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Updated: Jan 4, 2026

Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Bridging Small Molecules to Conjugated Polymers: Efficient Thermally Activated Delayed Fluorescence with a
Jiancheng Rao1,2, Xinrui Liu1,3, Xuefei Li1,3
1State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, 130022, P. R. China.
Abstract:
Based on a "TADF + Linker" strategy (TADF=thermally activated delayed fluorescence), demonstrated here is the successful construction of conjugated polymers that allow highly efficient delayed fluorescence. Small molecular TADF blocks are linked together using a methyl-substituted phenylene linker to form polymers. With the growing number of methyl groups on the phenylene, the energy level of the local excited triplet state (3 LEb ) from the delocalized polymer backbone gradually increases, and finally surpasses the charge-transfer triplet state (3 CT). As a result, the diminished delayed fluorescence can be recovered for the tetramethyl phenylene containing polymer, revealing a record-high external quantum efficiency (EQE) of 23.5 % (68.8 cd A-1 , 60.0 lm W-1 ) and Commission Internationale de l'Eclairage (CIE) coordinates of (0.25, 0.52). Combined with an orange-red TADF emitter, a bright white electroluminescence is also obtained with a peak EQE of 20.9 % (61.1 cd A-1 , 56.4 lm W-1 ) and CIE coordinates of (0.36, 0.51).
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