Modeling of ultrafast electron-transfer processes: Validity of multilevel Redfield theory

被引:140
作者
Egorova, D [1 ]
Thoss, M
Domcke, W
Wang, HB
机构
[1] Tech Univ Munich, Inst Phys & Theoret Chem, D-85748 Garching, Germany
[2] New Mexico State Univ, Dept Chem & Biochem, Las Cruces, NM 88003 USA
关键词
D O I
10.1063/1.1587121
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
The capability of multilevel Redfield theory to describe ultrafast photoinduced electron-transfer reactions is investigated. Adopting a standard model of photoinduced electron transfer in a condensed-phase environment, we consider electron-transfer reactions in the normal and inverted regimes, as well as for different values of the electron-transfer parameters, such as reorganization energy, electronic coupling, and temperature. Based on the comparison with numerically exact reference results, obtained using the self-consistent hybrid method, we discuss in some detail the advantages and shortcomings of two different versions of Redfield theory, which employ the time-dependent and stationary Redfield tensor, respectively. The results of the study demonstrate that multilevel Redfield theory, if applied in the appropriate parameter regime, is well suited to describe the ultrafast coherent dynamics of photoinduced electron-transfer reactions. (C) 2003 American Institute of Physics.
引用
收藏
页码:2761 / 2773
页数:13
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