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Updated: Dec 11, 2025

Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Theoretical Study on Thermally Activated Delayed Fluorescence Emitters in White Organic Light-Emitting Diodes:
Feiyan Li1, Muzhen Li1, Jianzhong Fan1
1Shandong Key Laboratory of Medical Physics and Image Processing & Shandong Provincial Engineering and Technical Center of Light Manipulations, School of Physics and Electronics, Shandong Normal University, Jinan 250358, China.
Abstract:
Employing dual-emission thermally activated delayed fluorescence (TADF) molecules to fabricate single emitters in highly efficient white organic light-emitting diodes (WOLEDs) is still a challenge. In this work, a systematic study on the luminescence mechanism of three TADF molecules with blue-orange dual emission is performed. It is found that the quasi-axial (ax) conformer is responsible for blue normal fluorescence (NF), while the quasi-equatorial (eq) conformer is responsible for orange TADF. In addition, the upconversion for the TADF molecules happens from the first triplet state (T1) and the second triplet state (T2) to the first singlet state (S1) in the quasi-equatorial conformers. In addition, the transition from T1 to S1 and T2 to S1 also happens in the process of conformation transformation. Besides, our study also indicates that the donor with an asymmetric bond length in the six-membered ring could favor the generation of dual conformations and dual emission. Some molecules with PTZ or PXZ as donors are predicted as potential emitters with white light emission. Our research would favor the design of TADF emitters with dual emission in WOLEDs.
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