Derivation of a true (t → 0+) quantum transition-state theory. I. Uniqueness and equivalence to ring-polymer molecular dynamics transition-state-theory

被引:107
作者
Hele, Timothy J. H. [1 ]
Althorpe, Stuart C. [1 ]
机构
[1] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
基金
英国工程与自然科学研究理事会;
关键词
CHEMICAL-REACTION RATES; THERMAL RATE CONSTANTS; STATISTICAL-MECHANICS; PATH; REPRESENTATION; BARRIERS; HYDROGEN; MODEL;
D O I
10.1063/1.4792697
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
Surprisingly, there exists a quantum flux-side time-correlation function which has a non-zero t -> 0(+) limit and thus yields a rigorous quantum generalization of classical transition-state theory (TST). In this Part I of two articles, we introduce the new time-correlation function and derive its t -> 0(+) limit. The new ingredient is a generalized Kubo transform which allows the flux and side dividing surfaces to be the same function of path-integral space. Choosing this function to be a single point gives a t -> 0(+) limit which is identical to an expression introduced on heuristic grounds by Wigner in 1932; however, this expression does not give positive-definite quantum statistics, causing it to fail while still in the shallow-tunnelling regime. Positive-definite quantum statistics is obtained only if the dividing surface is invariant to imaginary-time translation, in which case the t -> 0(+) limit is identical to ring-polymer molecular dynamics (RPMD) TST. The RPMD-TST rate is not a strict upper bound to the exact quantum rate, but is a good approximation to one if real-time coherence effects are small. Part II will show that the RPMD-TST rate is equal to the exact quantum rate in the absence of recrossing. (C) 2013 American Institute of Physics. [http://dx.doi.org/10.1063/1.4792697]
引用
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页数:13
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