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
收藏
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 [J].
Fernández-Alonso, F ;
Bean, BD ;
Zare, RN .
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 [J].
Fernández-Alonso, F ;
Bean, BD ;
Ayers, JD ;
Pomerantz, AE ;
Zare, RN .
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 [J].
JACOBS, DC ;
ZARE, RN .
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 [J].
Kandel, SA ;
Rakitzis, TP ;
Lev-On, T ;
Zare, RN .
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 [J].
Kandel, SA ;
Rakitzis, TP ;
LevOn, T ;
Zare, RN .
JOURNAL OF CHEMICAL PHYSICS, 1996, 105 (17) :7550-7559
[20]   Cl + HD (v=1; J=1,2) reaction dynamics:: Comparison between theory and experiment [J].
Kandel, SA ;
Alexander, AJ ;
Kim, ZH ;
Zare, RN ;
Aoiz, FJ ;
Bañares, L ;
Castillo, JF ;
Rábanos, VS .
JOURNAL OF CHEMICAL PHYSICS, 2000, 112 (02) :670-685