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dc.rights.licenseopenen_US
dc.contributor.authorFRANCA, Larissa G.
dc.contributor.authorDOS SANTOS, Paloma L.
dc.contributor.authorPANDER, Piotr
hal.structure.identifierCentre de Recherche Paul Pascal [CRPP]
dc.contributor.authorCABRAL, Marília G. B.
dc.contributor.authorCRISTIANO, Rodrigo
dc.contributor.authorCAZATI, Thiago
dc.contributor.authorMONKMAN, Andrew P.
hal.structure.identifierCentre de Recherche Paul Pascal [CRPP]
dc.contributor.authorBOCK, Harald
dc.contributor.authorECCHER, Juliana
dc.date.accessioned2022-11-22T08:26:45Z
dc.date.available2022-11-22T08:26:45Z
dc.date.issued2022-06-27
dc.identifier.urioai:crossref.org:10.1021/acsaelm.2c00432
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/170337
dc.description.abstractEnDelayed fluorescence (DF) by triplet–triplet annihilation (TTA) is observed in solutions of a benzoperylene-imidoester mesogen that shows a hexagonal columnar mesophase at room temperature in the neat state. A similar benzoperylene-imide with a slightly smaller HOMO–LUMO gap, that also is hexagonal columnar liquid crystalline at room temperature, does not show DF in solution, and mixtures of the two mesogens show no DF in solution either, because of collisional quenching of the excited triplet states on the imidoester by the imide. In contrast, DF by TTA from the imide but not from the imidoester is observed in condensed films of such mixtures, even though neat films of either single material are not displaying DF. In contrast to the DF from the monomeric imidoester in solution, DF of the imide occurs from dimeric aggregates in the blend films, assisted by the imidoester. Thus, the close contact of intimately stacked molecules of the two different species in the columnar mesophase leads to a unique mesophase-assisted aggregate DF. This constitutes the first observation of DF by TTA from the columnar liquid crystalline state. If the imide is dispersed in films of polybromostyrene, which provides an external heavy-atom effect facilitating triplet formation, DF is also observed. Organic light-emitting diodes (OLEDs) devices incorporating these liquid crystal molecules demonstrated high external quantum efficiency (EQE). On the basis of the literature and to the best of our knowledge, the EQE reported is the highest among nondoped solution-processed OLED devices using a columnar liquid crystal molecule as the emitting layer.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.sourcecrossref
dc.subject.encolumnar liquid crystals
dc.subject.enoptical spectroscopy
dc.subject.entriplet−triplet annihilation
dc.subject.endelayed fluorescence
dc.subject.ensolution-processed OLED
dc.title.enDelayed Fluorescence by Triplet–Triplet Annihilation from Columnar Liquid Crystal Films
dc.typeArticle de revueen_US
dc.identifier.doi10.1021/acsaelm.2c00432en_US
dc.subject.halChimie/Matériauxen_US
bordeaux.journalACS Applied Electronic Materialsen_US
bordeaux.page3486-3494en_US
bordeaux.volume4en_US
bordeaux.hal.laboratoriesCentre de Recherche Paul Pascal (CRPP) - UMR 5031en_US
bordeaux.issue7en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionCNRSen_US
bordeaux.teamMatériaux moléculaires et magnétisme (M3)en_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.identifier.funderIDHorizon 2020en_US
bordeaux.import.sourcedissemin
hal.exportfalse
workflow.import.sourcedissemin
dc.rights.ccCC BYen_US
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