David Hall
Diindolocarbazole – achieving multiresonant thermally activated delayed fluorescence without the need for acceptor units
Hall, David; Stavrou, Kleitos; Duda, Eimantas; Danos, Andrew; Bagnich, Sergey; Warriner, Stuart; Slawin, Alexandra M.Z.; Beljonne, David; Köhler, Anna; Monkman, Andrew; Olivier, Yoann; Zysman-Colman, Eli
Authors
Kleitos Stavrou kleitos.stavrou@durham.ac.uk
PGR Student Doctor of Philosophy
Eimantas Duda
Dr Andrew Danos andrew.danos@durham.ac.uk
Senior Experimental Officer
Sergey Bagnich
Stuart Warriner
Alexandra M.Z. Slawin
David Beljonne
Anna Köhler
Professor Andrew Monkman a.p.monkman@durham.ac.uk
Professor
Yoann Olivier
Eli Zysman-Colman
Abstract
In this work we present a new multi-resonance thermally activated delayed fluorescence (MR-TADF) emitter paradigm, demonstrating that the structure need not require the presence of acceptor atoms. Based on an in silico design, the compound DiICzMes4 possesses a red-shifted emission, enhanced photoluminescence quantum yield, and smaller singlet-triplet energy gap, ΔEST, than the parent indolocarbazole that induces MR-TADF properties. Coupled cluster calculations accurately predict the magnitude of the ΔEST when the optimized singlet and triplet geometries are used. Slow yet optically detectable reverse intersystem crossing contributes to low efficiency in organic light-emitting diodes using DiICzMes4 as the emitter. However, when used as a terminal emitter in combination with a TADF assistant dopant within a hyperfluorescence device architecture, maximum external quantum efficiencies of up to 16.5% were achieved at CIE (0.15, 0.11). This represents one of the bluest hyperfluorescent devices reported to date. Simultaneously, recognising that MR-TADF emitters do not require acceptor atoms reveals an unexplored frontier in materials design, where yet greater performance may yet be discovered.
Citation
Hall, D., Stavrou, K., Duda, E., Danos, A., Bagnich, S., Warriner, S., Slawin, A. M., Beljonne, D., Köhler, A., Monkman, A., Olivier, Y., & Zysman-Colman, E. (2022). Diindolocarbazole – achieving multiresonant thermally activated delayed fluorescence without the need for acceptor units. Materials Horizons, 9(3), 1068-1080. https://doi.org/10.1039/d1mh01383a
Journal Article Type | Article |
---|---|
Acceptance Date | Dec 16, 2021 |
Online Publication Date | Jan 24, 2022 |
Publication Date | Mar 1, 2022 |
Deposit Date | Feb 18, 2022 |
Publicly Available Date | Feb 18, 2022 |
Journal | Materials Horizons |
Electronic ISSN | 2051-6355 |
Publisher | Royal Society of Chemistry |
Peer Reviewed | Peer Reviewed |
Volume | 9 |
Issue | 3 |
Pages | 1068-1080 |
DOI | https://doi.org/10.1039/d1mh01383a |
Public URL | https://durham-repository.worktribe.com/output/1214927 |
Files
Published Journal Article
(5.1 Mb)
PDF
Publisher Licence URL
http://creativecommons.org/licenses/by/3.0/
Copyright Statement
This work is licensed under a Creative Commons Attribution 3.0 Unported License.
You might also like
Azaborine as a Versatile Weak Donor for Thermally Activated Delayed Fluorescence
(2023)
Journal Article
Downloadable Citations
About Durham Research Online (DRO)
Administrator e-mail: dro.admin@durham.ac.uk
This application uses the following open-source libraries:
SheetJS Community Edition
Apache License Version 2.0 (http://www.apache.org/licenses/)
PDF.js
Apache License Version 2.0 (http://www.apache.org/licenses/)
Font Awesome
SIL OFL 1.1 (http://scripts.sil.org/OFL)
MIT License (http://opensource.org/licenses/mit-license.html)
CC BY 3.0 ( http://creativecommons.org/licenses/by/3.0/)
Powered by Worktribe © 2024
Advanced Search