Selenium-integrated multi-resonant thermally activated delayed fluorescent emitters showing improved reverse intersystem crossing rate and chirality

27 March 2025, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Nitrogen/carbonyl (N/C=O) based multi-resonant thermally activated delayed fluorescence (MR-TADF) emitters are attractive due to their bright, narrowband emission and the ease with which they can be synthesized. However, the photophysics of most of the examples of this class of emitters suffer from slow reverse intersystem crossing (RISC) because of their relatively large singlet-triplet energy gap (EST). Thus, the organic light-emitting diodes (OLEDs) with emitters from this class typically show severe efficiency roll-off. Here, two MR-TADF emitters DiKTaSe and tBuCz-DiKTaSe have been designed and synthesized. The introduction of selenium in the form of an annelated benzoselenophene enhances spin-orbit coupling and increases the RISC rate. The presence of a twisted ortho-substituted tert-butylcarbazole moiety in tBuCz-DiKTaSe helps to increase the intermolecular distance between adjacent emitters and suppresses aggregation-caused quenching of the emission in films. In addition, the large size of the selenium atom and long C-Se bonds induce helical chirality in both DiKTaSe and tBuCz-DiKTaSe. Finally, the OLEDs with DiKTaSe showed maximum external quantum efficiency (EQEmax) of 22.7% while OLEDs with tBuCz-DiKTaSe showed a higher EQEmax of 27.8% and less-pronounced efficiency roll-off, with EQE100/EQE1000 of 23.5/12.5%. These efficiency values are amongst the highest of devices employing DiKTa-based emitters. Our work provides key insight into how to judiciously employ heavy atoms to increase the performance of the emitter and the device.

Keywords

multi-resonant thermally activated delayed fluorescence
heavy atom effect
aggregation-caused quenching
helicene
organic light-emitting diode

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