期刊
JOURNAL OF CHEMICAL PHYSICS
卷 131, 期 4, 页码 -出版社
AMER INST PHYSICS
DOI: 10.1063/1.3183538
关键词
deuterium; ground states; hydrogen ions; ion-molecule reactions; potential energy surfaces; reaction kinetics theory; rotational states; rotational-vibrational states
资金
- Spanish MICIN
- CSIC [FIS2007-62006, AP2006-03740, CTQ2008-02578]
- Institut du Developpement des Ressources en Informatique Scientifique (IDRIS), Orsay, France
The H++D-2 -> HD+D+ reaction has been theoretically investigated by means of an exact quantum mechanical approach, a quasiclassical trajectory method, and two statistical methods based in the propagation of either wave functions or trajectories. The study addresses the possible changes on the overall dynamics of the title reaction when the D-2 diatom is rotationally excited to its v=0, j=1 state. In addition, the reactivity for the ground rotational state on two different potential energy surfaces (PESs), namely, the surface by Aguado [J. Chem. Phys. 112, 1240 (2000)] and the PES by Kamisaka [J. Chem. Phys. 116, 654 (2002)], is examined. Reaction probabilities and cross sections at 0.524 and 0.1 eV collision energies are calculated. The major differences with respect to the reaction initiated with D-2 in its ground rovibrational state are observed for the lowest collision energy E-c=0.1 eV. Differential cross sections have been found to depend to some extend on the PES employed. In addition, at E-c=0.1 eV further discrepancies in the total and rotational cross sections are noticeable.
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