VIBRATIONAL FREQUENCIES AND DEPHASING TIMES IN EXCITED ELECTRONIC STATES BY FEMTOSECOND TIME-RESOLVED 4-WAVE-MIXING

被引:42
作者
JOO, TH
ALBRECHT, AC
机构
[1] Department of Chemistry, Baker Laboratory, Cornell University, Ithaca
关键词
D O I
10.1016/0301-0104(93)80213-S
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Time-resolved degenerate four-wave mixing (TRDFWM) for an electronically resonant system in a phase-matching configuration that measures population decay is reported- Because the spectral width of input light exceeds the vibrational Bohr frequency of a strong Raman active mode, the vibrational coherence produces strong oscillations in the TRDFWM signal together with the usual population decay from the excited electronic state. The data are analyzed in terms of a four-level system: ground and excited electronic states each split by a vibrational quantum of a Raman active mode. Absolute frequencies and their dephasing times of the vibrational modes at almost-equal-to 5 90 cm-1 are obtained for the excited as well as the ground electronic state. The vibrational dephasing rate in the excited electronic state is about an order of magnitude faster than that in the ground state, the origin of which is speculated upon.
引用
收藏
页码:17 / 26
页数:10
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