有机发光二极管
激子
咔唑
光电子学
猝灭(荧光)
材料科学
电致发光
量子效率
光化学
光致发光
化学
荧光
光学
纳米技术
物理
凝聚态物理
图层(电子)
作者
Kaiyuan Zhang,Xingdong Wang,Yufei Chang,Yuliang Wu,Shumeng Wang,Lixiang Wang
出处
期刊:Angewandte Chemie
[Wiley]
日期:2023-09-30
卷期号:62 (47): e202313084-e202313084
被引量:69
标识
DOI:10.1002/anie.202313084
摘要
Abstract The hyperfluorescence has drawn great attention in achieving efficient narrowband emitting devices based on multiple resonance thermally activated delayed fluorescence (MR‐TADF) emitters. However, achieving efficient solution‐processed pure blue hyperfluorescence devices is still a challenge, due to the unbalanced charge transport and serious exciton quenching caused by that the holes are easily trapped on the high‐lying HOMO (the highest occupied molecular orbital) level of traditional diphenylamine‐decorated emitters. Here, we developed two narrowband blue organoboron emitters with low‐lying HOMO levels by decorating the MR‐TADF core with weakly electron‐donating carbazoles, which could suppress the hole trapping effect by reducing the hole traps between host and MR‐TADF emitter from deep (0.40 eV) to shallow (0.14/0.20 eV) ones for facilitating hole transport and exciton formation, as well as avoiding exciton quenching. And the large dihedral angle between the carbazole and MR‐TADF core makes the carbazole act as a steric hindrance to inhibit molecular aggregation. Accordingly, the optimized solution‐processed pure blue hyperfluorescence devices simultaneously realize record external quantum efficiency of 29.2 %, narrowband emission with a full‐width at half‐maximum of 16.6 nm, and pure blue color with CIE coordinates of (0.139, 0.189), which is the best result for the solution‐processed organic light‐emitting diodes based on MR‐TADF emitters.
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