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Updated: Feb 28, 2026

Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Efficient Sky-Blue Narrow-Band Thermally Activated Delayed Fluorescence Emitters Integrating Charge-Transfer and
Xinyu Li1, Huixia Xu1, Zixuan Wei1
1Key Laboratory of Interface Science and Engineering in Advanced Materials, Ministry of Education, Taiyuan University of Technology, Taiyuan 030024, P. R. China.
Abstract:
Organic emitters with narrow-band emission are of great significance for realizing high-definition organic light-emitting diodes (OLEDs). The multiple-resonance thermally activated delayed fluorescence (MR-TADF) is constrained by slow reverse intersystem crossing (RISC). Herein, we proposed a strategy to adjust their excited state natures by linking MR units with an indolocarbazole (ICz) donor. The designed emitters, namely, ICz-BN and tICZ-BN, showed the advantages of MR-TADF with a narrow full-width at half-maximum (FWHM) along with a minimal triplet-singlet energy gap (ΔEST). The fast radiative decay (>107 s-1) and large RISC rate constants (kRISC > 105 s-1) were realized. The maximum external quantum efficiency (EQEmax) of 28.5% and 24.7% were achieved along with the FWHM of 36 and 34 nm and emission peaks of 491 and 489 nm. The tICz-BN-based device exhibited good resistance to concentration quenching. This strategy provides a feasible approach for designing high-efficiency narrow-band sky-blue TADF emitters.
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