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Updated: Oct 22, 2025

Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Realizing Record-High Electroluminescence Efficiency of 31.5 % for Red Thermally Activated Delayed Fluorescence
Zheyi Cai1, Xing Wu1, Hao Liu1
1State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Luminescence from Molecular Aggregates, South China University of Technology, Guangzhou, 510640, China.
Abstract:
Tailor-made red thermally activated delayed fluorescence (TADF) molecules comprised of an electron-withdrawing pyrazino[2,3-f][1,10]phenanthroline-2,3-dicarbonitrile core and various electron-donating triarylamines are developed. They can form intramolecular hydrogen-bonding, which is conducive to improving emission efficiency and promoting horizontal orientation and show near infrared (NIR) emissions (692-710 nm) in neat films and red delayed fluorescence (606-630 nm) with high photoluminescence quantum yields (73-90%) in doped films. They prefer horizontal orientation with large horizontal dipole ratios in films, rendering high optical out-coupling factors (0.39-0.41). Their non-doped OLEDs exhibit NIR lights (716-748 nm) with maximum external quantum efficiencies (ηext,max ) of 1.0-1.9%. And their doped OLEDs radiate red lights (606-648 nm) and achieve record-beating ηext,max of up to 31.5%. These new red TADF materials should have great potentials in display and lighting devices.
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