Mixed classical-quantum approach to excitation, ionization, and fragmentation of H2+ in intense laser fields

Mathias Uhlmann, Thomas Kunert, Frank Grossmann, and Rüdiger Schmidt
Phys. Rev. A 67, 013413 – Published 30 January 2003
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Abstract

A mixed-classical-quantum approach to describe laser-induced excitation, fragmentation and, in particular, ionization of one-electron molecular dimers is presented. Self-consistent equations of motion for the classical nuclear dynamics and the quantum-mechanical electronic evolution are derived. They are solved using a combined set of basis functions for the electronic wave function consisting of atomic orbitals and chainlike arranged Gaussians to account for a realistic description of the continuum dynamics of the ionized electron. For the molecular benchmark system H2+, the obtained results are in good agreement with those of full-quantum-mechanical calculations, which are available for relatively short laser pulses. For longer pulses, the present calculation signals a transient effect of molecular stabilization against fragmentation at corresponding (low) laser intensities.

  • Received 5 August 2002

DOI:https://doi.org/10.1103/PhysRevA.67.013413

©2003 American Physical Society

Authors & Affiliations

Mathias Uhlmann*, Thomas Kunert, Frank Grossmann, and Rüdiger Schmidt

  • Institut für Theoretische Physik, Technische Universität Dresden, 01062 Dresden, Germany

  • *Electronic address: mathias@theory.phy.tu-dresden.de

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Vol. 67, Iss. 1 — January 2003

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