Charge-transfer processes in collisions of slow H+ ions with hydrocarbon molecules: CH4, C2H2, C2H6, and C3H8

Toshio Kusakabe, Kensuke Asahina, Akira Iida, Yuji Tanaka, Yan Li, Gerhard Hirsch, Robert J. Buenker, Mineo Kimura, Hiroyuki Tawara, and Yohta Nakai
Phys. Rev. A 62, 062715 – Published 14 November 2000
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Abstract

Charge-transfer processes in collisions of H+ ions with CH4, C2H2, C2H6, and C3H8 molecules have been studied based on joint experimental and theoretical approaches in the collision energy from 0.2 to 4.0 keV. In the present experiment, the initial growth rate method was employed for determination of cross sections, while in the present theory, the molecular orbital expansion method was utilized for CH4 and C2H2 molecules. Both experimental and theoretical results indicate that if one assumes vibrationally excited molecular ions (CH4+, C2H2+, C2H6+, and C3H8+) in the exit channel, then charge-transfer processes are sometimes found to become more favorable due to an accidental resonant condition. This is the clear indication of the role of vibrational excited states for charge transfer, and is found to be particularly so as the molecular size increases.

  • Received 3 January 2000

DOI:https://doi.org/10.1103/PhysRevA.62.062715

©2000 American Physical Society

Authors & Affiliations

Toshio Kusakabe, Kensuke Asahina, Akira Iida, and Yuji Tanaka

  • Department of Nuclear Engineering, Kinki University, Higashi-Osaka, Osaka 577-8502, Japan

Yan Li, Gerhard Hirsch*, Robert J. Buenker, and Mineo Kimura

  • Theoretische Chemie, Bergische Universität-Gesamthochschule Wuppertal, D-42097 Wuppertal, Germany

Hiroyuki Tawara

  • Department of Physics, Kansas State University, Manhattan, Kansas 66506-2601

Yohta Nakai

  • Atomic Energy Research Institute, Kinki University, Higashi-Osaka, Osaka 577-8502, Japan

  • *Deceased.
  • Permanent address: Graduate School of Science and Engineering, Yamaguchi University, Ube 755-8611, Japan.

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Vol. 62, Iss. 6 — December 2000

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