Differential cross sections for H+D2→HD (v′=2, J′=0,3,5)+D at 1.55 eV

被引:32
作者
Fernández-Alonso, F [1 ]
Bean, BD [1 ]
Zare, RN [1 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
关键词
D O I
10.1063/1.479527
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 photoloc technique with core extraction of the nascent product laboratory speed distribution in a Wiley-McLaren time-of-flight spectrometer has been used to measure differential cross sections for the reaction H+D-2--> HD (v(')=2, J(')=0,3,5)+D at collision energies similar to 1.55 eV. We find that the peak of each angular distribution shifts from complete backward scattering toward side scattering as the rotational excitation of the product increases. We found the same trend in our previous study of H+D-2--> HD (v(')=1, J(')=1,5,8)+D at similar to 1.70 eV. We conclude that the same type of correlation exists between impact parameter and rotational quantum number in both product vibrational manifolds. Further analysis of the HD (v(')=2, J(')) differential cross section data reveals, however, a clear tendency of this vibrational manifold to scatter sideways at lower J(') than HD(v(')=1, J(')). Within the framework of a line-of-centers model with nearly elastic specular scattering, this result implies that smaller impact parameters lead to more vibrationally excited products. (C) 1999 American Institute of Physics. [S0021-9606(99)01130-7].
引用
收藏
页码:2490 / 2498
页数:9
相关论文
共 60 条
  • [1] Stereodynamics of the reaction O(D-1(2))+H-2(upsilon=0)->OH(X-2 Pi(i);upsilon'=0,N',f)+H: State-resolved linear and rotational angular momentum distributions
    Alexander, AJ
    Aoiz, FJ
    Banares, L
    Brouard, M
    Short, J
    Simons, JP
    [J]. JOURNAL OF PHYSICAL CHEMISTRY A, 1997, 101 (41) : 7544 - 7557
  • [2] [Anonymous], 1986, NUMERICAL RECIPES FO
  • [3] QUANTUM-MECHANICAL AND QUASI-CLASSICAL CALCULATIONS FOR THE H+D-2-]HD+D REACTION - REACTION PROBABILITIES AND DIFFERENTIAL CROSS SECTIONS
    AOIZ, FJ
    BANARES, L
    DMELLO, MJ
    HERRERO, VJ
    RABANOS, VS
    SCHNIEDER, L
    WYATT, RE
    [J]. JOURNAL OF CHEMICAL PHYSICS, 1994, 101 (07) : 5781 - 5791
  • [4] Experimental and quantum mechanical study of the H+D2 reaction near 0.5 eV:: The assessment of the H3 potential energy surfaces
    Bañares, L
    Aoiz, FJ
    Herrero, VJ
    D'Mello, MJ
    Niederjohann, B
    Seekamp-Rahn, K
    Wrede, E
    Schnieder, L
    [J]. JOURNAL OF CHEMICAL PHYSICS, 1998, 108 (15) : 6160 - 6169
  • [5] THE H+D2 REACTION - QUASICLASSICAL SIMULATION OF NASCENT HD RO-VIBRATIONAL STATE DISTRIBUTIONS UNDER EXPERIMENTALLY PROBED HIGH-ENERGY CONDITIONS
    BLAIS, NC
    TRUHLAR, DG
    [J]. CHEMICAL PHYSICS LETTERS, 1989, 162 (06) : 503 - 510
  • [6] CALCULATED PRODUCT-STATE DISTRIBUTIONS FOR THE REACTION H+D2-]HD+D AT RELATIVE TRANSLATIONAL ENERGIES 0.55 AND 1.30 EV
    BLAIS, NC
    TRUHLAR, DG
    [J]. CHEMICAL PHYSICS LETTERS, 1983, 102 (2-3) : 120 - 125
  • [7] A refined H-3 potential energy surface
    Boothroyd, AI
    Keogh, WJ
    Martin, PG
    Peterson, MR
    [J]. JOURNAL OF CHEMICAL PHYSICS, 1996, 104 (18) : 7139 - 7152
  • [8] An experimental study of the dynamics of the reaction H+CO2→OH(v′,j′,f)+CO:: Product state-resolved differential cross sections and translational energy release distributions
    Brouard, M
    Hughes, DW
    Kalogerakis, KS
    Simons, JP
    [J]. JOURNAL OF PHYSICAL CHEMISTRY A, 1998, 102 (47) : 9559 - 9564
  • [9] H+H2 - THE CURRENT STATUS
    BUCHENAU, H
    TOENNIES, JP
    ARNOLD, J
    WOLFRUM, J
    [J]. BERICHTE DER BUNSEN-GESELLSCHAFT-PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1990, 94 (11): : 1231 - 1248
  • [10] STATE-RESOLVED DIFFERENTIAL CROSS-SECTIONS FOR THE REACTION D+H2-]HD+H
    BUNTIN, SA
    GIESE, CF
    GENTRY, WR
    [J]. JOURNAL OF CHEMICAL PHYSICS, 1987, 87 (02) : 1443 - 1445