Published August 2010 | Version v1
Journal article

Radiative and nonradiative charge transfer in collisions of Be2+ and B3+ ions with H atoms

  • 1. Key Laboratory of Computational Physics, Institute of Applied Physics and Computational Mathematics, P.O. Box 8009, Beijing 100088 (China)
  • 2. College of Material Sciences and Optoelectronic Technology, Graduate University of the Chinese Academy of Sciences, P.O. Box 4588, Beijing 100049 (China)
  • 3. Institut fuer Energieforschung-Plasmaphysik, Forschungszentrum Juelich GmbH, EURATOM Association, Trilateral Euregio Cluster, D-52425 Juelich (Germany)
  • 4. Macedonian Academy of Sciences and Arts, P.O. Box 428, 1000 Skopje (Macedonia, The Former Yugoslav Republic of)

Description

The nonradiative charge-transfer processes in Be2+(1s2)+H(1s) and B3+(1s2)+H(1s) collisions are investigated by the quantal molecular orbital close-coupling method in the energy range of 10-5eV/u-10 keV/u and by the two-center atomic-orbital close-coupling method in the energy range of 0.1-100 keV/u. The radiative charge-transfer cross sections are calculated by using the optical potential and semiclassical methods in the energy range 10-5-100 eV/u. For both collision systems, the nonradiative charge-transfer cross sections in the low-energy region show an increasing behavior with decreasing energy. The nonradiative process is the dominant charge-transfer process in the Be2+(1s2)+H(1s) collision in the entire eV and sub-eV energy region. In the B3+(1s2)+H(1s) collision case, however, the cross section for radiative decay to 1 2Σ+ and 2 2Σ+ molecular states significantly exceeds that for the nonradiative process for energies below 30 eV/u.

Additional details

Identifiers

Publishing Information

Journal Title
Physical Review. A
Journal Volume
82
Journal Issue
2
Journal Page Range
p. 022710-022710.9
ISSN
1050-2947
CODEN
PLRAAN

Optional Information

Notes
(c) 2010 The American Physical Society