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

Springer eBooks

Resonant Scattering of Light by Molecules: Time-Dependent and Coherent Effects

Frank A. Novak, Joel M. Friedman, Robin M. Hochstrasser

Published Jan 1, 1978• 9 citations
Publisher
DOI
10.1007/978-1-4684-2352-5_5

Related papers

Effects of bath-induced vibrational transitions on time-resolved resonant light scattering from molecules in condensed phases

Yukiyoshi Ohtsuki, Yuichi Fujimura

Chemical Physics•Jun 1, 1989•3 citations

Intensity correlation function for a resonant weak light field scattered by a many-particle system. The bunched and antibunched components

A. A. Villaeys, Karl F. Freed

The authors present a weak light field, scattering theoretical description of the intensity autocorrelation function for the scattered light from a many-atom (molecule) system. The theory considers both resonant and near-resonant scattering for atoms with many sublevels in both the ground and electronically excited states, and it incorporates the effects of the finite coherence time of the incident radiation. The theory is derived using incident two-photon wave packets with spatial dispersion among the target atoms. Purely anti-bunching contributions arise from single-atom-two-photon scattering and from successive two-atom-two-photon scattering events. However, there are interleaved two-atom-two-photon scattering processes which provide purely bunching contributions since both atoms may be scattering at the same time. Path length differences in the successive two-atom scatterings can also induce some bunching character to the correlation function. The dependence of the risetime and decay of the intensity correlation function upon the atomic excited state lifetimes and the coherence time of the incident light emphasises the correlation between photons which have been coherently and/or incoherently scattered.

Journal of Physics B Atomic and Molecular Physics•Jul 28, 1980•2 citations

Theoretical aspects of the resonant scattering of light by molecules

Frank A. Novak

•Jan 1, 1977•1 citation

Coherent Stokes Raman scattering with incoherent light for vibrational-dephasing-time measurement

Toshiaki Hattori, Akira Terasaki, Takayoshi Kobayashi

A new method to measure picosecond or subpicosecond vibrational-dephasing dynamics with the use of incoherent or broadband light is presented theoretically and experimentally. It is based on a transient coherent Raman process with three beams. In our experimental scheme, two of them are incoherent light from a single source, and a delay time between the two is variable. A third beam has a higher frequency than the incoherent light by a vibrational energy in a molecule of interest, and is coherent in the delay-time range of the measurement. The delay-time dependence of coherent Stokes Raman scattering (CSRS) intensity offers the information about the coherence dynamics of the vibrational transition with a resolution time determined only by the correlation time of the incoherent light. For the theoretical calculation, a three-level model of the molecular system with homogeneous broadening is used, and delay-time dependences of the CSRS signal are calculated for off-resonance and resonance cases. Dephasing dynamics of the 2915-${\mathrm{cm}}^{\mathrm{\ensuremath{-}}1}$ mode in dimethylsulfoxide was observed experimentally by the new method with the use of nanosecond laser pulses, and the result agrees well with that obtained with picosecond pulses.

Physical Review A•Jan 1, 1987•94 citations

Scattering of Light by Resonating Molecules

RAYLEIGH

Nature•Nov 13, 1919•6 citations

Nonresonant scattering of intense light by a molecule

B. A. Zon, Boris G. Katsnelson

Journal of Experimental and Theoretical Physics•Oct 1, 1975•13 citations
The authors present a weak light field, scattering theoretical description of the intensity autocorrelation function for the scattered light from a many-atom (molecule) system. The theory considers both resonant and near-resonant scattering for atoms with many sublevels in both the ground and electronically excited states, and it incorporates the effects of the finite coherence time of the incident radiation. The theory is derived using incident two-photon wave packets with spatial dispersion among the target atoms. Purely anti-bunching contributions arise from single-atom-two-photon scattering and from successive two-atom-two-photon scattering events. However, there are interleaved two-atom-two-photon scattering processes which provide purely bunching contributions since both atoms may be scattering at the same time. Path length differences in the successive two-atom scatterings can also induce some bunching character to the correlation function. The dependence of the risetime and decay of the intensity correlation function upon the atomic excited state lifetimes and the coherence time of the incident light emphasises the correlation between photons which have been coherently and/or incoherently scattered.
A new method to measure picosecond or subpicosecond vibrational-dephasing dynamics with the use of incoherent or broadband light is presented theoretically and experimentally. It is based on a transient coherent Raman process with three beams. In our experimental scheme, two of them are incoherent light from a single source, and a delay time between the two is variable. A third beam has a higher frequency than the incoherent light by a vibrational energy in a molecule of interest, and is coherent in the delay-time range of the measurement. The delay-time dependence of coherent Stokes Raman scattering (CSRS) intensity offers the information about the coherence dynamics of the vibrational transition with a resolution time determined only by the correlation time of the incoherent light. For the theoretical calculation, a three-level model of the molecular system with homogeneous broadening is used, and delay-time dependences of the CSRS signal are calculated for off-resonance and resonance cases. Dephasing dynamics of the 2915-${\mathrm{cm}}^{\mathrm{\ensuremath{-}}1}$ mode in dimethylsulfoxide was observed experimentally by the new method with the use of nanosecond laser pulses, and the result agrees well with that obtained with picosecond pulses.