Lv Xialei, Miao Jingsheng, Liu Meihui, Peng Qian, Zhong Cheng, Hu Yuxuan, Cao Xiaosong, Wu Han, Yang Yiyu, Zhou Changjiang, Ma Jiazhi, Zou Yang, Yang Chuluo
Shenzhen Key Laboratory of New Information Display and Storage Materials, College of Materials Science and Engineering, Shenzhen University, Shenzhen, 518060, P. R. China.
School of Chemical Sciences, University of Chinese Academy of Sciences, Beijing, 100049, P. R. China.
Angew Chem Int Ed Engl. 2022 Jul 18;61(29):e202201588. doi: 10.1002/anie.202201588. Epub 2022 May 31.
Multi-resonance TADF (MR-TADF) emitters are promising for high-resolution OLEDs, but the concurrent optimization of excited-state dynamics and color purity remains a tough challenge. Herein, three deep-blue MR-TADF compounds (BN1-BN3) featuring gradually enlarged ring-fused structures and increased rigidity are accessed by lithium-free borylation in high yields from the same precursor, with all the emitters possessing CIE coordinates below 0.08. Structure-property investigations demonstrate a strategic improvement of the oscillator strength (f ) and acceleration of the reverse intersystem crossing (RISC) process by extending the π-skeleton, where BN3 realizes a maximum external quantum efficiency (EQE) of 37.6 % and reduced roll-off, thus showing the best efficiency reported for deep-blue TADF OLEDs. The internal regulation of the efficiency and color purity of these compounds validate the general effectiveness to achieve advanced deep-blue narrowband emitters with higher-order boron/nitrogen-based MR motifs.
多共振热活化延迟荧光(MR-TADF)发光体对于高分辨率有机发光二极管(OLED)很有前景,但激发态动力学和色纯度的同时优化仍然是一项艰巨的挑战。在此,通过无锂硼化反应,以高产率从同一前体获得了三种具有逐渐增大的稠环结构和增加刚性的深蓝色MR-TADF化合物(BN1-BN3),所有发光体的CIE坐标均低于0.08。结构-性能研究表明,通过扩展π骨架可战略性地提高振子强度(f)并加速反向系间窜越(RISC)过程,其中BN3实现了37.6%的最大外量子效率(EQE)并降低了效率滚降,从而展现出深蓝色TADF OLED所报道的最佳效率。这些化合物的效率和色纯度的内部调控验证了实现具有高阶硼/氮基MR motif的先进深蓝色窄带发光体的总体有效性。