期刊
JOURNAL OF CHEMICAL PHYSICS
卷 132, 期 17, 页码 -出版社
AMER INST PHYSICS
DOI: 10.1063/1.3408288
关键词
optical Kerr effect; organic compounds; Raman spectra; spectral line shift; time resolved spectra
资金
- EPSRC [EP/E010466/1]
- EPSRC [EP/E010466/1] Funding Source: UKRI
- Engineering and Physical Sciences Research Council [EP/E010466/1] Funding Source: researchfish
The Raman spectra below 300 wavenumbers of six different aromatic molecular liquids have been measured with a time and polarization resolved optical Kerr effect technique. The isotropic and anisotropic contributions were determined to yield the complete third order response, and thus a more detailed description of the microscopic liquid dynamics. The anisotropic contributions accurately reproduced previously published results. Both the isotropic and anisotropic Raman spectral densities shift toward lower frequencies with decreasing molecular weights. The first moment of the isotropic spectral densities scales linearly with the inverse square root of the molecular weight, which is consistent with interaction-induced dynamics in these liquids being driven mainly by motions with a translational character. Also, the isotropic spectral densities could be fit to a single Bucaro-Litovitz function. The exponent delta of this function increases monotonically with the inverse square root of the molecular weight. A possible physical origin of this behavior is discussed. (c) 2010 American Institute of Physics. [doi: 10.1063/1.3408288]
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