Further partitioning of the reactant-product decoupling equations of state-to-state reactive scattering and their solution by the time-independent wave-packet method

被引:50
作者
Althorpe, SC
Kouri, DJ
Hoffman, DK
机构
[1] UNIV HOUSTON,DEPT PHYS,HOUSTON,TX 77204
[2] IOWA STATE UNIV SCI & TECHNOL,DEPT CHEM,AMES,IA 50011
[3] IOWA STATE UNIV SCI & TECHNOL,AMES LAB,AMES,IA 50011
关键词
D O I
10.1063/1.475095
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 reactant-product decoupling (RPD) equations are a rigorous formulation of state-to-state reactive scattering recently introduced by Peng and Zhang. For an N-arrangement reaction there are a total of N RPD equations, each of which describes the dynamics in just one region of coordinate space. One of the regions (the r-region) encloses the reactant channel and the strong interaction region; each of the other N - 1 regions encloses one of the product channels. In this paper we develop a suggestion later made by Kouri and co-workers: that the original RPD equations can be further partitioned into a set of new RPD equations, in which the original r-region is now partitioned into three regions-two enclosing the reactant channel, and one enclosing the strong interaction region. After introducing the new RPD equations, we derive the time-independent wave-packet (TIW) form of the equations, and show how to solve them using an extended version of the Chebyshev propagator. We test the new RPD equations (and the method) by calculating state-to-state reaction probabilities and inelastic probabilities for the three-dimensional (J = 0) H + H-2 reaction. (C) 1997 American Institute of Physics.
引用
收藏
页码:7816 / 7824
页数:9
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