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dc.contributor.authorHsu, Chun-Chihen_US
dc.contributor.authorWang, Yu-Tingen_US
dc.contributor.authorYabushita, Atsushien_US
dc.contributor.authorLuo, Chih-Weien_US
dc.contributor.authorHsiao, Yi-Nanen_US
dc.contributor.authorLin, Shivan-Hueien_US
dc.contributor.authorKobayashi, Takayoshien_US
dc.date.accessioned2014-12-08T15:20:42Z-
dc.date.available2014-12-08T15:20:42Z-
dc.date.issued2011-10-27en_US
dc.identifier.issn1089-5639en_US
dc.identifier.urihttp://dx.doi.org/10.1021/jp2051307en_US
dc.identifier.urihttp://hdl.handle.net/11536/14719-
dc.description.abstractAzoaromatic dyes have been extensively investigated over the past decade due to their potential use in a variety of optical devices that exploit their ultrafast photoisomerization processes. Among the azoaromatic dyes, Disperse Red 19 is a commercially available azobenzene nonlinear optical chromophore with a relatively high ground-state dipole moment. In the present study, we used ultrafast time-resolved spectroscopy to clarify the dynamics of a push-pull substituted azobenzene dye. Solution and film samples exhibited different ultrafast dynamics, indicating that the molecular environment affects the photoisomerization dynamics of the dye.en_US
dc.language.isoen_USen_US
dc.titleEnvironment-Dependent Ultrafast Photoisomerization Dynamics in Azo Dyeen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/jp2051307en_US
dc.identifier.journalJOURNAL OF PHYSICAL CHEMISTRY Aen_US
dc.citation.volume115en_US
dc.citation.issue42en_US
dc.citation.spage11508en_US
dc.citation.epage11514en_US
dc.contributor.department電子物理學系zh_TW
dc.contributor.departmentDepartment of Electrophysicsen_US
dc.identifier.wosnumberWOS:000296204500004-
dc.citation.woscount4-
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