Dynamic modification of the fragmentation of autoionizing states of O2+

W. Cao, G. Laurent, S. De, M. Schöffler, T. Jahnke, A. S. Alnaser, I. A. Bocharova, C. Stuck, D. Ray, M. F. Kling, I. Ben-Itzhak, Th. Weber, A. L. Landers, A. Belkacem, R. Dörner, A. E. Orel, T. N. Rescigno, and C. L. Cocke
Phys. Rev. A 84, 053406 – Published 10 November 2011

Abstract

The dynamic process of fragmentation of excited states of the molecular oxygen cation is investigated in a two-part study. First, using monochromatic 41.6 eV radiation and cold-target recoil-ion momentum spectroscopy detection of O+ + O+ ion pairs and associated electrons, we establish that this channel is populated only by an indirect process enabled by autoionization of excited oxygen atoms and identify the final active potential curves. Second, we probe the dynamics of this process using an attosecond pulse train of 35–42 eV EUV followed by an intense IR laser pulse. The results are compared with a model calculation.

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  • Received 13 September 2011

DOI:https://doi.org/10.1103/PhysRevA.84.053406

©2011 American Physical Society

Authors & Affiliations

W. Cao1, G. Laurent1, S. De1, M. Schöffler2, T. Jahnke3, A. S. Alnaser4, I. A. Bocharova2, C. Stuck3, D. Ray1, M. F. Kling1, I. Ben-Itzhak1, Th. Weber2, A. L. Landers5, A. Belkacem2, R. Dörner3, A. E. Orel6, T. N. Rescigno2, and C. L. Cocke1

  • 1J. R. Macdonald Laboratory, Department of Physics, Kansas State University, Manhattan, Kansas 66506, USA
  • 2Lawrence Berkeley National Laboratory, Chemical Sciences, Berkeley, California 94720, USA
  • 3Institut für Kernphysik, University of Frankfurt, D-60438 Frankfurt, Germany
  • 4Physics Department, American University of Sharjah, Sharjah, United Arab Emirates
  • 5Department of Physics, Auburn University, Auburn, Alabama 36849, USA
  • 6Department of Applied Science, University of California, Davis, California 95616, USA

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Issue

Vol. 84, Iss. 5 — November 2011

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