4.7 Article

Near-resonant rotational energy transfer in HCl-H2 inelastic collisions

Journal

JOURNAL OF CHEMICAL PHYSICS
Volume 140, Issue 6, Pages -

Publisher

AMER INST PHYSICS
DOI: 10.1063/1.4864359

Keywords

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Funding

  1. Agence Nationale de la Recherche (ANR-HYDRIDES) [ANR-12-BS05-0011-01]
  2. CNRS national program Physique et Chimie du Milieu Interstellaire

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We present a new four-dimensional (4D) potential energy surface for the HCl-H-2 van der Waals system. Both molecules were treated as rigid rotors. Potential energy surface was obtained from electronic structure calculations using a coupled cluster with single, double, and perturbative triple excitations method. The four atoms were described using the augmented correlation-consistent quadruple zeta basis set and bond functions were placed at mid-distance between the HCl and H-2 centers of mass for a better description of the van der Waals interaction. The global minimum is characterized by the well depth of 213.38 cm (1) corresponding to the T-shape structure with H-2 molecule on the H side of the HCl molecule. The dissociation energies D-0 are 34.7 cm (1) and 42.3 cm(-1) for the complex with para-and ortho-H-2, respectively. These theoretical results obtained using our new PES are in good agreement with experimental values [D. T. Anderson, M. Schuder, and D. J. Nesbitt, Chem. Phys. 239, 253 (1998)]. Close coupling calculations of the inelastic integral rotational cross sections of HCl in collisions with para-H-2 and ortho-H-2 were performed at low and intermediate collisional energies. Significant differences exist between para-and ortho-H-2 results. The strongest collision-induced rotational HCl transitions are the transitions with Delta j = 1 for collisions with both para-H-2 and ortho-H-2. Rotational relaxation of HCl in collision with para-H-2 in the rotationally excited states j = 2 is dominated by near-resonant energy transfer. (C) 2014 AIP Publishing LLC.

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