the investigation of individual localized single photon emitters, as well as microscopy of extended samples, e.g. two-dimensional transition metal dichalcogenides. Starting with the fundamental theory of optically driven two-level systems, we motivate the utility of wave mixing spectroscopy via a discussion on homogeneous and inhomogeneous linewidths which can be independently measured using FWM. We then provide a detailed overview of the heterodyne wave mixing setup operated by one of the authors (JK) at Institut Néel in Grenoble, supported by theoretical modeling of the signal detection process. Throughout the paper we elaborate on important benefits of heterodyne wave mixing spectroscopy, e.g. background-free detection, measurement of the full signal field including amplitude and phase, and investigation of coupling mechanisms in few-level systems. Within the context of the latter point we discuss the significance of two-dimensional FWM spectra. This tutorial is dedicated to students, young researchers, as well as experts in the field of nonlinear spectroscopy in general and FWM in particular. It explains the fundamental concepts and building blocks required to operate a heterodyne wave mixing experiment both from the experimental and theoretical side. This joint approach is helpful for theoreticians who want to accurately and quantitatively model wave mixing signals, as well as for experimentalists who aim to interpret their recorded data.