Application of the time-independent wave packet reactant-product decoupling method to the (J=0) Li+HF reaction

被引:28
作者
Althorpe, SC
Kouri, DJ
Hoffman, DK
机构
[1] Univ Houston, Dept Chem, Houston, TX 77204 USA
[2] Univ Houston, Dept Phys, Houston, TX 77204 USA
[3] Iowa State Univ, Dept Chem, Ames, IA 50011 USA
[4] Iowa State Univ, Ames Lab, Ames, IA 50011 USA
关键词
D O I
10.1021/jp981992m
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 time-independent wave packet reactant-product decoupling (TIW-RPD) method is a new method for calculating state-to-state reaction probabilities, which we recently developed by extending the original reactant-product decoupling method of Peng and Zhang (Peng, T.; Zharg, J. Z. H. J. Chem. Phys. 1996, 105, 6072; Zhu, W.; Peng, T.; Zhang, J. Z. H. J. Chem. Phys. 1997, 106, 1742). In the TIW-RPD method, the nuclear dynamics Schroedinger equation is partitioned into a set of completely decoupled equations, each of which describes the nuclear dynamics in either the reactant channel, one of the product channels, or the strong-interaction region. In this paper we apply the TIW-RPD method to the (three-dimensional) Li + HF --> LiF + H (J = 0) reaction. We also describe an improvement to the reactant channel part of the method. The state-to-state reaction probabilities for Li + HF converge very well with respect to the size of the strong-interaction region, demonstrating that the TIW-RPD method is robust enough to be applied to a wide range of chemical reactions, including those in which the dynamics are influenced by a long-range potential energy surface.
引用
收藏
页码:9494 / 9499
页数:6
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