Stochastic Liouville equations for femtosecond stimulated Raman spectroscopy

被引:9
作者
Agarwalla, Bijay Kumar [1 ]
Ando, Hideo [1 ]
Dorfman, Konstantin E. [1 ]
Mukamel, Shaul [1 ]
机构
[1] Univ Calif Irvine, Dept Chem, Irvine, CA 92717 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
MULTIPHOTON INTRAPULSE INTERFERENCE; EXCITED-STATE DYNAMICS; STRUCTURAL EVOLUTION; MOLECULAR-DYNAMICS; PROTON-TRANSFER; LASER-PULSES; MODEL;
D O I
10.1063/1.4905139
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
Electron and vibrational dynamics of molecules are commonly studied by subjecting them to two interactions with a fast actinic pulse that prepares them in a nonstationary state and after a variable delay period T, probing them with a Raman process induced by a combination of a broadband and a narrowband pulse. This technique, known as femtosecond stimulated Raman spectroscopy (FSRS), can effectively probe time resolved vibrational resonances. We show how FSRS signals can be modeled and interpreted using the stochastic Liouville equations (SLE), originally developed for NMR lineshapes. The SLE provide a convenient simulation protocol that can describe complex dynamics caused by coupling to collective bath coordinates at much lower cost than a full dynamical simulation. The origin of the dispersive features that appear when there is no separation of time-scales between vibrational variations and the dephasing time is clarified. (C) 2015 AIP Publishing LLC.
引用
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页数:10
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