An equauon for ribrallonal dcphxsmg rail~es II-I hqmds conwuung the effccu of molecular oricnwnons and attraction has been dernxd by use of tbe bmary colla~on model Lkphxing rates are found to be a strong function of the orrntauon angle of vrbrating molecules. For Lqurd rulrogeen. the mcluston of or
Dephasing processes of molecular vibrations in liquids
β Scribed by S.F. Fischer; A. Laubereau
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- English
- Weight
- 765 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
A model based on :iemiclassical collision theory is presented to describe the dephasing of vibrationally excited molecules in a Iiquid. It is sholvn that fluctuations of the vibrational frequencies, which are uuzed by the intermolecular interaction, lead to phase rc:laxation of 3 coherently excited stiite. The theoretic4 restits compare favorably with data of ?he vibratio_ti tiephasing time measured with picosecond probing techniques. The relationship between the dephasing time and the linewidths observed in IR and F&man spectroscopy is discussed.
π SIMILAR VOLUMES
Raman spectra are reported for the v1 bands of germane and germane-d,. Fourier transformation of the band shapes provided vibrational autocorrelation functions. These functions were modeled by a memory-function procedure. Evidence for resonant vibrational energy transfer and higher order cumulant-ex
We consider a simple closure for the contmued-Iracnon expansion of the \lbra:lonal correlation function IX contams no adJustable parameters. yet shows remarkable agreement w~tb expenmental data lor some molecules m the hquld phase