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 |
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Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
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. |
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ISSN: | 0021-9606 1089-7690 |
DOI: | 10.1063/1.4978233 |