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Enhanced ionization of hydrogen molecular ions in an intense laser field via a multiphoton resonance

Source: Phys. Rev. A 81, 013408 (2010); doi:10.1103/PhysRevA.81.013408

Published 15 January 2010

PACS
  • 33.80.Rv
    Multiphoton ionization and excitation to highly excited states in molecules
  • 42.50.Hz
    Strong-field excitation of optical transitions in quantum systems; multiphoton processes; dynamic Stark shift
  • 34.50.Gb
    Electronic excitation and ionization of molecules
  • YEAR: 2010
PUBLICATION DATA
ISSN:
1553-9601 (online)
Publisher:
AIP is a member of CrossRef APS
Ying-Jun Jin,1 Xiao-Min Tong,1,2 and Nobuyuki Toshima1
1Institute of Materials Science, Graduate School of Pure and Applied Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8573, Japan
2Center for Computational Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8577, Japan

Multiphoton ionization of hydrogen molecular ions in a 480-nm intense laser field is investigated by solving the time-dependent Schrödinger equation numerically in prolate spheroidal coordinates. We discretize space on a generalized pseudospectral grid and propagate the electronic wave function using a second-order split-operator method. By including and excluding the 2psigmau state in the basis expansion, we confirm that the observed 10-eV peak in a recent experiment [Litvinyuk et al., New J. Phys. 10, 083011 (2008)] comes from the enhanced ionization via three-photon resonant excitation of the molecular ions. By folding the calculated ionization rates with the vibrational density distribution, the kinetic energy release spectra are obtained, which are in reasonable agreement with the experimental measurement. Furthermore, using this enhanced ionization, a pump-probe experiment is suggested to trace the vibrational wave packet. ©2010 The American Physical Society
History: Received 17 September 2009; published 15 January 2010
Permalink: http://link.aps.org/abstract/PRA/v81/e013408
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