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Updated: Mar 2, 2026

Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Sterically Shielded Electron Transporting Material with Nearly 100% Internal Quantum Efficiency and Long Lifetime for
Dongdong Zhang1, Pengcheng Wei1, Deqiang Zhang1
1Key Laboratory of Organic Optoelectronics and Molecular Engineering of Ministry of Education, Department of Chemistry, Tsinghua University , Beijing 100084, China.
Abstract:
A high triplet energy (T1) is usually taken as the prerequisite of the good exciton confinement of electron transporting materials (ETMs); however, there is usually a tradeoff with large mobility and stability. Here, we demonstrated that good exciton confinement can also be realized utilizing a low-T1 ETM with a sterically shielding low-T1 unit. Given the short-range interaction of the Dexter energy transfer, the large steric side groups of the low-T1 ETM can effectively hinder the T1 of the emitters from being quenched by increasing the intermolecular distance. Based on this concept, a maximum external quantum efficiency (EQEmax) as high as 21.3% was observed in the sky-blue thermally activated delayed fluorescence device using a low-T1 ETM, with the EQE remaining at 21.2% at 1000 cd/m2 and 17.8% at 5000 cd/m2. Further, an EQEmax as high as 25.5%, a low turn-on voltage of 2.3 V, as well as a long T90 of over 400 h at an initial luminance of 5000 cd/m2 were achieved for green phosphorescent devices. This work highlights a viable strategy for developing high-performance ETMs, paving their way toward practical applications.

