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Organic thermally activated delayed fluorescence (TADF) compounds used in photocatalysis

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dc.contributor.authorBryden, Megan Amy
dc.contributor.authorZysman-Colman, Eli
dc.date.accessioned2021-05-19T11:30:08Z
dc.date.available2021-05-19T11:30:08Z
dc.date.issued2021-07-07
dc.identifier274184837
dc.identifier052f82cc-1f46-43ea-912b-4acd4c8d54fb
dc.identifier000651537800001
dc.identifier85109217494
dc.identifier.citationBryden , M A & Zysman-Colman , E 2021 , ' Organic thermally activated delayed fluorescence (TADF) compounds used in photocatalysis ' , Chemical Society Reviews , vol. 50 , no. 13 , pp. 7587-7680 . https://doi.org/10.1039/D1CS00198Aen
dc.identifier.issn0306-0012
dc.identifier.urihttps://hdl.handle.net/10023/23222
dc.descriptionWe thank Syngenta and the EPSRC Centre for Doctoral Training in Critical Resource Catalysis (CRITICAT) for financial support [Ph.D. studentship to “M.B.”; Grant code: EP/L016419/1].en
dc.description.abstractOrganic compounds that show Thermally Activated Delayed Fluorescence (TADF) have become wildly popular as next-generation emitters in organic light emitting diodes (OLEDs). Since 2016, a subset of these have found increasing use as photocatalysts. This review comprehensively highlights their potential by documenting the diversity of the reactions where an organic TADF photocatalyst can be used in lieu of a noble metal complex photocatalyst. Beyond the small number of TADF photocatalysts that have been used to date, the analysis conducted within this review reveals the wider potential of organic donor-acceptor TADF compounds as photocatalysts. A discussion of the benefits of compounds showing TADF for photocatalysis is presented, which paints a picture of a very promising future for organic photocatalyst development.
dc.format.extent94
dc.format.extent16259847
dc.language.isoeng
dc.relation.ispartofChemical Society Reviewsen
dc.subjectQD Chemistryen
dc.subjectT-NDASen
dc.subject.lccQDen
dc.titleOrganic thermally activated delayed fluorescence (TADF) compounds used in photocatalysisen
dc.typeJournal itemen
dc.contributor.sponsorEPSRCen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. Organic Semiconductor Centreen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doi10.1039/D1CS00198A
dc.description.statusPeer revieweden
dc.identifier.grantnumberEP/L016419/1en


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