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
相关论文
共 113 条
[11]   TIME-DEPENDENT WAVEPACKET METHODS FOR THE CALCULATION OF COLLINEAR ATOM DIATOM EXCHANGE-REACTION PROBABILITIES [J].
BALAKRISHNAN, N ;
SATHYAMURTHY, N .
COMPUTER PHYSICS COMMUNICATIONS, 1991, 63 (1-3) :209-215
[12]   Time-dependent quantum mechanical approach to reactive scattering and related processes [J].
Balakrishnan, N ;
Kalyanaraman, C ;
Sathyamurthy, N .
PHYSICS REPORTS-REVIEW SECTION OF PHYSICS LETTERS, 1997, 280 (02) :79-144
[13]   FRACTALS AND RESONANCES IN COLLINEAR (HE,H2+) COLLISIONS [J].
BALASUBRAMANIAN, V ;
MISHRA, BK ;
BAHEL, A ;
KUMAR, S ;
SATHYAMURTHY, N .
JOURNAL OF CHEMICAL PHYSICS, 1991, 95 (06) :4160-4167
[14]   ISOTOPIC BRANCHING - EXPERIMENT VERSUS THEORY FOR HE+HD+ COLLISIONS [J].
BHALLA, KC ;
SATHYAMURTHY, N .
CHEMICAL PHYSICS LETTERS, 1989, 160 (04) :437-442
[15]   Exploring molecular motions in collinear HeH2+ and its isotopic variants using periodic orbits [J].
Bhatia, P ;
Maiti, B ;
Sathyamurthy, N ;
Stamatiadis, S ;
Farantos, SC .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1999, 1 (06) :1105-1113
[16]   EFFECT OF REAGENT ROTATION ON BIMOLECULAR COLLISIONS - H + H2(J) [J].
BOONENBERG, CA ;
MAYNE, HR .
CHEMICAL PHYSICS LETTERS, 1984, 108 (01) :67-70
[17]   NONEMPIRICAL LCAO-MO-SCF STUDY OF ENERGY SURFACE FOR LINEAR HEH2+ [J].
BROWN, PJ ;
HAYES, EF .
JOURNAL OF CHEMICAL PHYSICS, 1971, 55 (02) :922-&
[18]   OPEN AND CLOSED CHANNEL RESONANCES IN COLLINEAR INELASTIC-SCATTERING OF HE BY H-2(+) [J].
CHAPMAN, FM ;
HAYES, EF .
JOURNAL OF CHEMICAL PHYSICS, 1976, 65 (03) :1032-1034
[19]   RESONANCES IN COLLINEAR INELASTIC-SCATTERING OF HE BY H+-2 BELOW REACTION THRESHOLD [J].
CHAPMAN, FM ;
HAYES, EF .
JOURNAL OF CHEMICAL PHYSICS, 1975, 62 (11) :4400-4403
[20]  
Chupka W. A., 1969, 6th International conference on the physics of electronic and atomic collisions (abstracts), P71