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dc.contributor.authorShiu, Wen_US
dc.contributor.authorLin, JJen_US
dc.contributor.authorLiu, KPen_US
dc.contributor.authorWu, Men_US
dc.contributor.authorParker, DHen_US
dc.date.accessioned2014-12-08T15:39:53Z-
dc.date.available2014-12-08T15:39:53Z-
dc.date.issued2004-01-01en_US
dc.identifier.issn0021-9606en_US
dc.identifier.urihttp://dx.doi.org/10.1063/1.1629668en_US
dc.identifier.urihttp://hdl.handle.net/11536/27255-
dc.description.abstractThe velocity map ion imaging technique was applied to measure the reaction excitation function for the first time. It was found that the "raw" excitation function was significantly distorted by the density-to-flux transformation of the title reaction. Through a systematic investigation, possible reasons for such a dramatic effect are outlined. In addition, the state-resolved, pair-correlated excitation functions and branching ratios are presented. Effects of imperfect time slicing in the time-sliced velocity imaging technique in general are also discussed. (C) 2004 American Institute of Physics.en_US
dc.language.isoen_USen_US
dc.titleImaging the pair-correlated excitation function: The F+CH4 -> HF(v ')+CH3 (nu=0) reactionen_US
dc.typeArticleen_US
dc.identifier.doi10.1063/1.1629668en_US
dc.identifier.journalJOURNAL OF CHEMICAL PHYSICSen_US
dc.citation.volume120en_US
dc.citation.issue1en_US
dc.citation.spage117en_US
dc.citation.epage122en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000187577400016-
dc.citation.woscount70-
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