期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 85, 期 16, 页码 10628-10637出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.joc.0c01200
关键词
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资金
- National Key R&D Program of China [2016YFB0400700]
- National Natural Science Foundation of China [51773141, 51873139, 61961160731]
- Natural Science Foundation of Jiangsu Province of China [BK20181442]
- Collaborative Innovation Center of Suzhou Nano Science Technology
- Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
- 111 Project of The State Administration of Foreign Experts Affairs of China
Intramolecular spatial charge transfer (ISCT) plays a critical role in determining the optical and charge transport properties of thermally activated delayed fluorescence (TADF) materials. Herein, a new donor/acceptor-type TADF compound based on rigid dibenzothiophene sulfone (DBTS) moiety, STF-DBTS, was designed and synthesized. Fluorene unit was used as a rigid linker to position the rigid acceptor and donor subunit in close vicinity with control over their spacing and molecular structure and to achieve high photoluminescence quantum yield (similar to 53%) and TADF property. For comparison purposes, we constructed the more flexible STF-DPS with a less rotationally constrained diphenylsulphone (DPS) acceptor instead of the rigid DBTS units, and STF-DPS showed no TADF properties and lower PLQY (16.0%). Organic light-emitting diodes (OLEDs) based on STF-DBTS achieve an external quantum efficiency (EQE) of 10.3% at 488 nm, which is a fivefold improvement in EQE with respect to STF-DPS.
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