Issue 3, 2022

Diindolocarbazole – achieving multiresonant thermally activated delayed fluorescence without the need for acceptor units

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.

Graphical abstract: Diindolocarbazole – achieving multiresonant thermally activated delayed fluorescence without the need for acceptor units

Supplementary files

Article information

Article type
Communication
Submitted
26 avq 2021
Accepted
16 dek 2021
First published
24 yan 2022
This article is Open Access
Creative Commons BY license

Mater. Horiz., 2022,9, 1068-1080

Diindolocarbazole – achieving multiresonant thermally activated delayed fluorescence without the need for acceptor units

D. Hall, K. Stavrou, E. Duda, A. Danos, S. Bagnich, S. Warriner, A. M. Z. Slawin, D. Beljonne, A. Köhler, A. Monkman, Y. Olivier and E. Zysman-Colman, Mater. Horiz., 2022, 9, 1068 DOI: 10.1039/D1MH01383A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements