Forward scattering in the H+D2→HD+D reaction:: Comparison between experiment and theoretical predictions

被引:34
作者
Fernández-Alonso, F
Bean, BD
Zare, RN
Aoiz, FJ
Bañares, L
Castillo, JF
机构
[1] CNR, Ist Struttura Mat, I-00133 Rome, Italy
[2] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[3] Univ Complutense, Fac Quim, Dept Quim Fis, E-28040 Madrid, Spain
关键词
D O I
10.1063/1.1390505
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
We investigate the sensitivity of photoinitiated experiments to forward-scattering features by direct comparison of experimental angular distributions with quantum-mechanical calculations as well as by forward-convolution of theoretical and model center-of-mass differential cross sections. We find that the experimental sensitivity to forward-scattering angles depends on the instrumental velocity resolution as well as on the kinematics of the detected product channel. Explicit comparison is made between experimental HD(v(')=1,2;j(')) center-of-mass angular distributions at collision energies approximate to1.6 eV (deduced from time-of-flight profiles using a single-laser, photolysis-probe approach) and quantum-mechanical calculations on the BKMP2 potential energy surface. The comparison takes into account the contributions from both slow and fast H atoms from the photolysis of HBr. We find that the contribution of the slow H atoms, which is the major source of experimental uncertainty, does not greatly affect the extraction of the angular distribution from the experimental time-of-flight profile for a specific HD(v('),j(')) state. Except for HD(v(')=1, j(')=8) and HD(v(')=2, j(')=0), for which either slow H atoms or the presence of a narrow forward-scattering peak make the analysis more uncertain, the agreement between experiment and theoretical predictions is excellent. (C) 2001 American Institute of Physics.
引用
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页码:4534 / 4545
页数:12
相关论文
共 37 条
  • [11] Fernández-Alonso F, 2000, ANGEW CHEM INT EDIT, V39, P2748, DOI 10.1002/1521-3773(20000804)39:15<2748::AID-ANIE2748>3.0.CO
  • [12] 2-8
  • [13] Differential cross sections for H+D2→HD (v′=2, J′=0,3,5)+D at 1.55 eV
    Fernández-Alonso, F
    Bean, BD
    Zare, RN
    [J]. JOURNAL OF CHEMICAL PHYSICS, 1999, 111 (06) : 2490 - 2498
  • [14] New scheme for measuring the angular momentum spatial anisotropy of vibrationally excited H2 via the I 1Πg state
    Fernández-Alonso, F
    Bean, BD
    Ayers, JD
    Pomerantz, AE
    Zare, RN
    [J]. ZEITSCHRIFT FUR PHYSIKALISCHE CHEMIE-INTERNATIONAL JOURNAL OF RESEARCH IN PHYSICAL CHEMISTRY & CHEMICAL PHYSICS, 2000, 214 : 1167 - 1186
  • [15] FERNANDEZALONSO F, 1999, THESIS STANFORD U
  • [16] REDUCTION OF 1+1 RESONANCE ENHANCED MPI SPECTRA TO POPULATIONS AND ALIGNMENT FACTORS
    JACOBS, DC
    ZARE, RN
    [J]. JOURNAL OF CHEMICAL PHYSICS, 1986, 85 (10) : 5457 - 5468
  • [17] Kandel SA, 1997, CHEM PHYS LETT, V265, P121, DOI 10.1016/S0009-2614(96)01421-2
  • [18] Angular distributions for the Cl+C2H6→HCl+C2H5 reaction observed via multiphoton ionization of the C2H5 radical
    Kandel, SA
    Rakitzis, TP
    Lev-On, T
    Zare, RN
    [J]. JOURNAL OF PHYSICAL CHEMISTRY A, 1998, 102 (13) : 2270 - 2273
  • [19] Dynamics for the Cl+C2H6->HCl+C2H5 reaction examined through state-specific angular distributions
    Kandel, SA
    Rakitzis, TP
    LevOn, T
    Zare, RN
    [J]. JOURNAL OF CHEMICAL PHYSICS, 1996, 105 (17) : 7550 - 7559
  • [20] Cl + HD (v=1; J=1,2) reaction dynamics:: Comparison between theory and experiment
    Kandel, SA
    Alexander, AJ
    Kim, ZH
    Zare, RN
    Aoiz, FJ
    Bañares, L
    Castillo, JF
    Rábanos, VS
    [J]. JOURNAL OF CHEMICAL PHYSICS, 2000, 112 (02) : 670 - 685