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Physical Review A

Quantum beats induced by spectral diffusion between independent two-level systems

Claudine Crépin

Published Jan 6, 2003• 11 citations
Publisher

Abstract

We analyze theoretically the time-resolved signal detected in three-pulse, photon echo experiments where several independent two-level systems are involved, in a case when the time delay T between the two last pulses is much longer than delay $\ensuremath{\tau}$ between the two first pulses. A spectral diffusion process on a long time scale is included in the calculation of the $\ensuremath{\tau}$-dependent response signal. If spectral diffusion occurs between the different systems, the signal exhibits quantum beats instead of the polarization interferences observed without spectral diffusion. This analysis provides different insights on dynamical processes and spectroscopy, as demonstrated in examples of experimental results obtained on vibrational dynamics of molecules embedded in matrices.

DOI
10.1103/physreva.67.013401

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International Conference on Ultrafast Phenomena•Jan 1, 1994•0 citations
We analyze theoretically the time-resolved signal detected in three-pulse, photon echo experiments where several independent two-level systems are involved, in a case when the time delay T between the two last pulses is much longer than delay \ensuremathτ\ensuremath{\tau}\ensuremathτ between the two first pulses. A spectral diffusion process on a long time scale is included in the calculation of the \ensuremathτ\ensuremath{\tau}\ensuremathτ-dependent response signal. If spectral diffusion occurs between the different systems, the signal exhibits quantum beats instead of the polarization interferences observed without spectral diffusion. This analysis provides different insights on dynamical processes and spectroscopy, as demonstrated in examples of experimental results obtained on vibrational dynamics of molecules embedded in matrices.
It is the purpose of the present paper to study the dynamics underlying a three-pulse photon-echo process performed on a vibronic system coupled to non-Markovian baths, when a neighboring level enters into the global dynamical evolution because of broadband excitation required in these experiments. Particular emphasis is on the energy gap between the vibronic levels, but also on the fluctuation amplitudes and correlation times of their corresponding thermal baths. The photon-echo signal appears to be very sensitive to the additional interfering contributions introduced by the neighboring vibronic level. It is shown that these contributions associated to the pathways involving different vibronic states are modulated by their corresponding energy gap. As a consequence, these contributions to the integrated photon-echo signal strongly decrease for large energy gaps. Also, an oscillating behavior is observed on the time dependence of the photon-echo signal resulting from the summation of the contributions provided by the individual vibronic levels. Moreover, the influence of the non-Markovian character of the baths, accountable for inhomogeneous broadening, affects the amplitude and the time dependence of the photon-echo signal, as well as its dependence with the delay time of the laser pulses. Of course, for longer times a Markovian dynamical evolution is recovered.
We analyze theoretically the quantum beat and the polarization interference phenomena observed as oscillations in pulsed four-wave mixing. We show that resolution of the signal with respect to the delay between the incoming pulses as well as the detection frequency provides valuable information on the nature of the oscillations. Most importantly, it is very simple to distinguish between polarization interference from two independent optical transitions and quantum beats from a three-level system. In case of polarization interference, the phase of the oscillations shifts \ensuremath{\pi} when the detected frequency passes any of the resonances. In case of quantum beat, the phase has little dependence on the detected frequency near the resonance.
The role of weakly chirped pulses (time bandwidth product, DeltanuDeltatau<0.61) on three-pulse photon echo signals has been systematically studied. Pulses with varying chirp were characterized with frequency resolved optical gating (FROG) and used to measure spectrally resolved three-pulse photon echoes of a dye in solution. The weakly chirped pulses give rise to markedly different echo signals for population times below approximately 100 fs. The chirped pulses can decrease or enhance spectral signatures of an excited state absorption transition in the echo signal. Furthermore, the observed dephasing dynamics depend on the phase of the electric fields. Simulations based on a three-level model and the electric fields retrieved from the FROG traces give a good agreement for photon echo experiments with both transform limited and chirped pulses. The simulations also allow for a numerical investigation of effects of chirp in two-dimensional spectroscopy. For a two-level system, the chirped pulses result in nonelliptical two-dimensional spectra that can erroneously be interpreted as spectral heterogeneity with frequency dependent dephasing dynamics. Furthermore, chirped pulses can give rise to "false" cross peaks when strong vibrational modes are involved in the system-bath interaction.
We show that time-resolved quantum beat spectroscopy in the four-wave mixing (FWM) geometry is a unique tool to investigate the electronic multi-level system associated with spectrally adjacent excitonic resonances. We have studied heavy- and light-hole excitons, excitons associated with different and spatially separated quantum wells, and excitons associated with spatially separated growth islands within the same quantum well. Though the linear spectra are qualitatively similar in all three cases, the respective beating of the time-resolved FWM-signal shows a very different dynamic behaviour in each case. We discuss appropriate electronic multi-level schemes and show that exciton transitions within different quantum wells can be described by independent twolevel systems. In contrast, excitonic transitions associated with different and spatially separated growth islands having different quantum well thickness are not independent but coupled.
In recent years, transient four-wave mixing (FWM) techniques have been used to investigate the dephasing times of non-equilibrium carriers in semiconductor heterostructures by monitoring the decay of the macroscopic polarization. Initially, this decay was measured by temporally-integrating the scattered FWM signal as a function of time delay between two (or more) pump pulses. More recently, the macroscopic polarization decay has been measured by time-resolving the FWM signal by cross correlating it with an ultrashort laser pulse via frequency up-conversion in a nonlinear crystal. When excitons with slightly different energies are excited, oscillations (or beats) have been observed both in the time-integrated FWM signal and in the time-resolved FWM signal. Such beats have been observed, for example, between light- and heavy-hole excitons and between excitons in wells of different widths. Both the spectral behavior1 of the time-integrated FWM signal and the temporal behavior2 of the time-resolved signal have been shown to allow the distinction between the polarization interference associated with two independent oscillators and the quantum beats associated with two coupled oscillators which share a common level. In addition, it has been demonstrated3 that the quantum beats produced by incident pulses with parallel polarizations are exactly out of phase (by π) with the beats produced by orthogonally polarized pulses. In each case1-3, the period and phase of the beats and the polarization of FWM signal were explained by using a six-level model, which excluded many-body effects, to describe the J=1/2 conduction and J=3/2 valence states. Within the last few months, however, it has been shown that a complete description of the polarization selection rules for the FWM signal requires excitation-induced dephasing4 or disorder-induced coupling of the σ + and σ – excitonic transitions5.