Exciton dissociation at donor-acceptor polymer heterojunctions: Quantum nonadiabatic dynamics and effective-mode analysis

被引:60
|
作者
Tamura, Hiroyuki
Bittner, Eric R.
Burghardt, Irene
机构
[1] Ecole Normale Super, Dept Chim, F-75231 Paris 05, France
[2] Univ Houston, Dept Chem, Houston, TX 77204 USA
[3] Univ Houston, Texas Ctr Superconduct, Houston, TX 77204 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2007年 / 126卷 / 02期
基金
美国国家科学基金会;
关键词
D O I
10.1063/1.2431358
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 quantum-dynamical mechanism of photoinduced subpicosecond exciton dissociation and the concomitant formation of a charge-separated state at a semiconducting polymer heterojunction is elucidated. The analysis is based upon a two-state vibronic coupling Hamiltonian including an explicit 24-mode representation of a phonon bath comprising high-frequency (C = C stretch) and low-frequency (torsional) modes. The initial relaxation behavior is characterized by coherent oscillations, along with the decay through an extended nonadiabatic coupling region. This region is located in the vicinity of a conical intersection hypersurface. A central ingredient of the analysis is a novel effective mode representation, which highlights the role of the low-frequency modes in the nonadiabatic dynamics. Quantum dynamical simulations were carried out using the multiconfiguration time-dependent Hartree method. (c) 2007 American Institute of Physics.
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页数:5
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