Multi-configurational Ehrenfest simulations of ultrafast nonadiabatic dynamics in a charge-transfer complex

被引:18
作者
Ma, Tianji [1 ]
Bonfanti, Matteo [1 ]
Eisenbrandt, Pierre [1 ]
Martinazzo, Rocco [2 ]
Burghardt, Irene [1 ]
机构
[1] Goethe Univ Frankfurt, Inst Phys & Theoret Chem, Max von Laue Str 7, D-60438 Frankfurt, Germany
[2] Univ Milan, Dept Chem, Via Golgi 19, I-20133 Milan, Italy
关键词
PHOTOINDUCED ELECTRON-TRANSFER; MOLECULAR-DYNAMICS; ENERGY RELAXATION; QUANTUM; DISSOCIATION; SPECTROSCOPY; FORMULATION; COLLISIONS; ALGORITHM; STATES;
D O I
10.1063/1.5062608
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
Multi-configurational Ehrenfest (MCE) approaches, which are intended to remedy the lack of correlations in the standard mean-field Ehrenfest method, have been proposed as coherent-state based ansatze for quantum propagation [D. V. Shalashilin, J. Chem. Phys. 130, 244101 (2009)] and also as the classical limit of the variational Gaussian-based multiconfiguration time dependent Hartree (G-MCTDH) method [S. Romer and I. Burghardt, Mol. Phys. 111, 3618 (2013)]. In the present paper, we establish the formal connection between these schemes and assess the performance of MCE for a coherent-state representation of the classical-limit subsystem. As a representative model system, we address the ultrafast, coherent charge transfer dynamics in an oligothiophene-fullerene donor acceptor complex described by a two-state linear vibronic coupling model. MCE calculations are compared with reference calculations performed with the MC IDH method, for 10-40 vibrational modes. Beyond a dimensionality of 10 modes, it is shown that the correct representation of electronic coherence depends crucially on the sampling of initially unoccupied Gaussians. Published by AIP Publishing.
引用
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页数:13
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