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Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Novel Robust Folded Thermally Activated Delayed Fluorescence Molecules for High-Performance OLEDs
Xia Lan1, Xiaoyang Guan1, Jiajie Zeng1
1State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Luminescence from Molecular Aggregates, South China University of Technology, Guangzhou, China.
Abstract:
Folded thermally activated delayed fluorescence (TADF) molecules based on through-space charge transfer (TSCT) have aroused increasing interest, but the electroluminescence (EL) efficiencies of most folded TADF molecules are still inferior, and their application as sensitizers for multi-resonance TADF (MR-TADF) emitters remains barely explored. Herein, two novel isomeric folded TADF molecules, f-TRZ-1 and f-TRZ-2, are constructed by using 2,4,6-triphenyl-1,3,5-triazine (TRZ) as acceptor, 9-phenylcarbazole (PC) as donor, and 11,12-dihydroindolo[2,3-a]carbazole (HIC) as bridge. They exhibit regular intramolecular packing structures with effective TSCT and enjoy ultrahigh thermal stability and balanced bipolar charge transport. Moreover, efficient organic light-emitting diodes (OLEDs) are fabricated using f-TRZ-1 and f-TRZ-2 as emitters, achieving maximum external quantum efficiencies (ηext,max) of up to 28.9%. f-TRZ-1 and f-TRZ-2 can perform as efficient sensitizers for the green MR-TADF emitter tCzphB-Fl, and the prepared hyperfluorescence OLEDs exhibit outstanding EL performances, with improved ηext,maxs of up to 37.8% and reduced efficiency roll-offs. This work demonstrates the promising potential of these folded TADF molecules as emitters and sensitizers for the fabrication of high-performance OLEDs.

