Cumulative reaction probabilities:: A comparison between quasiclassical and quantum mechanical results

被引:21
作者
Aoiz, F. J. [1 ]
Brouard, M.
Eyles, C. J.
Castillo, J. F.
Rabanos, V. Saez
机构
[1] Univ Complutense Madrid, Fac Quim, Dept Quim Fis, E-28040 Madrid, Spain
[2] Univ Oxford, Dept Chem, Phys & Theoret Chem Lab, Oxford OX1 3QZ, England
[3] Univ Politecn Madrid, Dept Quim & Bioquim, ETS Ingn Montes, E-28040 Madrid, Spain
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1063/1.2353837
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
This article presents a quasiclassical trajectory (QCT) method for determining the cumulative reaction probability (CRP) as a function of the total energy. The method proposed is based on a discrete sampling using integer values of the total and orbital angular momentum quantum numbers for each trajectory and on the development of equations that have a clear counterpart in the quantum mechanical (QM) case. The calculations comprise cumulative reaction probabilities at a given total angular momentum J, as well as those summed over J. The latter are used to compute QCT rate constants. The method is illustrated by comparing QCT and exact QM results for the H+H-2, H+D-2, D+H-2, and H+HD reactions. The agreement between QCT and QM results is very good, with small discrepancies between the two data sets indicating some genuine quantum effects. The most important of these involves the value of the CRP at low energies which, due to the absence of tunneling, is lower in the QCT calculations, causing the corresponding rate constants to be smaller. The second is the steplike structure that is clearly displayed in the QM CRP for J=0, which is much smoother in the corresponding QCT results. However, when the QCT density of reactive states, i.e., the derivatives of the QCT CRP with respect to the energy, is calculated, a succession of maxima and minima is obtained which roughly resembles those found in the QM calculations, although the latter are considerably sharper. The analysis of the broad peaks in the QCT density of reactive states indicates that the distributions of collision times associated with the maxima are somewhat broader, with a tail extending to larger collision times, than those associated with the minima. In addition, the QM and QCT dynamics of the isotopic variants mentioned above are compared in the light of their CRPs. Issues such as the compliance of the QCT CRP with the law of microscopic reversibility, as well as the similarity between the CRPs for ortho and para species in the QM and QCT cases, are also addressed. (c) 2006 American Institute of Physics.
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页数:14
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共 53 条
[1]   Time-dependent plane wave packet formulation of quantum scattering with application to H+D2→HD+D [J].
Althorpe, SC .
JOURNAL OF CHEMICAL PHYSICS, 2002, 117 (10) :4623-4627
[2]   Quasiclassical determination of reaction probabilities as a function of the total angular momentum -: art. no. 094101 [J].
Aoiz, FJ ;
Sáez-Rábanos, V ;
Martínez-Haya, B ;
González-Lezana, T .
JOURNAL OF CHEMICAL PHYSICS, 2005, 123 (09)
[3]   THE F+HD-]DF(HF)+H(D) REACTION REVISITED - QUASI-CLASSICAL TRAJECTORY STUDY ON AN AB-INITIO POTENTIAL-ENERGY SURFACE AND COMPARISON WITH MOLECULAR-BEAM EXPERIMENTS [J].
AOIZ, FJ ;
BANARES, L ;
HERRERO, VJ ;
RABANOS, VS ;
STARK, K ;
WERNER, HJ .
JOURNAL OF CHEMICAL PHYSICS, 1995, 102 (23) :9248-9262
[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]   Recent results from quasiclassical trajectory computations of elementary chemical reactions [J].
Aoiz, FJ ;
Banares, L ;
Herrero, VJ .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1998, 94 (17) :2483-2500
[8]   The H+H2 reactive system.: Progress in the study of the dynamics of the simplest reaction [J].
Aoiz, FJ ;
Bañares, L ;
Herrero, VJ .
INTERNATIONAL REVIEWS IN PHYSICAL CHEMISTRY, 2005, 24 (01) :119-190
[9]   Quantum mechanical rate constants for the D+H-2->HD+H reaction on the BKMP2 potential energy surface [J].
Banares, L ;
DMello, MJ .
CHEMICAL PHYSICS LETTERS, 1997, 277 (5-6) :465-472
[10]   QUASICLASSICAL TRAJECTORY (AND VARIATIONAL TRANSITION-STATE THEORY) STUDY OF THE RATES AND TEMPERATURE-DEPENDENT ACTIVATION-ENERGIES OF THE REACTIONS MU+H2 (COMPLETELY THERMAL) AND H,D, AND MU+H2 (V=0,J=2) [J].
BLAIS, NC ;
TRUHLAR, DG ;
GARRETT, BC .
JOURNAL OF CHEMICAL PHYSICS, 1983, 78 (05) :2363-2367