Applications of a time correlation function theory for the fifth-order Raman response function I: Atomic liquids

被引:12
|
作者
DeVane, R
Ridley, C
Space, B
Keyes, T
机构
[1] Univ S Florida, Dept Chem, Tampa, FL 33620 USA
[2] Boston Univ, Dept Chem, Boston, MA 02215 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2005年 / 123卷 / 19期
基金
美国国家科学基金会;
关键词
D O I
10.1063/1.2038768
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
Multidimensional spectroscopy has the ability to provide great insight into the complex dynamics and time-resolved structure of liquids. Theoretically describing these experiments requires calculating the nonlinear-response function, which is a combination of quantum-mechanical time correlation functions (TCFs), making it extremely difficult to calculate. Recently, a new theory was presented in which the two-dimensional Raman quantum response function R-(5)(t(1),t(2)) was expressed with a two-time, computationally tractable, classical TCF. Writing the response function in terms of classical TCFs brings the full power of atomistically detailed molecular dynamics to the problem. In this paper, the new TCF theory is employed to calculate the fifth-order Raman response function for liquid xenon and investigate several of the polarization conditions for which experiments can be performed on an isotropic system. The theory is shown to reproduce line-shape characteristics predicted by earlier theoretical work. (c) 2005 American Institute of Physics.
引用
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页数:9
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