有机发光二极管
量子效率
材料科学
轨道能级差
共发射极
紫外线
荧光
光电子学
光化学
接受者
激发态
二极管
分子内力
纳米技术
光学
化学
分子
原子物理学
有机化学
物理
图层(电子)
凝聚态物理
作者
Yanju Luo,Shuaibing Li,Yihuan Zhao,Chuan Li,Zhenguo Pang,Yan Huang,Minghui Yang,Liang Zhou,Xujun Zheng,Xuemei Pu,Zhiyun Lu
标识
DOI:10.1002/adma.202001248
摘要
Abstract Owing to the difficulty in acquiring compounds with combined high energy bandgaps and lower‐lying intramolecular charge‐transfer excited states, the development of ultraviolet (UV) thermally activated delayed fluorescence (TADF) materials is quite challenging. Herein, through interlocking of the diphenylsulfone (PS) acceptor unit of a reported deep‐blue TADF emitter (CZ‐PS) by a dimethylmethylene bridge, CZ‐MPS, a UV‐emissive TADF compound bearing a shallower LUMO energy level and a more rigid structure than those of CZ‐PS is achieved. This represents the first example of a UV‐emissive TADF compound. Organic light‐emitting diode (OLED) using CZ‐MPS as the guest material can emit efficient UV light with emission maximum of 389 nm and maximum total external quantum efficiency (EQE max ) of 9.3%. Note that this EQE max value is twice as high as the current record EQE max (4.6%) for UV‐OLEDs. This finding may shed light on the molecular design strategy for high‐performance UV‐OLED materials.
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