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dc.contributor.authorWang, Q. Q.en_US
dc.contributor.authorMineo, H.en_US
dc.contributor.authorWu, D.en_US
dc.contributor.authorJin, M. X.en_US
dc.contributor.authorChin, C. H.en_US
dc.contributor.authorTeranishi, Y.en_US
dc.contributor.authorChao, S. D.en_US
dc.contributor.authorDing, D.en_US
dc.contributor.authorLin, S. H.en_US
dc.date.accessioned2014-12-08T15:09:02Z-
dc.date.available2014-12-08T15:09:02Z-
dc.date.issued2009-08-01en_US
dc.identifier.issn1054-660Xen_US
dc.identifier.urihttp://dx.doi.org/10.1134/S1054660X09150419en_US
dc.identifier.urihttp://hdl.handle.net/11536/6884-
dc.description.abstractThe mechanisms of ionization and dissociation of cyclohexanone (C(6)H(10)O) in a 90 fs, 788 nm linearly polarized laser field ranging from 10(13) to 10(14) W/cm(2) by a time-of-flight mass spectrometer (TOF-MS) have been investigated. The ion yields as a function of laser intensity have been measured experimentally. By comparison with the Ammosov-Delone-Krainov (ADK) theory based on a hydrogen-like model, the ionization mechanism of cyclohexanone in this intense femtosecond laser field has been understood. Considering the importance of molecular nuclear motions, we propose that the Franck-Condon (F-C) factor can provide the excess vibrational energy in the molecular ion. This energy is required for the decomposition of the molecular ion which finally results in the observed mass spectrum.en_US
dc.language.isoen_USen_US
dc.titleMolecular ionization of cyclohexanone in femtosecond laser fields: An application of ADK theoryen_US
dc.typeArticleen_US
dc.identifier.doi10.1134/S1054660X09150419en_US
dc.identifier.journalLASER PHYSICSen_US
dc.citation.volume19en_US
dc.citation.issue8en_US
dc.citation.spage1671en_US
dc.citation.epage1676en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000269012800029-
dc.citation.woscount0-
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