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dc.contributor.authorMehata, Mohan Singhen_US
dc.contributor.authorHsu, Chain-Shuen_US
dc.contributor.authorLee, Yuan-Pernen_US
dc.contributor.authorOhta, Nobuhiroen_US
dc.date.accessioned2019-04-02T05:58:14Z-
dc.date.available2019-04-02T05:58:14Z-
dc.date.issued2012-07-19en_US
dc.identifier.issn1932-7447en_US
dc.identifier.urihttp://dx.doi.org/10.1021/jp302666fen_US
dc.identifier.urihttp://hdl.handle.net/11536/150462-
dc.description.abstractElectric-field-induced changes of the absorption, photoluminescence, and photoluminescence excitation spectra and the photoluminescence decay profile have been measured for poly(2,3-diphenyl-5-hexyl-p-phenylene vinylene). The magnitudes of the change of electric dipole moment and molecular polarizability of this compound have been determined for excitation into the first excited state having a strong absorption, and a large charge-separated character, which is relevant for photovoltaic devices, is confirmed. The photoluminescence of this compound is quenched by application of an electric field, and the quenching efficiency increases with decreasing excitation wavelength. Field-assisted dissociation is considered to occur from the photoexcited Franck-Condon state, resulting in the field-induced decrease in the population of the emitting state, which induce the quenching of photoluminescence.en_US
dc.language.isoen_USen_US
dc.titleElectroabsorption and Electrophotoluminescence of Poly(2,3-diphenyl-5-hexyl-p-phenylene vinylene)en_US
dc.typeArticleen_US
dc.identifier.doi10.1021/jp302666fen_US
dc.identifier.journalJOURNAL OF PHYSICAL CHEMISTRY Cen_US
dc.citation.volume116en_US
dc.citation.spage14789en_US
dc.citation.epage14795en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.department應用化學系分子科學碩博班zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.identifier.wosnumberWOS:000306503200007en_US
dc.citation.woscount7en_US
Appears in Collections:Articles