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
来源
JOURNAL OF CHEMICAL PHYSICS | 1999年 / 111卷 / 06期
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 50 条
  • [1] Differential cross sections for H+D2→HD(v′=1, J′=1,5,8)+D at 1.7 eV
    Fernández-Alonso, F
    Bean, BD
    Zare, RN
    JOURNAL OF CHEMICAL PHYSICS, 1999, 111 (03): : 1035 - 1042
  • [2] State-resolved differential and integral cross sections for the reaction H+D2→HD(v′=3,j'=0-7)+D at 1.64 eV collision energy
    Bean, BD
    Ayers, JD
    Fernández-Alonso, F
    Zare, RN
    JOURNAL OF CHEMICAL PHYSICS, 2002, 116 (15): : 6634 - 6639
  • [3] Measurement of the HD(v′=2,J′=3) product differential cross section for the H+D2 exchange reaction at 1.55±0.05 eV using the photoloc technique
    Fernández-Alonso, F
    Bean, BD
    Zare, RN
    JOURNAL OF CHEMICAL PHYSICS, 1999, 111 (03): : 1022 - 1034
  • [4] Measurement of the cross section for H+D2→HD(v′=3,j′=0)+D as a function of angle and energy
    Ayers, JD
    Pomerantz, AE
    Fernández-Alonso, F
    Ausfelder, F
    Bean, BD
    Zare, RN
    JOURNAL OF CHEMICAL PHYSICS, 2003, 119 (09): : 4662 - 4670
  • [5] Energy dependence of forward scattering in the differential cross section of the H+D2→HD(v′=3,j'′=0)+D reaction
    Aoiz, FJ
    Bañares, L
    Castillo, JF
    Sokolovski, D
    JOURNAL OF CHEMICAL PHYSICS, 2002, 117 (06): : 2546 - 2556
  • [6] Corroboration of theory for H+D2→D+HD (v′=3, j′=0) reactive scattering dynamics
    Goldberg, Noah T.
    Zhang, Jianyang
    Miller, Daniel J.
    Zare, Richard N.
    JOURNAL OF PHYSICAL CHEMISTRY A, 2008, 112 (39): : 9266 - 9268
  • [7] On the existence of resonances in the H+D2→HD(v′=0,j′=7)+D reaction at collision energies 0.6-1.3 eV
    Aoiz, FJ
    Bañares, L
    Castillo, JF
    JOURNAL OF CHEMICAL PHYSICS, 2001, 114 (19): : 8237 - 8239
  • [8] Observation of predicted resonance structure in the H+D2→HD(v′=0,j′=7)+D reaction at a collision energy of 0.94 eV
    Kendrick, BK
    Jayasinghe, L
    Moser, S
    Auzinsh, M
    Shafer-Ray, N
    PHYSICAL REVIEW LETTERS, 2000, 84 (19) : 4325 - 4328
  • [9] Using quantum rotational polarization moments to describe the stereodynamics of the H+D2(v=0,j=0)→HD(v′,j′)+D reaction
    de Miranda, MP
    Clary, DC
    Castillo, JF
    Manolopoulos, DE
    JOURNAL OF CHEMICAL PHYSICS, 1998, 108 (08): : 3142 - 3153
  • [10] Differential cross sections for H + D2 → HD(v′=2, j′=0,3,6,9) + D at center-of-mass collision energies of 1.25, 1.61, and 1.97 eV
    Bartlett, Nate C. -M.
    Jankunas, Justin
    Goswami, Tapas
    Zare, Richard N.
    Bouakline, Foudhil
    Althorpe, Stuart C.
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2011, 13 (18) : 8175 - 8179