Issue 22, 2022

Highly efficient thermally activated delayed fluorescence emitter based on the 5H-benzo[d]benzo[4,5]imidazo[1,2-a]imidazole donor

Abstract

In this study, a donor–π-acceptor-type thermally activated delayed fluorescence (TADF) emitter (BzITz) was designed and synthesized using 5H-benzo[d]benzo[4,5]imidazo[1,2-a]imidazole as a fused rigid electron donor, and a benzonitrile merged triazine unit as an electron acceptor. The effects of the fused rigid donor unit on the photophysical and electroluminescence properties of the TADF emitter were thoroughly explored. Compared with a reported emitter based on carbazole in a previous study, photophysical analysis results showed that BzITz exhibited a relatively small singlet–triplet energy splitting, a short delayed fluorescence lifetime, and a high photoluminescence quantum yield. Consequently, an organic light-emitting diode fabricated using the BzITz emitter exhibited an improved device performance with an external quantum efficiency of 24.0%, a current efficiency of 49.4 cd A−1, and a low-efficiency roll-off. These findings show that the use of fused rigid donors can play a critical role in the design of efficient TADF emitters.

Graphical abstract: Highly efficient thermally activated delayed fluorescence emitter based on the 5H-benzo[d]benzo[4,5]imidazo[1,2-a]imidazole donor

Supplementary files

Article information

Article type
Research Article
Submitted
10 ⵖⵓⵛ 2022
Accepted
19 ⵛⵓⵜ 2022
First published
21 ⵛⵓⵜ 2022

Mater. Chem. Front., 2022,6, 3382-3390

Highly efficient thermally activated delayed fluorescence emitter based on the 5H-benzo[d]benzo[4,5]imidazo[1,2-a]imidazole donor

M. M. Raikwar, S. C. Kim and J. Y. Lee, Mater. Chem. Front., 2022, 6, 3382 DOI: 10.1039/D2QM00806H

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