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 Molecular Structure

Picosecond dephasing of coherently excited vibrations in liquid N2/ar mixtures

Jan Langelaar, H. M. M. Hesp, Dick Bebelaar, Joop D. W. van Voorst

Published Jan 1, 1978• 0 citations
Publisher
DOI
10.1016/0022-2860(78)87081-1

Related papers

Picosecond Dephasing of Coherently Excited Vibrational Levels in Liquid N2/Ar Mixtures

Joop D. W. van Voorst, H. M. M. Hesp, Jan Langelaar +1 more

Springer eBooks•Jan 1, 1978•0 citations

Collective beating of molecular vibrations in liquids on the picosecond time scale

A. Laubereau, G. Wochner, W. Kaiser

Optics Communications•Apr 1, 1976•38 citations

Raman echo studies of vibrational dephasing in liquids

Mark A. Berg, Laura Müller, David Vanden Bout

Quantum Electronics and Laser Science Conference•May 10, 1992•0 citations

Picosecond Photon Echo and Coherent Raman Scattering Studies of Dephasing in Mixed Molecular Crystals

Koos Duppen, D. P. Weitekamp, D. A. Wiersma

Springer series in chemical physics•Jan 1, 1982•0 citations

Coherent pulsations in the vibrational fluorescence of CO and NO in solid N2

J.‐J. Zondy, Jean‐Pierre Galaup, Henri Dubost

Journal of Luminescence•Dec 1, 1987•7 citations

Suppression of vibron state formation in Arx(N2)1−x mixed crystals

Jan De Kinder, A. Bouwen, E. Goovaerts +1 more

The dephasing of the k≂0 states of the vibrons in Arx(N2)1−x crystals was studied by picosecond time-resolved coherent anti-Stokes Raman scattering as a function of temperature (0<T<40 K) and Ar concentration (0<x<0.15). Homogeneous (exponential) and inhomogeneous (Gaussian) contributions to the observed dephasing signal were separated. In the α phase, an increase of the inhomogeneous linewidth was obtained starting from small concentrations of Ar atoms. For larger Ar concentrations, a decrease of the exponential dephasing time T2 and a temperature dependence of the increasingly faster Gaussian decay is observed. Substitution of N2 molecules by Ar atoms increases the librational amplitude. Through anharmonic terms in the crystal Hamiltonian the vibron state formation is reduced and as a result, the T2 time decreases. This suppression of vibron state formation, which counteracts the reduction of the inhomogeneous broadening, is responsible for the increasing and temperature dependent inhomogeneous linewidth. The Ag−Tg factor group splitting increases almost linearly with Ar concentration. Surprisingly, no inhomogeneous line broadening could be resolved for β-Arx(N2)1−x crystals and the observed dephasing time T2 remains long compared to the α phase, even for high Ar concentrations.

The Journal of Chemical Physics•Aug 15, 1991•14 citations
The dephasing of the k≂0 states of the vibrons in Arx(N2)1−x crystals was studied by picosecond time-resolved coherent anti-Stokes Raman scattering as a function of temperature (0<T<40 K) and Ar concentration (0<x<0.15). Homogeneous (exponential) and inhomogeneous (Gaussian) contributions to the observed dephasing signal were separated. In the α phase, an increase of the inhomogeneous linewidth was obtained starting from small concentrations of Ar atoms. For larger Ar concentrations, a decrease of the exponential dephasing time T2 and a temperature dependence of the increasingly faster Gaussian decay is observed. Substitution of N2 molecules by Ar atoms increases the librational amplitude. Through anharmonic terms in the crystal Hamiltonian the vibron state formation is reduced and as a result, the T2 time decreases. This suppression of vibron state formation, which counteracts the reduction of the inhomogeneous broadening, is responsible for the increasing and temperature dependent inhomogeneous linewidth. The Ag−Tg factor group splitting increases almost linearly with Ar concentration. Surprisingly, no inhomogeneous line broadening could be resolved for β-Arx(N2)1−x crystals and the observed dephasing time T2 remains long compared to the α phase, even for high Ar concentrations.