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hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies
dc.contributor.authorDIMAMAY, Mariel
hal.structure.identifierTech Univ Darmstadt, Inst Mat Sci
dc.contributor.authorMAYER, Thomas
hal.structure.identifierLaboratoire de Chimie des Polymères Organiques [LCPO]
hal.structure.identifierTeam 4 LCPO : Polymer Materials for Electronic, Energy, Information and Communication Technologies
dc.contributor.authorHADZIIOANNOU, Georges
hal.structure.identifierTech Univ Darmstadt, Inst Mat Sci
dc.contributor.authorJAEGERMANN, Wolfram
dc.date.accessioned2020
dc.date.available2020
dc.date.issued2015
dc.identifier.issn0021-8979
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/20271
dc.description.abstractEnLuminescent organic phases embedded in conductive inorganic matrices are proposed for hybrid organic-inorganic light-emitting diodes. In this configuration, the organic dye acts as the radiative recombination site for charge carriers injected into the inorganic matrix. Our investigation is aimed at finding a material combination where the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) of the organic dye are situated in between the valence and conduction bands of the inorganic matrix in order to promote electron and hole transfer from the matrix to the dye. Bilayer and composite thin films of zinc selenide (ZnSe) and a red iridium complex (Ir(BPA)) organic light emitter were prepared in situ via UHV thermal evaporation technique. The electronic and atomic structures were studied applying X-ray and ultraviolet photoelectron spectroscopies. The measured energy band alignments for the ZnSe/Ir(BPA) bilayer and ZnSe+Ir(BPA) composite reveal that the HOMO and LUMO of the organic dye are positioned in the ZnSe bandgap. For the initial steps of ZnSe deposition on a dye film to form Ir(BPA)/ZnSe bilayers, zinc atoms intercalate into the dye film leaving behind an excess of selenium at the interface that partly reacts with dye molecules. Photoelectron spectroscopy of the composites shows the same species suggesting a similar mechanism. This mechanism leads to composite films with increased content of amorphous phases in the inorganic matrix, thereby affecting its conductivity, as well as to the presence of nonradiative recombination sites provided by the intercalated Zn atoms. (C) 2015 AIP Publishing LLC.
dc.language.isoen
dc.publisherAmerican Institute of Physics
dc.subject.enMOLECULES
dc.subject.enLASER-DIODES
dc.subject.enVACUUM LEVEL
dc.subject.enDEVICES
dc.subject.enEFFICIENCY
dc.subject.enENERGY-LEVEL ALIGNMENT
dc.subject.enTHIN-FILMS
dc.subject.enINTERFACE FORMATION
dc.subject.enIRIDIUM COMPLEXES
dc.subject.enQUANTUM DOTS
dc.title.enElectronic and chemical structure of an organic light emitter embedded in an inorganic wide-bandgap semiconductor: Photoelectron spectroscopy of layered and composite structures of Ir(BPA) and ZnSe
dc.typeArticle de revue
dc.identifier.doi10.1063/1.4919828
dc.subject.halChimie/Polymères
bordeaux.journalJournal of Applied Physics
bordeaux.pageArt Nb 175501
bordeaux.volume117
bordeaux.hal.laboratoriesLaboratoire de Chimie des Polymères Organiques (LCPO) - UMR 5629*
bordeaux.issue17
bordeaux.institutionBordeaux INP
bordeaux.institutionUniversité de Bordeaux
bordeaux.peerReviewedoui
hal.identifierhal-01361340
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-01361340v1
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