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Updated: May 20, 2025

Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Through-Space Interactions Enable Aggregation-Induced Quenching Suppression and Spin-Flipping Enhancement of
Shangru Li1,2, Jia-Ming Jin1,2, Jia-Xiong Chen1,2
1School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou 510006, P. R. China.
Abstract:
Multiple resonance (MR) thermally activated delayed fluorescence (TADF) materials hold significant potential for applications in high color purity and highly efficient organic light-emitting diodes (OLEDs). However, their inherently large planar structures often result in severe aggregation-induced quenching and slow spin-flip processes, presenting significant challenges that limit their practical applications. In this study, we designed and synthesized two MR-TADF molecules, tCON-Cz and tCON-2tBuCz, by incorporating a tCON backbone with carbazole or 3,6-di-tert-butylcarbazole at the ortho position of the phenyl ring. This strategic design introduces a highly twisted three-dimensional structure, effectively mitigating aggregation-induced quenching. Additionally, it creates a through-space charge transfer channel that facilitates reverse intersystem crossing, thereby enhancing TADF efficiency. As a result, both molecules exhibit high photoluminescence quantum yields. When incorporated into devices, these OLEDs demonstrated remarkable performance, achieving high external quantum efficiencies of 23.70% for tCON-Cz and 22.84% for tCON-2tBuCz at doping concentrations as high as 20%. Notably, both devices retained the narrow full width at half-maximum of around 36 nm, consistent with the parent tCON skeleton, ensuring superior color purity.
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