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dc.contributor.authorSharifi, A.en_US
dc.contributor.authorKong, F.en_US
dc.contributor.authorChin, S. L.en_US
dc.contributor.authorMineo, H.en_US
dc.contributor.authorDyakov, Y.en_US
dc.contributor.authorMebel, A. M.en_US
dc.contributor.authorChao, S. D.en_US
dc.contributor.authorHayashi, M.en_US
dc.contributor.authorLin, S. H.en_US
dc.date.accessioned2014-12-08T15:13:20Z-
dc.date.available2014-12-08T15:13:20Z-
dc.date.issued2007-09-27en_US
dc.identifier.issn1089-5639en_US
dc.identifier.urihttp://dx.doi.org/10.1021/jp074053fen_US
dc.identifier.urihttp://hdl.handle.net/11536/10308-
dc.description.abstractThe main purpose of this paper is to report the high-power laser ionization-dissociation of CH4 at various femtosecond (fs) laser intensities (from 1 x 10 14 W/cm(2) to 2 x 1015 W/cm(2)) with a laser pulse duration of 48 fs. The generalized molecular Keldysh theory has been applied to calculate the ionization yields for CH4+ and CH4++. Outside the influence of the A intense laser, we propose to calculate the mass spectra due to the decomposition of CH4+ and CH4++, using the Rice-Ramsperger-Kassel-Marcus (RRKM) theory. The agreement between the experimental mass spectra and calculated mass spectra seems to be reasonable.en_US
dc.language.isoen_USen_US
dc.titleExperimental and theoretical investigation of high-power laser ionization and dissociation of methaneen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/jp074053fen_US
dc.identifier.journalJOURNAL OF PHYSICAL CHEMISTRY Aen_US
dc.citation.volume111en_US
dc.citation.issue38en_US
dc.citation.spage9405en_US
dc.citation.epage9416en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000249655600031-
dc.citation.woscount8-
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