Time-dependent wave packet theory for state-to-state differential cross sections of four-atom reactions in full dimensions: Application to the HD+OH → H2O+D reaction

被引:62
作者
Liu, Shu [1 ]
Xu, Xin
Zhang, Dong H.
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Mol React Dynam, Dalian 116023, Peoples R China
基金
中国国家自然科学基金;
关键词
CENTRIFUGAL SUDDEN APPROXIMATION; POTENTIAL-ENERGY SURFACES; QUANTUM-MECHANICAL CALCULATION; DIATOM-DIATOM REACTIONS; REACTION PROBABILITIES; REACTION DYNAMICS; H-2+OH REACTION; BIMOLECULAR REACTION; INSERTION REACTION; RATE CONSTANTS;
D O I
10.1063/1.3701266
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
Time-dependent wave packet method has been developed to calculate differential cross section for four-atom reactions in full dimension, utilizing an improved version of reactant-product-decoupling scheme. Differential cross sections for the title reaction were calculated for collision energy up to 0.4 eV. It is found that the differential cross sections for the reaction are all peaked in the backward direction. The majority of H2O is produced in the first stretch excited state, with a large fraction of available energy for the reaction going into H2O internal motion. As compared in a previous report by Xiao et al. [Science 333, 440 ( 2011)], the differential cross section at E-c = 0.3 eV and the differential cross section at the backward direction as a function of collision energy agree with experiment very well, indicating it is possible now to calculate complete dynamical information for some simple four-atom reactions, as have been done for three-atom reactions in the past decades. (C) 2012 American Institute of Physics. [http://dx.doi.org/10.1063/1.3701266]
引用
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页数:10
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