The dynamics of the hydrogen exchange reaction at 2.20 eV collision energy:: Comparison of experimental and theoretical differential cross sections

被引:86
作者
Wrede, E
Schnieder, L
Welge, KH
Aoiz, FJ
Bañares, L
Castillo, JF
Martínez-Haya, B
Herrero, VJ
机构
[1] Univ Bielefeld, Fak Phys, D-33501 Bielefeld, Germany
[2] Univ Complutense, Fac Quim, Dept Quim Fis, E-28040 Madrid, Spain
[3] CSIC, Inst Estructura Mat, E-28006 Madrid, Spain
关键词
D O I
10.1063/1.478870
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 H + D-2 (upsilon = 0, j = 0) --> HD(upsilon', j') + D isotopic variant of the hydrogen atom exchange reaction has been studied in a crossed molecular beam experiment at a collision energy of 2.20 eV. Kinetic energy spectra of the nascent D atoms were obtained by using the Rydberg atom time-of-flight technique. The extensive set of spectra collected has permitted the derivation of rovibrationally state-resolved differential cross sections in the center-of-mass frame for most of the internal states of the HD product molecules, allowing a direct comparison with theoretical predictions. Accurate 3D quantum mechanical calculations have been carried out on the refined version of the latest Boothroyd-Keogh-Martin-Peterson potential energy surface, yielding an excellent agreement with the experimentally determined differential cross sections. The comparison of the results from quasi-classical trajectory calculations on the same potential surface reveals some discrepancies with the measured data, but shows a good global accordance. The theoretical calculations demonstrate that, at this energy, reactive encounters are predominantly noncollinear and that collinear collisions lead mostly to nonreactive recrossing. The experimental results are satisfactorily accounted for by theoretical calculations without consideration of Geometric Phase effects. (C) 1999 American Institute of Physics. [S0021-9606(99)01420-8].
引用
收藏
页码:9971 / 9981
页数:11
相关论文
共 40 条
[1]   INTEGRAL RATE-CONSTANT MEASUREMENTS OF THE REACTION H+D2-]HD(UPSILON'=1,J')+D AT HIGH COLLISION ENERGIES [J].
ADELMAN, DE ;
XU, H ;
ZARE, RN .
CHEMICAL PHYSICS LETTERS, 1993, 203 (5-6) :573-577
[2]   The geometric phase effect in chemical reactions: A quasiclassical trajectory study [J].
Adhikari, S ;
Billing, GD .
JOURNAL OF CHEMICAL PHYSICS, 1997, 107 (16) :6213-6218
[3]   QUANTUM-MECHANICAL AND QUASI-CLASSICAL CALCULATIONS FOR THE H+D-2-]HD+D REACTION - REACTION PROBABILITIES AND DIFFERENTIAL CROSS SECTIONS [J].
AOIZ, FJ ;
BANARES, L ;
DMELLO, MJ ;
HERRERO, VJ ;
RABANOS, VS ;
SCHNIEDER, L ;
WYATT, RE .
JOURNAL OF CHEMICAL PHYSICS, 1994, 101 (07) :5781-5791
[4]   The H+D-2->HD+D reaction. Quasiclassical trajectory study of cross sections, rate constants, and kinetic isotope effect [J].
Aoiz, FJ ;
Banares, L ;
Herrero, VJ ;
Rabanos, VS ;
Tanarro, I .
JOURNAL OF PHYSICAL CHEMISTRY A, 1997, 101 (35) :6165-6176
[5]   QUASI-CLASSICAL STATE TO STATE REACTION CROSS-SECTIONS FOR D+H2(V=0, J=0)-]HD(V',J')+H - FORMATION AND CHARACTERISTICS OF SHORT-LIVED COLLISION COMPLEXES [J].
AOIZ, FJ ;
HERRERO, VJ ;
RABANOS, VS .
JOURNAL OF CHEMICAL PHYSICS, 1992, 97 (10) :7423-7436
[6]   Reaction cross section and rate constant calculations for the D+H-2(v=0,1)->HD+H reaction on three ab initio potential energy surfaces. A quasiclassical trajectory study [J].
Aoiz, FJ ;
Banares, L ;
DiezRojo, T ;
Herrero, VJ ;
Rabanos, VS .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (10) :4071-4083
[7]   Quasiclassical trajectory study of the H+D-2->HD+D reaction at a collision energy of 2.2 eV: A comparison with experimental results [J].
Aoiz, FJ ;
Banares, L ;
Herrero, VJ .
JOURNAL OF CHEMICAL PHYSICS, 1996, 105 (14) :6086-6087
[8]   THE D+H-2(V=1,J)-]HD(V'J')+H REACTION - A DETAILED QUASI-CLASSICAL TRAJECTORY STUDY [J].
AOIZ, FJ ;
BUCHENAU, HK ;
HERRERO, VJ ;
RABANOS, VS .
JOURNAL OF CHEMICAL PHYSICS, 1994, 100 (04) :2789-2799
[9]   EFFECTS OF TRANSLATIONAL, ROTATIONAL, AND VIBRATIONAL-ENERGY ON THE DYNAMICS OF THE D+H2 EXCHANGE-REACTION - A CLASSICAL TRAJECTORY STUDY [J].
AOIZ, FJ ;
HERRERO, VJ ;
RABANOS, VS .
JOURNAL OF CHEMICAL PHYSICS, 1991, 94 (12) :7991-8007
[10]  
AOIZ FJ, 1998, ADV CLASSICAL TRAJEC, V3