有机发光二极管
激子
兴奋剂
材料科学
光电子学
电致发光
量子效率
猝灭(荧光)
发光
消灭
单重态
荧光
纳米技术
光学
激发态
物理
原子物理学
凝聚态物理
量子力学
图层(电子)
作者
Huijun Liu,Jiajie Zeng,Jingjing Guo,Han Nie,Zujin Zhao,Ben Zhong Tang
标识
DOI:10.1002/anie.201802060
摘要
Abstract Non‐doped organic light‐emitting diodes (OLEDs) possess merits of higher stability and easier fabrication than doped devices. However, luminescent materials with high exciton use are generally unsuitable for non‐doped OLEDs because of severe emission quenching and exciton annihilation in neat films. Herein, we wish to report a novel molecular design of integrating aggregation‐induced delayed fluorescence (AIDF) moiety within host materials to explore efficient luminogens for non‐doped OLEDs. By grafting 4‐(phenoxazin‐10‐yl)benzoyl to common host materials, we develop a series of new luminescent materials with prominent AIDF property. Their neat films fluoresce strongly and can fully harvest both singlet and triplet excitons with suppressed exciton annihilation. Non‐doped OLEDs of these AIDF luminogens exhibit excellent luminance (ca. 100000 cd m −2 ), outstanding external quantum efficiencies (21.4–22.6 %), negligible efficiency roll‐off and improved operational stability. To the best of our knowledge, these are the most efficient non‐doped OLEDs reported so far. This convenient and versatile molecular design is of high significance for the advance of non‐doped OLEDs.
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