The dynamics of the H+D2O→OD+HD reaction at 2.5 eV:: Experiment and theory

被引:19
作者
Brouard, M
Burak, I
Minayev, D
O'Keeffe, P
Vallance, C
Aoiz, FJ
Bañares, L
Castillo, JF
Zhang, DH
Collins, MA
机构
[1] Univ Oxford, Phys & Theoret Chem Lab, Dept Chem, Oxford OX1 3QZ, England
[2] Univ Complutense, Fac Quim, Dept Quim Fis, E-28040 Madrid, Spain
[3] Natl Univ Singapore, Dept Computat Sci, Singapore 119260, Singapore
[4] Australian Natl Univ, Res Sch Chem, Canberra, ACT 0200, Australia
关键词
D O I
10.1063/1.1528896
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 title reaction has been studied both experimentally and computationally at a mean collision energy of 2.48 eV. OD quantum state populations, rotational alignment parameters, rovibrational quantum state-resolved center-of-mass angular scattering distributions and HD co-product internal energy release distributions have been determined, along with OD quantum state averaged energy disposals. The experiments employ pulsed laser photolysis coupled with polarized Doppler-resolved laser induced fluorescence detection of the radical products. The OD angular scattering distributions show a preference for scattering in the forward direction, and are quite different from those observed previously at the lower collision energy of 1.4 eV. So too are the kinetic energy release distributions, which reveal that the HD co-products are born significantly more internally excited at 2.48 eV than at 1.4 eV. The HD internal energy distributions obtained from analysis of the Doppler resolved profiles are in reasonable accord with that derived from the direct HD population measurements performed by Zare and co-workers [J. Chem. Phys. 98, 4636 (1993)] at collision energies around 2.7 eV. The data are compared in detail with the results of new quasi-classical trajectory (QCT) calculations employing two alternative potential energy surfaces (PESs), as well as with the results from previous QCT studies of the title reaction by other workers. Refinements to the most recent of the PESs employed here, that developed using the iterative methods of Collins and Zhang and co-workers [J. Chem. Phys. 115, 174 (2001)], are also described. The theoretical results obtained using this refined PES agree very well with many of the experimental observables, and the surface appears to be a significant improvement on those previously developed. However, even with this new PES, the QCT calculations at 2.48 eV overestimate the internal excitation of the HD products. (C) 2003 American Institute of Physics.
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页码:1162 / 1174
页数:13
相关论文
共 109 条
[1]   INTEGRAL RATE-CONSTANT MEASUREMENTS OF THE REACTION H+D2O-]HD(V',J')+OD [J].
ADELMAN, DE ;
FILSETH, SV ;
ZARE, RN .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (06) :4636-4643
[2]   The dynamics of the reaction OH+D-2->HOD+D: Crossed beam experiments and quantum mechanical scattering calculations on ab initio potential energy surfaces [J].
Alagia, M ;
Balucani, N ;
Casavecchia, P ;
Stranges, D ;
Volpi, GG ;
Clary, DC ;
Kliesch, A ;
Werner, HJ .
CHEMICAL PHYSICS, 1996, 207 (2-3) :389-409
[3]   CROSSED BEAM STUDIES OF 4-ATOM REACTIONS - THE DYNAMICS OF OH+D2 [J].
ALAGIA, M ;
BALUCANI, N ;
CASAVECCHIA, P ;
STRANGES, D ;
VOLPI, GG .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (03) :2459-2462
[4]  
Alexander AJ, 1998, CHEM SOC REV, V27, P405
[5]  
Aoiz FJ, 1998, ADV CLAS TR, V3, P121
[6]   ANALYSIS OF PRODUCT DOPPLER-BROADENED PROFILES GENERATED FROM PHOTOINITIATED BIMOLECULAR REACTIONS [J].
AOIZ, FJ ;
BROUARD, M ;
ENRIQUEZ, PA ;
SAYOS, R .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1993, 89 (10) :1427-1434
[7]   Product rotational polarization in photon-initiated bimolecular reactions [J].
Aoiz, FJ ;
Brouard, M ;
Enriquez, PA .
JOURNAL OF CHEMICAL PHYSICS, 1996, 105 (12) :4964-4982
[8]   Rate coefficients for the reaction and relaxation of H2O in specific vibrational states with H atoms and H2O [J].
Barnes, PW ;
Sharkey, P ;
Sims, IR ;
Smith, IWM .
FARADAY DISCUSSIONS, 1999, 113 :167-180
[9]   The branching ratio between reaction and relaxation in the removal of H2O from its |04⟩- vibrational state in collisions with H atoms [J].
Barnes, PW ;
Sims, IR ;
Smith, IWM ;
Lendvay, G ;
Schatz, GC .
JOURNAL OF CHEMICAL PHYSICS, 2001, 115 (10) :4586-4592
[10]   Learning to interpolate molecular potential energy surfaces with confidence: A Bayesian approach [J].
Bettens, RPA ;
Collins, MA .
JOURNAL OF CHEMICAL PHYSICS, 1999, 111 (03) :816-826