Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

Journal of the Optical Society of America B

FEMTOSECOND QUANTUM BEATS IN OPTICAL TRANSMISSION-CORRELATION AND PUMP-PROBE MEASUREMENTS.

Masaharu Mitsunaga, Carson L. Tang

Published Jan 1, 1987• 0 citations
OpenAlex

Abstract

Recent femtosecond transmission-correlation measurements1 of large organic dye molecules revealed surprising details concerning the ultrafast relaxation dynamics of such dyes. Superposed on simple exponential decays, the observation of damped sinusoidal oscillations with a period of ~ 150 fs has been puzzling. We theoretically and numerically demonstrate that such oscillatory behavior could be due to quantum beats of closely spaced two levels, whose coherent superposition state is optically prepared and monitored by a pair of femtosecond pulses. Although studies of quantum beats have been developed in both fluorescence-type2 and nonfluorescence-type measurements, such as those based on photon echoes3 or polarization spectroscopy,4 this simple method gives a new approach to femtosecond time domain spectroscopy. The generalized perturbation theory5 of optical coherent transients is extended to the case of optical transmission-correlation or pump-probe-type experiments. The model used is a three-level system which has split levels in either the ground or optically excited states. Especially, if the ground state has sublevels, the system becomes quite similar to the case of coherent Raman beats. Both cases are shown to give quantum beats when the excitation pulses are short compared with the inverse sublevel splitting. The period and decay time of the damped sinusoid represent the separation energy and the dephasing time between the sublevels, respectively. Using third-order perturbation theory, the transmission-correlation signal STC(τ) as a function of the first-to-second pulse delay time Is derived for arbitrary-shaped excitation pulses and is given in the form of fourfold integrals with many terms.

Related papers

Theory of quantum beats in optical transmission-correlation and pump-probe measurements

Masaharu Mitsunaga, Carson L. Tang

A full density-matrix theory for quantum beats in optical transmission-correlation or pump-probe type of experiments is developed. The model used is a three-level system with split excited-state levels. It is demonstrated on the basis of perturbation theory that quantum beats should be observable in such experiments. Theoretical and numerical results are compared with the complex details, including damped sinusoidal decays, observed in recent femtosecond relaxation studies of large organic dye molecules. It is also shown that there is no separately identifiable decay component corresponding to any homogeneous or inhomogeneous optical dephasing time in such experiments. Similar beating should also be observable in ultrafast spectroscopy using incoherent light and in Raman-type energy-level configurations where the ground state contains split levels.

Physical Review A•Feb 1, 1987•94 citations

Theory of quantum beats in optical transmission-correlation and pump-probe experiments for a general Raman configuration

Ian A. Walmsley, Masaharu Mitsunaga, Carson L. Tang

A perturbative density-matrix theory of quantum beats developed previously has been extended to include the case of a three-level system with ground-state splitting. It is shown that quantum beats should be observable in a transmission-correlation experiment when the optical pulses are resonant or nonresonant with the excited state. The beats may be of magnitude comparable to those from a split excited state, and are insensitive to the amount of homogeneous or inhomogeneous broadening of the optical transitions.

Physical Review A•Nov 1, 1988•95 citations

Coherence from fluorescence correlations: Oscillatory femtosecond fluorescence in pentacene/p-terphenyl

Andreas Tortschanoff, Klemens Brunner, Ch. Warmuth +1 more

Spontaneous fluorescence has been used to measure the coherent femtosecond response of the organic, binary crystal pentacene/p-terphenyl. By using two-pulse excitation with phase-randomized pulses in an interferometric setup and analyzing the variance of the fluctuating intensity of correlated fluorescence photons, femtosecond beatings have been observed. The pattern of these terahertz oscillations is strongly dependent on the detuning frequency range of the exciting pulses, but is rather invariant with regard to the spectral position of the fluorescence probe window. In the interferometric regime of freely propagating pulses novel, ultrafast fluorescence carrier-wave oscillations superimposed to the beat structure have been obtained. The oscillatory signals evolve from a coherent superposition of optical free induction decays, caused by the different electronic transition energies of the pentacene absorber sites O1, O2, O3, and O4, respectively, are monitored as intrinsic, heterodyne beats by the fluorescence square detector. The major part of oscillations is thus considered to result from typical polarization interferences, but vibrational quantum beats are also extractable from the interferogram in the ultimate frequency regime of the pentacene S0→S1ν=1, S0→S1ν=2 resonances. The early picosecond-decay of the fluorescence beats reveals the mechanism of the loss of coherence to be mainly controlled by inhomogeneous dephasing at low phonon temperatures. A model of uncoupled two-level systems that includes Gaussian inhomogeneous broadening of the individual absorber sites and a Gaussian frequency distribution for the excitation pulses can account for the experimental data, quite adequately.

The Journal of Chemical Physics•Mar 1, 1999•19 citations

Phase-resolved time-domain nonlinear optical signals

Sarah M. Gallagher Faeder, David M. Jonas

A systematic theoretical and computational investigation of the microscopic factors which determine the phase of the signal field in time-resolved quasidegenerate three-pulse scattering experiments is presented. The third-order phase-matched response is obtained by density-matrix perturbation theory using a Green-function formalism for a system composed of two well-separated sets of closely spaced energy levels. Equations for calculating the electric field of four-wave-mixing signals generated by path-length delayed pulses are given. It is found that the phase of the signal field is determined by the excitation pulse phases, the dynamics of the nonlinear polarization decay, the product of four transition dipole matrix elements, and by a pulse-delay-dependent phase modulation at the frequency of the first dipole oscillation in the four-wave-mixing process. Analytic results for a two-level Bloch model show the phase shift from rapid nonlinear polarization decay. The product of dipole matrix elements is real and positive for three-level processes (bleached ground-state absorption and excited-state emission), but can be real and negative for some four-level Raman processes. The pulse-delay-dependent phase modulation treated here is closely related to the interferometric pulse-delay-dependent amplitude modulation observed in some collinear experiments, and plays a role in producing photon echos in inhomogeneously broadened samples. Numerical calculations of phase-resolved electric fields for finite duration pulses using a Brownian oscillator model appropriate for condensed-phase dynamics are presented. The ability of pulse-delay-dependent phase modulation to encode the frequency of the initially excited dipole onto the phase of the signal field can be exploited to examine energy-level connectivity, reveal correlations hidden under the inhomogeneous lineshape, and probe relaxation pathways in multilevel systems.

Physical Review A•Aug 18, 2000•41 citations

Excitation-Induced Phase Shifts of Heavy and Light Hole Quantum Beats in Multiple Quantum Wells

Wei E. I. Sha, A. E. Paul, Shekhar Patkar +1 more

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.

International Conference on Ultrafast Phenomena•Jan 1, 1994•0 citations

Heavy-hole–light-hole quantum beats in nonlinear transmission spectroscopy

Kai Wundke, U. Neukirch, J. Gutowski +1 more

The complex polarization behavior of quantum beating between heavy- and light-hole excitons in nonlinear pump-and-probe spectroscopy is experimentally investigated. The strain-split free excitons in thin high-quality ZnSe layers embedded in ternary ${\mathrm{ZnS}}_{\mathit{x}}$${\mathrm{Se}}_{1\mathrm{\ensuremath{-}}\mathit{x}}$ barriers served as the three-level system involved. Spectrally integrated pump-and-probe experiments confirm the theoretically predicted dependence of the quantum-beat phase on the relative polarization of the exciting fields. These observations are discussed in comparison with results from four-wave mixing obtained when using the same experimental setup. Beyond that, spectrally resolved transients measured on the light-hole resonance exhibit pronounced, weakly damped beating phenomena even at negative delay, i.e., with the probe pulses preceding the pump pulses. Additionally, for cross-polarized beams the quantum-beat phase is strongly dependent on the energy of detection. It turns out that the phase observed in the spectrally integrated mode is determined by the off-resonant contributions. \textcopyright{} 1996 The American Physical Society.

Physical review. B, Condensed matter•Apr 15, 1996•10 citations
Recent femtosecond transmission-correlation measurements1 of large organic dye molecules revealed surprising details concerning the ultrafast relaxation dynamics of such dyes. Superposed on simple exponential decays, the observation of damped sinusoidal oscillations with a period of ~ 150 fs has been puzzling. We theoretically and numerically demonstrate that such oscillatory behavior could be due to quantum beats of closely spaced two levels, whose coherent superposition state is optically prepared and monitored by a pair of femtosecond pulses. Although studies of quantum beats have been developed in both fluorescence-type2 and nonfluorescence-type measurements, such as those based on photon echoes3 or polarization spectroscopy,4 this simple method gives a new approach to femtosecond time domain spectroscopy. The generalized perturbation theory5 of optical coherent transients is extended to the case of optical transmission-correlation or pump-probe-type experiments. The model used is a three-level system which has split levels in either the ground or optically excited states. Especially, if the ground state has sublevels, the system becomes quite similar to the case of coherent Raman beats. Both cases are shown to give quantum beats when the excitation pulses are short compared with the inverse sublevel splitting. The period and decay time of the damped sinusoid represent the separation energy and the dephasing time between the sublevels, respectively. Using third-order perturbation theory, the transmission-correlation signal STC(τ) as a function of the first-to-second pulse delay time Is derived for arbitrary-shaped excitation pulses and is given in the form of fourfold integrals with many terms.
A full density-matrix theory for quantum beats in optical transmission-correlation or pump-probe type of experiments is developed. The model used is a three-level system with split excited-state levels. It is demonstrated on the basis of perturbation theory that quantum beats should be observable in such experiments. Theoretical and numerical results are compared with the complex details, including damped sinusoidal decays, observed in recent femtosecond relaxation studies of large organic dye molecules. It is also shown that there is no separately identifiable decay component corresponding to any homogeneous or inhomogeneous optical dephasing time in such experiments. Similar beating should also be observable in ultrafast spectroscopy using incoherent light and in Raman-type energy-level configurations where the ground state contains split levels.
A perturbative density-matrix theory of quantum beats developed previously has been extended to include the case of a three-level system with ground-state splitting. It is shown that quantum beats should be observable in a transmission-correlation experiment when the optical pulses are resonant or nonresonant with the excited state. The beats may be of magnitude comparable to those from a split excited state, and are insensitive to the amount of homogeneous or inhomogeneous broadening of the optical transitions.
Spontaneous fluorescence has been used to measure the coherent femtosecond response of the organic, binary crystal pentacene/p-terphenyl. By using two-pulse excitation with phase-randomized pulses in an interferometric setup and analyzing the variance of the fluctuating intensity of correlated fluorescence photons, femtosecond beatings have been observed. The pattern of these terahertz oscillations is strongly dependent on the detuning frequency range of the exciting pulses, but is rather invariant with regard to the spectral position of the fluorescence probe window. In the interferometric regime of freely propagating pulses novel, ultrafast fluorescence carrier-wave oscillations superimposed to the beat structure have been obtained. The oscillatory signals evolve from a coherent superposition of optical free induction decays, caused by the different electronic transition energies of the pentacene absorber sites O1, O2, O3, and O4, respectively, are monitored as intrinsic, heterodyne beats by the fluorescence square detector. The major part of oscillations is thus considered to result from typical polarization interferences, but vibrational quantum beats are also extractable from the interferogram in the ultimate frequency regime of the pentacene S0→S1ν=1, S0→S1ν=2 resonances. The early picosecond-decay of the fluorescence beats reveals the mechanism of the loss of coherence to be mainly controlled by inhomogeneous dephasing at low phonon temperatures. A model of uncoupled two-level systems that includes Gaussian inhomogeneous broadening of the individual absorber sites and a Gaussian frequency distribution for the excitation pulses can account for the experimental data, quite adequately.
A systematic theoretical and computational investigation of the microscopic factors which determine the phase of the signal field in time-resolved quasidegenerate three-pulse scattering experiments is presented. The third-order phase-matched response is obtained by density-matrix perturbation theory using a Green-function formalism for a system composed of two well-separated sets of closely spaced energy levels. Equations for calculating the electric field of four-wave-mixing signals generated by path-length delayed pulses are given. It is found that the phase of the signal field is determined by the excitation pulse phases, the dynamics of the nonlinear polarization decay, the product of four transition dipole matrix elements, and by a pulse-delay-dependent phase modulation at the frequency of the first dipole oscillation in the four-wave-mixing process. Analytic results for a two-level Bloch model show the phase shift from rapid nonlinear polarization decay. The product of dipole matrix elements is real and positive for three-level processes (bleached ground-state absorption and excited-state emission), but can be real and negative for some four-level Raman processes. The pulse-delay-dependent phase modulation treated here is closely related to the interferometric pulse-delay-dependent amplitude modulation observed in some collinear experiments, and plays a role in producing photon echos in inhomogeneously broadened samples. Numerical calculations of phase-resolved electric fields for finite duration pulses using a Brownian oscillator model appropriate for condensed-phase dynamics are presented. The ability of pulse-delay-dependent phase modulation to encode the frequency of the initially excited dipole onto the phase of the signal field can be exploited to examine energy-level connectivity, reveal correlations hidden under the inhomogeneous lineshape, and probe relaxation pathways in multilevel systems.
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.
The complex polarization behavior of quantum beating between heavy- and light-hole excitons in nonlinear pump-and-probe spectroscopy is experimentally investigated. The strain-split free excitons in thin high-quality ZnSe layers embedded in ternary ZnSx{\mathrm{ZnS}}_{\mathit{x}}ZnSx​${\mathrm{Se}}_{1\mathrm{\ensuremath{-}}\mathit{x}}$ barriers served as the three-level system involved. Spectrally integrated pump-and-probe experiments confirm the theoretically predicted dependence of the quantum-beat phase on the relative polarization of the exciting fields. These observations are discussed in comparison with results from four-wave mixing obtained when using the same experimental setup. Beyond that, spectrally resolved transients measured on the light-hole resonance exhibit pronounced, weakly damped beating phenomena even at negative delay, i.e., with the probe pulses preceding the pump pulses. Additionally, for cross-polarized beams the quantum-beat phase is strongly dependent on the energy of detection. It turns out that the phase observed in the spectrally integrated mode is determined by the off-resonant contributions. \textcopyright{} 1996 The American Physical Society.