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Title: Dynamic modification of the fragmentation of CO{sup q+} excited states generated with high-order harmonics

Journal Article · · Physical Review. A
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  1. J. R. Macdonald Laboratory, Physics Department, Kansas State University, Manhattan, Kansas, 66506 (United States)
  2. Lawrence Berkeley National Laboratory, Berkeley, California 94720 (United States)
  3. Physics Department, American University of Sharjah, Sharjah (United Arab Emirates)
  4. Max-Planck Institute of Quantum Optics, Hans-Kopfermann-Strasse 1, D-85748, Garching (Germany)

The dynamic process of fragmentation of CO{sup q+} excited states is investigated using a pump-probe approach. EUV radiation (32-48 eV) generated by high-order harmonics was used to ionize and excite CO molecules and a time-delayed infrared (IR) pulse (800 nm) was used to influence the evolution of the dissociating multichannel wave packet. Two groups of states, separable experimentally by their kinetic-energy release (KER), are populated by the EUV and lead to C{sup +}-O{sup +} fragmentation: direct double ionization of the neutral molecule and fragmentation of the cation leading to C{sup +}-O*, followed by autoionization of O*. The IR pulse was found to modify the KER of the latter group in a delay-dependent way which is explained with a model calculation.

OSTI ID:
21450802
Journal Information:
Physical Review. A, Vol. 82, Issue 4; Other Information: DOI: 10.1103/PhysRevA.82.043410; (c) 2010 The American Physical Society; ISSN 1050-2947
Country of Publication:
United States
Language:
English