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[2.2]Paracyclophane-substituted chiral multiresonant thermally activated delayed fluorescence emitters for efficient organic light-emitting diodes
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dc.contributor.author | Xu, Yan | |
dc.contributor.author | Hafeez, Hassan | |
dc.contributor.author | Seibert, Jasmin | |
dc.contributor.author | Wu, Sen | |
dc.contributor.author | Ortiz, Jhon Sebastian Oviedo | |
dc.contributor.author | Crassous, Jeanne | |
dc.contributor.author | Bräse, Stefan | |
dc.contributor.author | Samuel, Ifor D. W. | |
dc.contributor.author | Zysman-Colman, Eli | |
dc.date.accessioned | 2024-03-21T10:30:02Z | |
dc.date.available | 2024-03-21T10:30:02Z | |
dc.date.issued | 2024-03-21 | |
dc.identifier | 300147363 | |
dc.identifier | 3bc69b59-ec30-438a-9b5f-7e2ade529b40 | |
dc.identifier | 85188188933 | |
dc.identifier.citation | Xu , Y , Hafeez , H , Seibert , J , Wu , S , Ortiz , J S O , Crassous , J , Bräse , S , Samuel , I D W & Zysman-Colman , E 2024 , ' [2.2]Paracyclophane-substituted chiral multiresonant thermally activated delayed fluorescence emitters for efficient organic light-emitting diodes ' , Advanced Functional Materials , vol. Early View . https://doi.org/10.1002/adfm.202402036 | en |
dc.identifier.issn | 1616-301X | |
dc.identifier.other | ORCID: /0000-0001-7183-6022/work/156133751 | |
dc.identifier.uri | https://hdl.handle.net/10023/29542 | |
dc.description | The authors aregrateful to the EPSRC for financial support (grant EP/W0151371/1and EP/W007517/1). Y.X. thanks the China Scholarship Council(202106310038) for support. J.S. thanks the Jürgen Manchot Foundation, the Karlsruhe School of Optics and Photonics, and Dr. Erik Strandberg and Bianca Posselt, for their help in ECD measurements.The authors thank the European Commission Research ExecutiveAgency (Grant Agreement number: 101073045−TADFsolutions−HORIZON-MSCA-2021-DN) and the EPSRC (EP/X026175/1) for financial support. The authors acknowledge the Ministère de l’EnseignementSupérieur et de la Recherche and the Centre National de la RechercheScientifique (CNRS). | en |
dc.description.abstract | The study reports two pairs of chiral multi-resonant thermally activated delayed fluorescence (MR-TADF) materials PCP-DiKTa and Czp-DiKTa by decorating a known MR-TADF core, DiKTa, with different [2.2]paracyclophane (PCP) based planar chiral groups. PCP-DiKTa shows narrow sky-blue emission with a full width at half maximum (FWHM) of 44 nm, while the emission of Czp-DiKTa is slightly broader with a FWHM of 66 nm and redshifted. Both emitters show high photoluminescence quantum yields of 93 and 99% for PCP-DiKTa and Czp-DiKTa, respectively. Enantiomerically pure samples of both compounds show chiroptical properties in the ground state while only Czp-DiKTa exhibits chiroptical activity in the excited state, with dissymmetry factors (|gPL|) of 4 × 10−4. Organic light-emitting diodes (OLEDs) with PCP-DiKTa and Czp-DiKTa show maximum external quantum efficiencies (EQEmax) of 25.7 and 29.2%, with λEL of 489 and 518 nm, and FWHMs of 53 and 69 nm, respectively. These EQEmax values are higher than those of other reported devices employing PCP-based D-A type emitters. This work demonstrates that the PCP moiety is not only a powerful building block to develop planar chiral emitters but one that is compatible with the fabrication of high efficiency devices. | |
dc.format.extent | 9 | |
dc.format.extent | 4470720 | |
dc.language.iso | eng | |
dc.relation.ispartof | Advanced Functional Materials | en |
dc.subject | [2.2]Paracyclophane | en |
dc.subject | Circularly polarized luminescence | en |
dc.subject | Multiresonant thermally activated delayed fluorescence | en |
dc.subject | Organic light-emitting diodes | en |
dc.subject | QD Chemistry | en |
dc.subject | DAS | en |
dc.subject.lcc | QD | en |
dc.title | [2.2]Paracyclophane-substituted chiral multiresonant thermally activated delayed fluorescence emitters for efficient organic light-emitting diodes | en |
dc.type | Journal article | en |
dc.contributor.sponsor | UKRI (EU) | en |
dc.contributor.sponsor | UK Research and Innovation | en |
dc.contributor.institution | University of St Andrews. School of Chemistry | en |
dc.contributor.institution | University of St Andrews. School of Physics and Astronomy | en |
dc.contributor.institution | University of St Andrews. Centre for Biophotonics | en |
dc.contributor.institution | University of St Andrews. Condensed Matter Physics | en |
dc.contributor.institution | University of St Andrews. Organic Semiconductor Centre | en |
dc.contributor.institution | University of St Andrews. Centre for Energy Ethics | en |
dc.contributor.institution | University of St Andrews. EaSTCHEM | en |
dc.identifier.doi | https://doi.org/10.1002/adfm.202402036 | |
dc.description.status | Peer reviewed | en |
dc.identifier.url | https://doi.org/10.26434/chemrxiv-2024-ds8tw | en |
dc.identifier.grantnumber | EP/X026175/1 | en |
dc.identifier.grantnumber | EP/W007517/1 | en |
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