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dc.contributor.authorWang, Yi-Hsiehen_US
dc.contributor.authorMineo, H.en_US
dc.contributor.authorChao, S. D.en_US
dc.contributor.authorSelzle, H. L.en_US
dc.contributor.authorNeusser, H. J.en_US
dc.contributor.authorSchlag, E. W.en_US
dc.contributor.authorTeranishi, Y.en_US
dc.contributor.authorLin, S. H.en_US
dc.date.accessioned2014-12-08T15:12:08Z-
dc.date.available2014-12-08T15:12:08Z-
dc.date.issued2011-02-14en_US
dc.identifier.issn0021-9606en_US
dc.identifier.urihttp://dx.doi.org/10.1063/1.3547363en_US
dc.identifier.urihttp://hdl.handle.net/11536/9306-
dc.description.abstractWe have theoretically studied important dynamic processes involved in zero electron kinetic energy (ZEKE) spectroscopy using the density matrix method with the inverse Born-Oppenheimer approximation basis sets. In ZEKE spectroscopy, the ZEKE Rydberg states are populated by laser excitation (either a one- or two- photon process), which is followed by autoionizations and l-mixing due to a stray field. The discrimination field is then applied to ionize loosely bound electrons in the ZEKE states. This is followed by using the extraction field to extract electrons from the ZEKE levels which have a strength comparable to that of the extraction field. These extracted electrons are measured for the relative intensities of the ion states under investigation. The spectral positions are determined by the applied laser wavelength and modified by the extraction electric field. In this paper, all of these processes are conducted within the context of the density matrix method. The density matrix method can provide not only the dynamics of system's population and coherence (or phase) but also the rate constants of the processes involved in the ZEKE spectroscopy. Numerical examples are given to demonstrate the theoretical treatments. (C) 2011 American Institute of Physics. [doi: 10.1063/1.3547363]en_US
dc.language.isoen_USen_US
dc.titleA master equation approach to the dynamics of zero electron kinetic energy (ZEKE) states and ZEKE spectroscopyen_US
dc.typeArticleen_US
dc.identifier.doi10.1063/1.3547363en_US
dc.identifier.journalJOURNAL OF CHEMICAL PHYSICSen_US
dc.citation.volume134en_US
dc.citation.issue6en_US
dc.citation.epageen_US
dc.contributor.department應用化學系分子科學碩博班zh_TW
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.identifier.wosnumberWOS:000287327400036-
dc.citation.woscount3-
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