Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/113941
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.contributorResearch Institute for Smart Energy-
dc.creatorWang, S-
dc.creatorZhou, J-
dc.creatorJin, J-
dc.creatorJiang, H-
dc.creatorMai, M-
dc.creatorDuan, L-
dc.creatorZhang, X-
dc.creatorWong, WY-
dc.date.accessioned2025-07-02T03:29:25Z-
dc.date.available2025-07-02T03:29:25Z-
dc.identifier.issn1944-8244-
dc.identifier.urihttp://hdl.handle.net/10397/113941-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.rightsCopyright © 2025 The Authors. Published by American Chemical Society. This publication is licensed under CC-BY 4.0 (https://creativecommons.org/licenses/by/4.0/).en_US
dc.rightsThe following publication Wang, S., Zhou, J., Jin, J., Jiang, H., Mai, M., Duan, L., ... & Wong, W. Y. (2025). Excited-State Engineering toward Accelerated Reverse Intersystem Crossing in Diindolocarbazole-Embedded Multiple-Resonance Emitters for High-Performance Blue OLEDs. ACS Applied Materials & Interfaces, 17(21), 31192-31200 is available at https://doi.org/10.1021/acsami.5c05420.en_US
dc.subjectBlue organic light-emitting diodesen_US
dc.subjectDiindolocarbazole-embedded multiple-resonance emittersen_US
dc.subjectExcited-state engineeringen_US
dc.subjectReverse intersystem crossingen_US
dc.subjectThermally activated delayed fluorescenceen_US
dc.titleExcited-state engineering toward accelerated reverse intersystem crossing in diindolocarbazole-embedded multiple-resonance emitters for high-performance blue OLEDsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage31192-
dc.identifier.epage31200-
dc.identifier.volume17-
dc.identifier.issue21-
dc.identifier.doi10.1021/acsami.5c05420-
dcterms.abstractSimultaneously achieving a narrow emission band, high efficiency, and excellent color purity remains a formidable challenge in the development of blue organic light-emitting diodes (OLEDs). Diindolocarbazole-embedded multiple-resonance emitters show great potential owing to their extremely narrow emission band, but the practical applications are severely limited by the slow reverse intersystem crossing rate (kRISC) with the order of magnitude value of 102. Herein, we present an effective strategy to accelerate the RISC process by acceptor decoration to regulate the excited state. Through modulating the electron-withdrawing ability from TFB to TPT, the long-range charge transfer excited state is successfully induced, which leads to the decreased ΔEST and increased spin-orbital coupling (SOC) matrix elements, contributing to the dramatically accelerated kRISC up to 1.11 × 104 s-1 for pICz-TPT. Moreover, the narrowband blue emission is basically retained for the proof-of-concept pICz-TPT with an emission peak at 449 nm, a full width at half-maximum of 44 nm, and CIE coordinates of (0.15, 0.10). Impressively, the nonsensitized OLEDs based on the pICz-TPT emitter exhibit the highest maximum external quantum efficiency (EQEmax) of 14.4% among all the reported blue OLEDs on the basis of pICz derivatives (which typically remained below 5%), and a further boost of efficiency with EQEmax of 24.2% is realized in the hyperfluorescent OLEDs. This work provides a powerful design tool toward highly efficient emitters with good color purity.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationACS Applied Materials and Interfaces, 28 May 2025, v. 17, no. 21, p. 31192-31200-
dcterms.isPartOfACS applied materials and interfaces-
dcterms.issued2025-05-28-
dc.identifier.scopus2-s2.0-105005216123-
dc.identifier.pmid40377905-
dc.identifier.eissn1944-8252-
dc.description.validate202507 bchy-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_TAen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Key R&D Program of China; ITC Guangdong-Hong Kong Technology Cooperation Funding Scheme (TCFS); CAS-Croucher Funding Scheme for Joint Laboratories; Endowed Professorship in Energy; Research Institute for Smart Energy (CDAQ); National Natural Science Foundation of China; Beijing Postdoctoral Research Foundation; National Natural Science Foundation of China; National Natural Science Foundation of Chinaen_US
dc.description.pubStatusPublisheden_US
dc.description.TAACS (2025)en_US
dc.description.oaCategoryTAen_US
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