Quantum transition state theory: Perturbation expansion

被引:87
作者
Shao, JS [1 ]
Liao, JL
Pollak, E
机构
[1] Nankai Univ, Nankai Inst Math, Tianjin 300071, Peoples R China
[2] Univ Augsburg, Inst Phys, D-86135 Augsburg, Germany
[3] Weizmann Inst Sci, Dept Chem Phys, IL-76100 Rehovot, Israel
[4] Univ Sci & Technol China, Hefei 230026, Peoples R China
关键词
D O I
10.1063/1.476446
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 exact quantum expression for the thermal rate of reaction is the trace of a product of two operators. It may therefore be written exactly as a phase space integral over the Wigner phase space representations of the two operators. The two are a projection operator onto the product's space, which is difficult to compute, and the symmetrized thermal flux operator, which can be computed using Monte Carlo methods. A quantum transition state theory was presented recently, in which the exact projection operator was replaced by its parabolic barrier limit. Alternatively, the exact projection operator may be replaced by its classical limit. Both approximations give thermodynamic estimates for the quantum rates. In this paper, we derive a perturbation theory expansion for the projection operator about the parabolic barrier limit and the classical limit. The correction terms are then used to evaluate the leading order corrections to the rate estimates based on the parabolic barrier or classical limits of the projection operator. The expansion is applied to a symmetric and an asymmetric Eckart barrier. The first two terms in the expansion give excellent results for temperatures above the crossover between quantum tunneling and thermal activation. For deep tunneling and asymmetric systems, the use of variational transition state theory, the classical limit, and perturbation theory leads to significant improvement in the estimate of the tunneling rate. Multidimensional extensions are presented and discussed. (C) 1998 American Institute of Physics.
引用
收藏
页码:9711 / 9725
页数:15
相关论文
共 34 条
[1]  
[Anonymous], DYNAMICS MOL COLLI B
[2]   A unified framework for quantum activated rate processes .1. General theory [J].
Cao, JS ;
Voth, GA .
JOURNAL OF CHEMICAL PHYSICS, 1996, 105 (16) :6856-6870
[3]   SEMICLASSICAL TRANSITION-STATE THEORY FOR NONSEPARABLE SYSTEMS - APPLICATION TO COLLINEAR H+H2 REACTION [J].
CHAPMAN, S ;
GARRETT, BC ;
MILLER, WH .
JOURNAL OF CHEMICAL PHYSICS, 1975, 63 (06) :2710-2716
[4]  
DATTAGUPTA S, 1987, RELAXATION PHENOMENA, P27
[5]   EQUILIBRIUM AND DYNAMICAL FOURIER PATH INTEGRAL METHODS [J].
Doll, J. D. ;
Freeman, David L. ;
Beck, Thomas L. .
ADVANCES IN CHEMICAL PHYSICS <D>, 1990, 78 :61-127
[6]   The activated complex in chemical reactions [J].
Eyring, H .
JOURNAL OF CHEMICAL PHYSICS, 1935, 3 (02) :107-115
[7]   ACTIVATED RATE-PROCESSES - ANHARMONIC CORRECTIONS TO THE QUANTUM RATE [J].
GEORGIEVSKII, Y ;
POLLAK, E .
JOURNAL OF CHEMICAL PHYSICS, 1995, 103 (20) :8910-8920
[8]   VARIATIONAL TRANSITION-STATE THEORY - APPLICATION TO A SYMMETRICAL EXCHANGE-REACTION IN WATER [J].
GERSHINSKY, G ;
POLLAK, E .
JOURNAL OF CHEMICAL PHYSICS, 1995, 103 (19) :8501-8512
[9]   QUANTUM CLASSICAL CROSSOVER OF THE TRANSITION RATE IN THE DAMPED DOUBLE WELL [J].
GILLAN, MJ .
JOURNAL OF PHYSICS C-SOLID STATE PHYSICS, 1987, 20 (24) :3621-3641
[10]  
HANGGI P, 1990, REV MOD PHYS, V62, P251, DOI 10.1103/RevModPhys.62.251