Boron-Based Multi-Resonance TADF Emitter with Suppressed Intermolecular Interaction and Isomer Formation for Efficient Pure Blue OLEDs

被引:74
作者
Cheon, Hyung Jin [1 ,2 ]
Shin, Youn-Seob [3 ]
Park, Noh-Hwal [4 ]
Lee, Jeong-Hwan [3 ,4 ]
Kim, Yun-Hi [1 ,2 ]
机构
[1] Gyeongsang Natl Univ, Dept Chem, Jinju 52828, South Korea
[2] Gyeongsang Natl Univ, RIGET, Jinju 52828, South Korea
[3] Inha Univ, Dept Mat Sci & Engn, Incheon 22212, South Korea
[4] Inha Univ, 3D Convergence Ctr, Incheon 22212, South Korea
基金
新加坡国家研究基金会;
关键词
blue organic light-emitting diode (OLED); DABNA; multi-resonance emitters; thermally activated delayed fluorescent (TADF) emitters; ACTIVATED DELAYED FLUORESCENCE; DIODES; MOLECULES;
D O I
10.1002/smll.202107574
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Multi-resonance (MR) thermally activated delayed fluorescent (TADF) emitters are highly attractive due to their superior color purity as well as efficient light-harvesting ability from singlets and triplets. However, boron and nitrogen-based MR-TADF emitters suffer from their strong pi-pi interaction owing to their rigid flat cores. Herein, a boron-based multi-resonance blue TADF emitter with suppressed intermolecular interaction and isomer formation is developed through a simple synthetic process by introducing meta-xylene and meta-phenyphenyl groups to the core. The MR-TADF emitter, mBP-DABNA-Me, shows a narrowband blue emission with a peak at 467 nm, along with full width at half maximum of 28 nm, and photoluminescence quantum yield of 97%. Notably, highly efficient pure blue organic light-emitting diode (OLED) is realized using mBP-DABNA-Me, showing a maximum external quantum efficiency of 24.3% and a stable blue emission with a Commission Internationale de L'Eclairage coordinate of (0.124, 0.140). The color purity of the OLED is maintained at a high doping concentration of over 20%, attributed to the suppressed intermolecular interaction between the MR emitters.
引用
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页数:7
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