期刊
JOURNAL OF MATERIALS CHEMISTRY C
卷 9, 期 26, 页码 8233-8238出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1tc01741a
关键词
-
资金
- Institute for Basic Science [IBS-R10-A1]
- [NRF-2020R1A2C2100872]
Organic phosphorescent emitters incorporating alkyl substituents into the N-phenylphenoselenazine core have been developed, showing efficient phosphorescence in amorphous film and pure phosphorescence in electroluminescence devices, with the sterically hindered alkyl substituents playing a key role in triplet-exciton-quenching and achieving high external quantum efficiency up to 9.0%.
Purely organic phosphorescent emitters have been developed with the incorporation of alkyl substituents into the N-phenylphenoselenazine core. The new emitter displayed efficient phosphorescence in amorphous film and featured pure phosphorescence in electroluminescence devices due to strong spin-orbit coupling for triplet to singlet transition. The steric bulk of the alkyl substituent, which could hamper triplet-exciton-quenching, is found to be essential for high efficiency of the device, and the tert-butyl group induces the highest external quantum efficiency (EQE) of 9.0%.
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