Published May 2010 | Version v1
Journal article

Isotope effects on the charge transfer into the n=1, 2, and 3 shells of He2+ in collisions with H, D, and T

  • 1. Helmholtz-Zentrum Berlin, Glienickerstrasse 100, D-14109 Berlin (Germany)
  • 2. Quantum Theory Project, Departments of Physics and Chemistry, University of Florida, Gainesville, Florida 32611-8435 (United States)
  • 3. Instituto de Ciencias Fisicas, Universidad Nacional Autonoma de Mexico, Apartado Postal 48-3, Cuernavaca, Morelos 62251 (Mexico)
  • 4. Physics Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831 (United States)
  • 5. KVI Atomic Physics, University of Groningen, NL-9747 AA Groningen (Netherlands)

Description

Processes for charge transfer into He2+ colliding with the atomic isotopes hydrogen (H), deuterium (D), and tritium (T) are theoretically studied at collision energies as low as 30 eV/amu. Probabilities and cross sections for electron capture into different shells of the projectile are calculated using an ab initio approach which solves the time-dependent Schroedinger equation. The results are interpreted in terms of radial and rotational couplings between molecular orbitals. The probabilities exhibit strong Stueckelberg oscillations for charge transfer into shells with the principal quantum numbers n=2 and 3 due to radial coupling mechanisms in specific ranges of the impact parameter. The total cross sections for charge transfer, evaluated for a given shell, differ by orders of magnitude, as different isotopes are used in the collisions. The isotope effect increases significantly for decreasing n=3, 2, and 1. This finding is attributed to the influence of the rotational coupling mechanism, which is strongly affected by the distance of closest approach between the collision partners.

Additional details

Identifiers

Publishing Information

Journal Title
Physical Review. A
Journal Volume
81
Journal Issue
5
Journal Page Range
p. 052704-052704.10
ISSN
1050-2947
CODEN
PLRAAN

Optional Information

Notes
(c) 2010 The American Physical Society