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Updated: Jun 3, 2025

Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
AIE-Active Circularly Polarized Thermally Activated Delayed Fluorescence Emitters for Stable Solution-Processed
Yuxia Zhang1, Fan Lu Kong1, Hao Yu Chen1
1State Key Laboratory for Organic Electronics and Information Displays and Jiangsu Key Laboratory for Biosensors, Institute of Advanced Mate-rials (IAM), Nanjing University of Posts and Telecommunications, Nanjing, 210023, China.
Abstract:
Circularly polarized organic light-emitting diodes (CP-OLEDs) have significant promise for naked-eye 3D displays. However, most devices are fabricated using vacuum deposition technology, and development of efficient solution-processed CP-OLEDs, particularly those exhibiting low efficiency roll-off, remains a formidable challenge. This research successfully designed and synthesized two pairs of thermally activated delayed fluorescence (TADF) enantiomers through isomer engineering, namely (R/S)-N-5-TPA and (R/S)-N-4-TPA, which features fifth and fourth substitution sites of phthalimide (acceptor) by tri-phenylamine (donor), respectively. Both molecules displayed aggregation-induced emission (AIE) properties. Notably, the CP-OLED devices, fabricated by solution-process, exhibited vivid blue-green and green emission with the maximum current efficiency of 7.4 and 29.6 cd A-1, the external quantum efficiency of 2.7 % and 10.2 %, and the low efficiency roll-off of 3.7 % and 16.7 %. Moreover, these devices demonstrated CP-EL signals with gEL values of +6.61×10-4 /-6.84×10-4 and +1.13×10-3/-1.25×10-3, respectively.
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