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Phys. Rev. A 74, 033415 (2006) [6 pages]

Imaging electron molecular orbitals via ionization by intense femtosecond pulses

G. Lagmago Kamta and A. D. Bandrauk
Département de Chimie, Université de Sherbrooke, Sherbrooke, Québec, Canada J1K 2R1
Received 2 June 2006; published 28 September 2006

We report an ab initio investigation of the ionization of an oriented molecule (H2+) by intense linearly polarized laser pulses, using initial states (i.e., the active orbitals) having various symmetries and electron distributions. We show that the orientation dependence of the total (nondifferential) ionization probability of a molecule is very sensitive to the electron distribution within the active orbital. This sensitivity is strong enough that by collecting the ionization probability for various molecular orientations relative to the laser polarization, one can infer the electron distribution within the active orbital. The ionization of oriented molecules by intense low frequency fields can be a tool for imaging electron densities in active molecular orbitals.

©2006 The American Physical Society

URL: http://link.aps.org/doi/10.1103/PhysRevA.74.033415
DOI: 10.1103/PhysRevA.74.033415
PACS: 33.80.Rv; 33.80.Wz; 33.80.Eh; 42.50.Hz
  • 33.80.Rv
    Multiphoton ionization and excitation to highly excited states in molecules e.g., Rydberg states
  • 33.80.Wz
    Other multiphoton processes in molecules
  • 33.80.Eh
    Autoionization, photoionization, and photodetachment of molecules
  • 42.50.Hz
    Strong-field excitation of optical transitions in quantum systems; multiphoton processes; dynamic Stark shift
  • YEAR: 2006
KEYWORDS: positive ions, hydrogen ions, ab initio calculations, high-speed optical techniques, photoionisation, molecule-photon collisions

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