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Isotopic branching in (He, HD+) collisions:: A time-dependent quantum mechanical study in three dimensions
被引:31
作者:
Kalyanaraman, C
Clary, DC
Sathyamurthy, N
机构:
[1] Univ London Univ Coll, Dept Chem, London WC1H 0AJ, England
[2] Indian Inst Technol, Dept Chem, Kanpur 208016, Uttar Pradesh, India
关键词:
D O I:
10.1063/1.480454
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:
A time-dependent quantum mechanical approach has been used to investigate the reaction He+HD+(v=0-4,j=0-3)--> HeH++D; HeD++H in three dimensions for total angular momentum J=0. The vib-rotation (v,j) state-selected reaction probability (P-v,j(R)) is shown to increase with v over the collision energy (E-trans) range (0.95-2.25 eV) investigated for both the exchange channels, in accord with the experimental results. The isotopic branching ratio Gamma=P-R(HeH+)/P-R(HeD+) generally remains less than unity for different v states at different E-trans in agreement with experiment. But at E-trans=1.0 eV, for v=4, Gamma obtained from our calculations for j=0 of HD+ is similar to 0.8, in excellent agreement with the earlier quasiclassical trajectory calculations, but a factor of 2 less than that obtained from experiment. This difference could arise from the inclusion of nonzero j states in the experimental study, as P-v,j(R) is found to be j dependent for both the channels. While P-v,j(R) (HeH+) decreases initially with increase in j from 0 to 2 and then increases when j is increased further to 3, P-v,j(R) (HeD+) reveals an unusual j dependence; it is larger for even j states of HD+ than for odd j. As a result, Gamma is strongly dependent on j, in contrast to the marginal dependence shown by the earlier quasiclassical trajectory calculations. (C) 1999 American Institute of Physics. [S0021- 9606(99)00547-4].
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页码:10910 / 10918
页数:9
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