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dc.contributor.authorTsuchiya, Youichi
dc.contributor.authorDiesing, Stefan
dc.contributor.authorBencheikh, Fatima
dc.contributor.authorWada, Yoshimasa
dc.contributor.authordos Santos, Paloma L.
dc.contributor.authorKaji, Hironori
dc.contributor.authorZysman-Colman, Eli
dc.contributor.authorSamuel, Ifor D. W.
dc.contributor.authorAdachi, Chihaya
dc.date.accessioned2022-09-01T23:49:20Z
dc.date.available2022-09-01T23:49:20Z
dc.date.issued2021-09-02
dc.identifier275240368
dc.identifierabb68325-0af3-4970-927a-0b262f936751
dc.identifier85114893105
dc.identifier000697333300028
dc.identifier.citationTsuchiya , Y , Diesing , S , Bencheikh , F , Wada , Y , dos Santos , P L , Kaji , H , Zysman-Colman , E , Samuel , I D W & Adachi , C 2021 , ' Exact solution of kinetic analysis for thermally activated delayed fluorescence materials ' , Journal of Physical Chemistry A , vol. Articles ASAP . https://doi.org/10.1021/acs.jpca.1c04056en
dc.identifier.issn1089-5639
dc.identifier.otherORCID: /0000-0001-7183-6022/work/99466306
dc.identifier.urihttps://hdl.handle.net/10023/25935
dc.descriptionResearch at Kyushu, Kyoto and St Andrews Universities was supported by EPSRC and JSPS Core to Core grants (JSPS Core-to-core Program; EPSRC grant number EP/R035164/1). Authors are also grateful for financial support from the Program for Building Regional Innovation Ecosystems of the Ministry of Education, Culture, Sports, Science and Technology, Japan, JST ERATO Grant JPMJER1305, JSPS KAKENHI JP20H05840, and Kyulux Inc.en
dc.description.abstractThe photophysical analysis of thermally activated delayed fluorescence (TADF) materials has become instrumental to providing insight into their stability and performance, which is not only relevant for organic light-emitting diodes (OLED), but also for other applications such as sensing, imaging and photocatalysis. Thus, a deeper understanding of the photophysics underpinning the TADF mechanism is required to push materials design further. Previously reported analyses in the literature of the kinetics of the various processes occurring in a TADF material rely on several a priori assumptions to estimate the rate constants for forward and reverse intersystem crossing (ISC and RISC, respectively). In this report, we demonstrate a method to determine these rate constants using a three-state model together with a steady-state approximation and, importantly, no additional assumptions. Further, we derive the exact rate equations, greatly facilitating a comparison of the TADF properties of structurally diverse emitters and providing a comprehensive understanding of the photophysics of these systems.
dc.format.extent1526223
dc.format.extent425927
dc.language.isoeng
dc.relation.ispartofJournal of Physical Chemistry Aen
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titleExact solution of kinetic analysis for thermally activated delayed fluorescence materialsen
dc.typeJournal articleen
dc.contributor.sponsorEPSRCen
dc.contributor.institutionUniversity of St Andrews. School of Physics and Astronomyen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.contributor.institutionUniversity of St Andrews. Organic Semiconductor Centreen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. Centre for Biophotonicsen
dc.contributor.institutionUniversity of St Andrews. Condensed Matter Physicsen
dc.identifier.doi10.1021/acs.jpca.1c04056
dc.description.statusPeer revieweden
dc.date.embargoedUntil2022-09-02
dc.identifier.urlhttp://dx.doi.org/10.26434/chemrxiv.14178113.v1en
dc.identifier.grantnumberEP/R035164/1en


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