Journal
PHYSICAL REVIEW A
Volume 84, Issue 6, Pages -Publisher
AMER PHYSICAL SOC
DOI: 10.1103/PhysRevA.84.063412
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Funding
- Nederlandse organisatie voor Wetenschappelijk Onderzoek (NWO)
- Swedish Research Council
- Grants-in-Aid for Scientific Research [21350005] Funding Source: KAKEN
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We demonstrate that dissociative ionization of O-2 can be controlled by the relative delay between an attosecond pulse train (APT) and a copropagating infrared (IR) field. Our experiments reveal a dependence of both the branching ratios between a range of electronic states and the fragment angular distributions on the extreme ultraviolet (XUV) to IR time delay. The observations go beyond adiabatic propagation of dissociative wave packets on IR-induced quasistatic potential energy curves and are understood in terms of an IR-induced coupling between electronic states in the molecular ion.
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