Path integral Liouville dynamics for thermal equilibrium systems

被引:36
|
作者
Liu, Jian [1 ]
机构
[1] Peking Univ, Coll Chem & Mol Engn, Inst Theoret & Computat Chem, Beijing Natl Lab Mol Sci, Beijing 100871, Peoples R China
来源
JOURNAL OF CHEMICAL PHYSICS | 2014年 / 140卷 / 22期
基金
美国国家科学基金会;
关键词
VIBRATIONAL-ENERGY RELAXATION; BACKWARD SEMICLASSICAL DYNAMICS; CENTROID MOLECULAR-DYNAMICS; TIME-CORRELATION-FUNCTIONS; QUANTUM-STATISTICAL MECHANICS; LIQUID PARA-HYDROGEN; RATE CONSTANTS; ALGORITHMS; SIMULATION; APPROXIMATION;
D O I
10.1063/1.4881518
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 show a new imaginary time path integral based method-path integral Liouville dynamics (PILD), which can be derived from the equilibrium Liouville dynamics [J. Liu and W. H. Miller, J. Chem. Phys. 134, 104101 (2011)] in the Wigner phase space. Numerical tests of PILD with the simple (white noise) Langevin thermostat have been made for two strongly anharmonic model problems. Since implementation of PILD does not request any specific form of the potential energy surface, the results suggest that PILD offers a potentially useful approach for general condensed phase molecular systems to have the two important properties: conserves the quantum canonical distribution and recovers exact thermal correlation functions (of even nonlinear operators, i.e., nonlinear functions of position or momentum operators) in the classical, high temperature, and harmonic limits. (C) 2014 AIP Publishing LLC.
引用
收藏
页数:11
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