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dc.contributor.authorHashimoto, Senaen_US
dc.contributor.authorYabushita, Atsushien_US
dc.contributor.authorKobayashi, Takayoshien_US
dc.contributor.authorIwakura, Izumien_US
dc.date.accessioned2017-04-21T06:55:37Z-
dc.date.available2017-04-21T06:55:37Z-
dc.date.issued2016-04-16en_US
dc.identifier.issn0009-2614en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.cplett.2016.02.053en_US
dc.identifier.urihttp://hdl.handle.net/11536/133656-
dc.description.abstractThe reduction of 7,7,8,8-tetracyanoquinodimethane (TCNQ) generates a pi radical anion, TCNQ(center dot-), that dimerizes in methanol solution. This dimer ([TCNQ](2-)(2)) exhibits a charge-transfer absorption peak at 620 nm and will disproportionate to give TCNQ and TCNQ(2-) in response to excitation within this charge transfer band. The present study examined the electronic dynamics of [TCNQ](2-)(2) disproportionation. The disproportionation was found to proceed in two steps. Electron transfer, representing the first step, occurred within the 10 fs pulse window, followed by the actual dissociation, within 350 fs. The emission lifetime of the singlet excited state of TCNQ(2-) was estimated to be 900 fs. (C) 2016 Elsevier B.V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.titleReal-time measurements of ultrafast electronic dynamics in the disproportionation of [TCNQ](2-)(2) using a visible sub-10 fs pulse laseren_US
dc.identifier.doi10.1016/j.cplett.2016.02.053en_US
dc.identifier.journalCHEMICAL PHYSICS LETTERSen_US
dc.citation.volume650en_US
dc.citation.spage47en_US
dc.citation.epage51en_US
dc.contributor.department電子物理學系zh_TW
dc.contributor.departmentDepartment of Electrophysicsen_US
dc.identifier.wosnumberWOS:000374966900009en_US
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