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Advances in multi-photon processes and spectroscopy

WHAT ROLE CAN FOUR-WAVE MIXING TECHNIQUES PLAY IN COHERENT CONTROL?

Vadim V. Lozovoy, Emily J. Brown, Igor Pastirk, Bruna Irene Grimberg, Marcos M. Dantus

Published Dec 1, 2000• 3 citations
Publisher

Abstract

The role of four-wave mixing (FWM) techniques in coherent control is considered from the point of view of some of the most important developments in this field over the past years, namely multiphoton excitation, pump-dump methods, interference between coherent pulses, chirped laser pulses, and optimal control. FWM techniques provide a powerful platform for combining coherently multiple laser pulses. We explore the effectiveness of these techniques in controlling chemical reactions. The phase relationship between the pulses is maintained by detecting the signal in a phase-matching direction. The results presented show control over the observed dynamics from ground and excited state populations. The FWM signal results from the polarization of the sample following three different electric field interactions. The virtual echo sequence is achieved by the interactions of the sample with three consecutive electric fields characterized by exp[i(kx-w t)], exp[-i(kx-w t)] and exp[i(kx-w t)]. This sequence allows control over the observed ground or excited state dynamics. With the photon echo pulse sequence, characterized by interactions with exp[-i(kx-w t)], exp[i(kx-w t)], and exp[i(kx-w t)], we find that control of ground and excited state populations is not achieved.

DOI
10.1142/9789812791948_0005

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The role of four-wave mixing (FWM) techniques in coherent control is considered from the point of view of some of the most important developments in this field over the past years, namely multiphoton excitation, pump-dump methods, interference between coherent pulses, chirped laser pulses, and optimal control. FWM techniques provide a powerful platform for combining coherently multiple laser pulses. We explore the effectiveness of these techniques in controlling chemical reactions. The phase relationship between the pulses is maintained by detecting the signal in a phase-matching direction. The results presented show control over the observed dynamics from ground and excited state populations. The FWM signal results from the polarization of the sample following three different electric field interactions. The virtual echo sequence is achieved by the interactions of the sample with three consecutive electric fields characterized by exp[i(kx-w t)], exp[-i(kx-w t)] and exp[i(kx-w t)]. This sequence allows control over the observed ground or excited state dynamics. With the photon echo pulse sequence, characterized by interactions with exp[-i(kx-w t)], exp[i(kx-w t)], and exp[i(kx-w t)], we find that control of ground and excited state populations is not achieved.
Three-pulse four-wave mixing (FWM) is used here to study and control laser excitation processes. For general laser excitation processes, after a molecule interacts resonantly with a laser pulse, the molecule has a probability of being in the ground or in the excited state. Control over this process depends on the phase and amplitude of the electric fields that interact with the molecular system. Here we show how three-pulse FWM can be used to control the excitation of iodine molecules. Depending on the time delay between the first two pulses, the observed signal reflects the dynamics of the ground or excited state. A theoretical formalism based on the density matrix formulation is presented and solved for a four-level system. Experiments are found to be in excellent agreement with the theory. The influence of linear chirp on three-pulse FWM experiments is explored. Spectrally dispersed three-pulse FWM is found to be extremely useful for studying the effect of chirp on laser excitation of molecular systems. Experimental demonstrations of these effects are included.
Control of coherence and population transfer between the ground and excited states is reported using three-pulse four-wave mixing. The inherent vibrational dynamics of the system are utilized in timing the pulse sequence that controls the excitation process. A slight alteration in the pulse sequence timing causes a change in the observed signal from coherent vibration in the ground state to coherent vibration in the excited state. This control is demonstrated experimentally for molecular iodine. The theoretical basis for these experiments is discussed in terms of the density matrix for a multilevel system.
Summary form only given. The developments with coherent control (CC) techniques in optical spectroscopy have recently demonstrated population control and coherence manipulations when the induced optical phase is explored with phase-locked laser pulses. These and other developments have been guiding the new research field of quantum control including the recent applications to semiconductors and nanostructures. We study the influence of inhomogeneous broadening in semiconductors on CC results. Photoluminescence (PL) and the coherent emission in four-wave mixing (FWM) is recorded after resonant excitation with phase-locked laser pulses. The sample is a narrow GaAs single quantum well.
The four-wave mixing produced with two ultrashort phase-locked !-3! laser pulses propagating coherently in a two-level system in the infrared spectral region is shown to depend on the pulses relative phase. The Maxwell-Bloch equations are solved beyond the rotating-wave approximation to account for field frequencies which are largely detuned from the atomic resonance. The relative phase dominating the efficiency of the coupling to the 5! anti-Stokes Raman component is determined by sign of the total ac Stark shift induced in the system, in such a way that the phase influence disappears precisely where the ac Stark effect due to both pulses is compensated. This fundamental quantum interference effect can be the basis for nonlinear ultrafast optical spectroscopy techniques. Phenomena arising from the coherent control of nonlinear interactions are of importance in fields as diverse as optoelectronics and materials research, in high harmonic generation, in photoionization or molecular dissociation, and in biological applications such as spectroscopy and imaging, among others [1, 2, 3, 4, 5, 6, 7]. Optical quantum coherent control is based on the fact that the phases of interfering transition amplitudes in light-matter interactions can be controlled through the optical phase of coherent light sources that drive the interaction, in such a way that the transition rates to final states and the dynamics at various stages of the process can be modified [1]. In a recent paper [8], a theoretical investigation on the quantum coherent control of the optical transient four-wave mixing of two intense phase-locked femtosecond laser pulses of central angular frequencies ω and 3ω propagating in a two-level atom (TLA) was reported. It was shown how the nonlinear (χ (3) ) coupling to the antiStokes Raman field at frequency 5ω depends critically on the initial relative phase φ of the propagating pulses. In Ref. [8], the study was centered to intense pulses in the visible and ultraviolet spectral regions, with frequencies at resonance or lower than the atomic transition. The phenomena observed in [8], however, can be scaled to various laser and material parameters. In the infrared spectral range, for instance, experiments on ultrafast molecular dynamics are frequently performed by help of twocolor pump probe nonlinear spectroscopy techniques. In this type of studies, due to the high intensities inherent to ultrashort (subpicosecond) pulses, nonlinear effects such as stimulated Raman processes may become important and are often utilized as a complementary tool to gain information [9]. In this Letter, we address the conditions for quantum coherent control of transient four-wave mixing interactions with two phase-locked ω-3ω femtosecond laser pulses in the mid-IR spectral region. Our purpose is to reveal the basic physics for a strict two-level medium and to this end the Maxwell-Bloch TLA will be considered. We will study pulses with a duration of 300 fs (with a w 5w
We demonstrate coherent control over interference between different Liouville-space pathways that describe the generation of the nonlinear optical polarization in a stimulated photon echo. This control was exercised by phase-locking of the excitation pulses and observed in the heterodyne detected echo signal. A theoretical analysis of the effect is presented and found to be in good agreement with the obtained results. The relation between this novel time-domain interference effect and the pressure-induced extra resonance in four-wave mixing spectroscopy is discussed.
By use of an optical coherent-control technique we demonstrate and analyze the control of transitions involved in the generation of four-wave-mixing signals in a semiconductor quantum well for the two different four-wave-mixing directions and for different sequences of the excitation pulses. Results are presented for frequency- as well as for time-resolved signals. A doubling of the coherent switching frequency is found which occurs if the laser pulses performing the control process contribute quadratically to the wave-mixing signal. A direct comparison between experiment and microscopic theory reveals how the coherent-control process acts on the coherent polarization of the exciton-biexciton system in all different configurations. An additional interpretation of the experimental results based on a simplified few-level model is able to provide an intuitive understanding of the relevant processes which govern the coherent control of the excitonic and biexcitonic wave-mixing polarizations.