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dc.contributor.authorLiu, Tswen-Hsinen_US
dc.contributor.authorChen, Chin H.en_US
dc.date.accessioned2014-12-08T15:15:34Z-
dc.date.available2014-12-08T15:15:34Z-
dc.date.issued2006-11-01en_US
dc.identifier.issn0021-8979en_US
dc.identifier.urihttp://dx.doi.org/10.1063/1.2372570en_US
dc.identifier.urihttp://hdl.handle.net/11536/11649-
dc.description.abstractAn osmium(II) complex, Os(fptz)(2)(PPh2Me)(2) [fptz=3-trifluoromethyl-5-(2-pyridyl)-1,2,4-triazole, PPh2Me=methyl-diphenyl-phosphan], when doped in a 4,4(')-N,N-'-dicarbazolebiphenyl host as a phosphorescent red emitter in organic light-emitting devices, has the unusual property of resisting concentration quenching and sustaining its external quantum efficiency (EQE) (8%-9%) over a wide range of doping concentration (20%-40%). Single-crystal x-ray diffraction evidence is presented that the difference in doping behaviors can be linked to the octahedral configuration of Os(fptz)(2)(PPh2Me)(2), which could prevent the undesirable molecular aggregation from occurring at high concentration, thus delaying the onset of quenching. Accordingly, the high doping concentration of Os(fptz)(2)(PPh2Me)(2) leads to a significant suppression of luminescence quenching at high brightness/current and achieves a "flat" EQE versus brightness response owing to the increase in the emission sites in the emission layer. (c) 2006 American Institute of Physics.en_US
dc.language.isoen_USen_US
dc.titleOrganic light-emitting devices based on a highly robust osmium(II) complexen_US
dc.typeArticleen_US
dc.identifier.doi10.1063/1.2372570en_US
dc.identifier.journalJOURNAL OF APPLIED PHYSICSen_US
dc.citation.volume100en_US
dc.citation.issue9en_US
dc.citation.epageen_US
dc.contributor.department光電工程學系zh_TW
dc.contributor.departmentDepartment of Photonicsen_US
dc.identifier.wosnumberWOS:000242041500111-
dc.citation.woscount2-
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