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

High Power Laser and Particle Beams

DIFFERENTIAL-PHASE SPECTROSCOPY FOR COHERENT CARRIERS WITH LASER FEMTOSECOND PULSE PAIRS

Yun Fang

Published Jan 1, 2000• 0 citations
OpenAlex

Abstract

It is proved that both amplitude and phase in instantaneous optical processes can be detected from the number density of the excited state populations of coherent carriers when excited with femtosecond laser pulse pairs. Experimental technique of phase spectroscopy is used for investigations of semiconductor GaAs and rare earth solids. Phase spectra of GaAs, crystal Nd:YVO 4 and powdered Nd:YAG are obtained. Dephasing time of GaAs exciton is 190fs at 77K and the Nd:YVO 4 and Nd:YAG are 300fs at room temperature.

Related papers

Ultrafast phase dynamics of coherent carriers in GaAs

Xiangyang Yu, Qi Luo, Wen‐lan Li +3 more

Ultrafast phase dynamics of free-induction decay for carriers in bulk GaAs is studied with differential-phase spectroscopy. The instantaneous phase shifts of the free-induction decay with respect to the excitation pulses are extracted from simultaneously recorded laser pulse autocorrelation and free-induction decay in GaAs. Ultrafast phase dynamics during and immediately after the femtosecond pulse excitation are numerically evaluated with optical Bloch equations using pump pulse and semiconductor exciton parameters as input. Good agreement of the theory with experiment is obtained.

Applied Physics Letters•Dec 7, 1998•13 citations

Theory and experiment of coherent wave packet dynamics in rare earth solids: Absorption spectrum vs femtosecond fringe-resolved interferogram

Qi Luo, D. C. Dai, G. Q. Wang +5 more

Coherent dynamic property of neodymium yttrium aluminum garnet (Nd:YAG) crystal at 77 K is studied via the conventional absorption, the femtosecond fringe-resolved wave packet interferometry, and the related difference-phase spectrum. The recorded interferogram exhibits beatings in subpicosecond time scale arising from the interferences among various weakly split 4f-electronic states and the coupled vibronic optical phonon sidebands. The electron–phonon coupling in Nd:YAG can be well described by multiple Brownian oscillators model involving in each individual electronic transition. The parameters for characterizing material coherence and relaxation are determined via the theoretical modelings of both the frequency and the time-domain experimental signals.

The Journal of Chemical Physics•Jan 22, 2001•8 citations

Quantum Coherence in Ultrafast Semiconductor Spectroscopy

H. Haug

Coherent optical phenomena such as the optical Stark effect, Rabi flopping, photon echo and quantum beating which are well-known in atomic spectroscopy can also be observed in semiconductors by using femtosecond laser pulses. On these short time scales, the quantum coherence of the optical excitations in the solid do not only influence the optical properties but change at the same time the relaxation and dephasing kinetics. The quasi-classical Boltzmann kinetics has to be replaced by quantum kinetics. Coherence leads to the appearance of memory in the scattering integrals. For femtosecond four-wave mixing and pump-and-probe spectroscopy the use of quantum kinetics for LO-phonon and for carrier-carrier scattering will be reviewed.

Journal of Nonlinear Optical Physics & Materials•Jun 1, 1998•1 citation

Resonant Secondary Emission from Two-Dimensional Excitons: Femtosecond Time Evolution of the Coherence Properties

Michael Woerner, Jagdeep Shah

Using a novel technique, we simultaneously study the femtosecond dynamics of the amplitude and the coherence of resonant secondary emission from GaAs quantum wells. Two phase-locked pulses resonantly excite excitons in the semiconductor and the subsequently emitted radiation is detected by femtosecond up-conversion. In experiments at various delays and phases between the excitation pulses we identify three different contributions to the secondary emission with different coherence properties in time.

Physical Review Letters•Nov 9, 1998•71 citations

Coherent optical polarization of bulk GaAs studied by femtosecond photon-echo spectroscopy

A. Lohner, Kai Rick, P. Leisching +5 more

The nonlinear polarization close to the band gap of GaAs is studied by spectrally and temporally resolved four-wave mixing. Excitonic and free carrier contributions both excited within the bandwidth of the 100 fs pulses are distinguished for the first time. The excitonic part dominates at carrier densities below ${10}^{16}$ ${\mathrm{cm}}^{\mathrm{\ensuremath{-}}3}$. At higher density, nonthermalized free carriers give rise to an additional component resonant to the pulse that shows a photon-echo-like time behavior. Monte Carlo simulations including the coherent polarization and the scattering dynamics of the carriers account for the data.

Physical Review Letters•Jul 5, 1993•80 citations

Coherent optical spectroscopy of promising materials for solid-state optical processors

В. В. Самарцев

State of the art of optical coherent spectroscopy of doped solids that are promising as information carriers for optical processors is reviewed. Special attention is paid to optical echo spectroscopy of doped crystals classified as the Van-Vleck paramagnets where the long-lived stimulated echo is observed with the optical-memory time reaching several hours at low temperatures. Modern elaborations of optical echo processors based on this echo phenomenon are discussed. Physical principles of femtosecond echo spectroscopy and coherent four-wave mixing spectroscopy are formulated. The abilities of these methods in the diagnostics of fast processes at room temperature are illustrated using examples of a doped polymer films. The results of elaborations of a new branch of optical spectroscopy (biphoton spectroscopy) are also presented. The advantages and possible applications of this method are demonstrated using an example of two crystals (Er 3+ :YAG and Cr 3+ :Al 2 O 3 ).

Laser Physics•Feb 1, 2010•19 citations
It is proved that both amplitude and phase in instantaneous optical processes can be detected from the number density of the excited state populations of coherent carriers when excited with femtosecond laser pulse pairs. Experimental technique of phase spectroscopy is used for investigations of semiconductor GaAs and rare earth solids. Phase spectra of GaAs, crystal Nd:YVO 4 and powdered Nd:YAG are obtained. Dephasing time of GaAs exciton is 190fs at 77K and the Nd:YVO 4 and Nd:YAG are 300fs at room temperature.
Ultrafast phase dynamics of free-induction decay for carriers in bulk GaAs is studied with differential-phase spectroscopy. The instantaneous phase shifts of the free-induction decay with respect to the excitation pulses are extracted from simultaneously recorded laser pulse autocorrelation and free-induction decay in GaAs. Ultrafast phase dynamics during and immediately after the femtosecond pulse excitation are numerically evaluated with optical Bloch equations using pump pulse and semiconductor exciton parameters as input. Good agreement of the theory with experiment is obtained.
Coherent dynamic property of neodymium yttrium aluminum garnet (Nd:YAG) crystal at 77 K is studied via the conventional absorption, the femtosecond fringe-resolved wave packet interferometry, and the related difference-phase spectrum. The recorded interferogram exhibits beatings in subpicosecond time scale arising from the interferences among various weakly split 4f-electronic states and the coupled vibronic optical phonon sidebands. The electron–phonon coupling in Nd:YAG can be well described by multiple Brownian oscillators model involving in each individual electronic transition. The parameters for characterizing material coherence and relaxation are determined via the theoretical modelings of both the frequency and the time-domain experimental signals.
Coherent optical phenomena such as the optical Stark effect, Rabi flopping, photon echo and quantum beating which are well-known in atomic spectroscopy can also be observed in semiconductors by using femtosecond laser pulses. On these short time scales, the quantum coherence of the optical excitations in the solid do not only influence the optical properties but change at the same time the relaxation and dephasing kinetics. The quasi-classical Boltzmann kinetics has to be replaced by quantum kinetics. Coherence leads to the appearance of memory in the scattering integrals. For femtosecond four-wave mixing and pump-and-probe spectroscopy the use of quantum kinetics for LO-phonon and for carrier-carrier scattering will be reviewed.
Using a novel technique, we simultaneously study the femtosecond dynamics of the amplitude and the coherence of resonant secondary emission from GaAs quantum wells. Two phase-locked pulses resonantly excite excitons in the semiconductor and the subsequently emitted radiation is detected by femtosecond up-conversion. In experiments at various delays and phases between the excitation pulses we identify three different contributions to the secondary emission with different coherence properties in time.
The nonlinear polarization close to the band gap of GaAs is studied by spectrally and temporally resolved four-wave mixing. Excitonic and free carrier contributions both excited within the bandwidth of the 100 fs pulses are distinguished for the first time. The excitonic part dominates at carrier densities below 1016{10}^{16}1016 ${\mathrm{cm}}^{\mathrm{\ensuremath{-}}3}$. At higher density, nonthermalized free carriers give rise to an additional component resonant to the pulse that shows a photon-echo-like time behavior. Monte Carlo simulations including the coherent polarization and the scattering dynamics of the carriers account for the data.
State of the art of optical coherent spectroscopy of doped solids that are promising as information carriers for optical processors is reviewed. Special attention is paid to optical echo spectroscopy of doped crystals classified as the Van-Vleck paramagnets where the long-lived stimulated echo is observed with the optical-memory time reaching several hours at low temperatures. Modern elaborations of optical echo processors based on this echo phenomenon are discussed. Physical principles of femtosecond echo spectroscopy and coherent four-wave mixing spectroscopy are formulated. The abilities of these methods in the diagnostics of fast processes at room temperature are illustrated using examples of a doped polymer films. The results of elaborations of a new branch of optical spectroscopy (biphoton spectroscopy) are also presented. The advantages and possible applications of this method are demonstrated using an example of two crystals (Er 3+ :YAG and Cr 3+ :Al 2 O 3 ).