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Phys. Rev. A 74, 043416 (2006) [10 pages]

Detailed instantaneous ionization rate of H2+ in an intense laser field

Mohsen Vafaee,1 Hassan Sabzyan,1 Zahra Vafaee,2 and Ali Katanforoush3
1Department of Chemistry, University of Isfahan, Isfahan 81746-73441, I. R. Iran
2Department of Mathematics, University of Isfahan, Isfahan 81746-73441, I. R. Iran
3School of Mathematics, Institute for Studies in Theoretical Physics and Mathematics (IPM), Tehran 19395-5746, I. R. Iran

Received 10 June 2006; published 23 October 2006

Component instantaneous ionization rate (IIR) is introduced and the approach of its calculation is formulated. The component IIR's and the overall (time-averaged) component ionization rates are calculated for H2+ at different values of internuclear distance in a linearly polarized laser field with I=1.0×1014  W/cm2 intensity and lambda=1064  nm wavelength by direct numerical solution of the fixed-nuclei full dimensional time-dependent Schrödinger equation. The exact overall component ionization rates calculated by time-averaging of the component IIR are compared with those calculated approximately via the virtual detector (VD) method. Details of the time-dependent behavior of the outgoing and incoming electron wave packets of the H2+ system in intense laser field at subfemtosecond time scale are studied based on the calculated component IIR. It is shown clearly that the positive (outgoing electron wave packet) signals of the IIR and its z component are strong and sharp but the negative (returning electron wave packet) signals of the IIR are smooth and weak. The structure of the rho component of the IIR has smooth structure. Relation between the R-dependent ionization rate and duration of the ramp of the laser pulse is studied and it is explicitly shown that for internuclear distance R<5.6, when the laser pulse is turned on without a ramp, the first peak of R-dependent ionization rates moves towards the peak of the lower time-dependent Floquet quasienergy state (QES).

©2006 The American Physical Society

URL: http://link.aps.org/doi/10.1103/PhysRevA.74.043416
DOI: 10.1103/PhysRevA.74.043416
PACS: 33.80.Rv; 42.50.Hz; 42.65.Ky
  • 33.80.Rv
    Multiphoton ionization and excitation to highly excited states in molecules e.g., Rydberg states
  • 42.50.Hz
    Strong-field excitation of optical transitions in quantum systems; multiphoton processes; dynamic Stark shift
  • 42.65.Ky
    Optical frequency conversion; optical harmonic generation, including higher-order harmonic generation
  • YEAR: 2006
KEYWORDS: hydrogen ions, positive ions, molecule-photon collisions, photoionisation, Schrodinger equation

See Also

Comment on “Detailed instantaneous ionization rate of H2+ in an intense laser field”
Alejandro Saenz and Manohar Awasthi
Phys. Rev. A 76, 067401 (2007)

Reply to “Comment on `Detailed instantaneous ionization rate of H2+ in intense laser field' ”
Mohsen Vafaee and Hassan Sabzyan
Phys. Rev. A 76, 067402 (2007)

REFERENCES (29)

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Related Articles

  1. Comment on “Detailed instantaneous ionization rate of H2+ in an intense laser field”
    Alejandro Saenz and Manohar Awasthi
    Phys. Rev. A 76, 067401 (2007)
  2. Reply to “Comment on `Detailed instantaneous ionization rate of H2+ in intense laser field' ”
    Mohsen Vafaee and Hassan Sabzyan
    Phys. Rev. A 76, 067402 (2007)


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