Time-resolved observation of interatomic excitation-energy transfer in argon dimers

The ultrafast transfer of excitation energy from one atom to its neighbor is observed in singly charged argon dimers in a time-resolved extreme ultraviolet (XUV)-pump IR-probe experiment. In the pump step, bound 3s-hole states in the dimer are populated by single XUV-photon ionization. The excitatio...

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Veröffentlicht in:The Journal of chemical physics 2017-03, Vol.146 (10), p.104305-104305
Hauptverfasser: Mizuno, Tomoya, Cörlin, Philipp, Miteva, Tsveta, Gokhberg, Kirill, Kuleff, Alexander, Cederbaum, Lorenz S., Pfeifer, Thomas, Fischer, Andreas, Moshammer, Robert
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Sprache:eng
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Zusammenfassung:The ultrafast transfer of excitation energy from one atom to its neighbor is observed in singly charged argon dimers in a time-resolved extreme ultraviolet (XUV)-pump IR-probe experiment. In the pump step, bound 3s-hole states in the dimer are populated by single XUV-photon ionization. The excitation-energy transfer at avoided crossings of the potential-energy curves leads to dissociation of the dimer, which is experimentally observed by further ionization with a time-delayed IR-probe pulse. From the measured pump-probe delay-dependent kinetic-energy release of coincident Ar+ + Ar+ ions, we conclude that the transfer of energy occurs on a time scale of about 800 fs . This mechanism represents a fast relaxation process below the energy threshold for interatomic Coulombic decay.
ISSN:0021-9606
1089-7690
DOI:10.1063/1.4978233