Real-Space and Real-Time Propagation for Correlated Electron-Nuclear Dynamics Based on Exact Factorization

被引:6
|
作者
Han, Daeho [1 ]
Ha, Jong-Kwon [1 ]
Min, Seung Kyu [1 ]
机构
[1] Ulsan Natl Inst Sci & Technol UNIST, Sch Nat Sci, Dept Chem, Ulsan 44919, South Korea
基金
新加坡国家研究基金会;
关键词
DENSITY-FUNCTIONAL THEORY; MOLECULAR-DYNAMICS; CONSTANT;
D O I
10.1021/acs.jctc.2c00939
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
We present coupled equations of motion for correlated electron-nuclear dynamics for real-space and real-time propagation with a proper electron-nuclear correlation (ENC) from the exact factorization. Since the original ENC term from the exact factorization is non-Hermitian, the numerical instability arises as we propagate an electronic wave function. In this paper, we propose a Hermitian-type ENC term which depends on the electron density matrix and the nuclear quantum momentum. Moreover, we show that the Hermitian property of the electron- nuclear correlation term can capture quantum (de)coherence with a stable numerical real-space and real-time propagation. As an application, we demonstrate a real-space and real-time propagation of an electronic wave function coupled to trajectory-based nuclear motion for a one-dimensional model Hamiltonian. Our approach can capture nonadiabatic phenomena as well as quantum decoherence in excited state molecular dynamics. In addition, we propose a scheme to extend the current approach to many-body electronic states based on real-time time-dependent density functional theory, testing the nonadiabatic dynamics of a simple molecular system.
引用
收藏
页码:2186 / 2197
页数:12
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