Real-Time Time-Dependent Nuclear-Electronic Orbital Approach: Dynamics beyond the Born-Oppenheimer Approximation

被引:52
|
作者
Zhao, Luning [2 ]
Tao, Zhen [1 ]
Pavosevic, Fabijan [1 ]
Wildman, Andrew [2 ]
Hammes-Schiffer, Sharon [1 ]
Li, Xiaosong [2 ]
机构
[1] Yale Univ, Dept Chem, 225 Prospect St, New Haven, CT 06520 USA
[2] Univ Washington, Dept Chem, Seattle, WA 98195 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2020年 / 11卷 / 10期
基金
美国国家科学基金会;
关键词
STATE PROTON-TRANSFER; MOLECULAR-DYNAMICS; FORMULATION;
D O I
10.1021/acs.jpclett.0c00701
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 mechanical treatment of both electrons and nuclei is crucial in nonadiabatic dynamical processes such as proton-coupled electron transfer. The nuclear-electronic orbital (NEO) method provides an elegant framework for including nuclear quantum effects beyond the Born-Oppenheimer approximation. To enable the study of nonequilibrium properties, we derive and implement a real-time NEO (RT-NEO) approach based on time-dependent Hatree-Fock or density functional theory, in which the electronic and nuclear degrees of freedom are propagated in a time-dependent variational framework. Nuclear and electronic spectral features can be resolved from the time-dependent dipole moment computed using the RT-NEO method. The test cases show the dynamical interplay between the quantum nuclei and the electrons through vibronic coupling. Moreover, vibrational excitation in the RT-NEO approach is demonstrated by applying a resonant driving field, and electronic excitation is demonstrated by simulating excited state intramolecular proton transfer. This work shows that the RT-NEO approach is a promising tool to study nonadiabatic quantum dynamical processes within a time-dependent variational description for the coupled electronic and nuclear degrees of freedom.
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页码:4052 / 4058
页数:7
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