激子
材料科学
蒽
共发射极
系统间交叉
荧光
有机发光二极管
光化学
接受者
光电子学
量子效率
纳米技术
化学
光学
物理
原子物理学
单重态
激发态
量子力学
图层(电子)
凝聚态物理
作者
Yuwei Xu,Xiaoming Liang,Yiqian Liang,Xiaomin Guo,Muddasir Hanif,Jiadong Zhou,Xuehong Zhou,Cong Wang,Jingwen Yao,Ruiyang Zhao,Dehua Hu,Xianfeng Qiao,Dongge Ma,Yuguang Ma
标识
DOI:10.1021/acsami.9b10823
摘要
A novel, efficient, deep-blue fluorescent emitter mPAC, with a meta-connected donor–acceptor structure containing phenanthroimidazole (PPI) as the donor and phenylcarbazole-substituted anthracene (An-CzP) as the acceptor, was designed and synthesized. The meta-linkage provided a highly twisted molecular conformation, which efficiently interrupts the intramolecular π-conjugation, resulting in a deep-blue emission. The optimized nondoped device based on mPAC displayed a deep-blue emission with a narrow full width at half-maximum of 56 nm and Commission Internationale de L’Eclairage coordinates of (0.16, 0.09). The maximum external quantum efficiency (EQE max ) is 6.76%, corresponding to a high exciton utilization efficiency (EUE) of 59.3–88.9%. Experimental results and theoretical analysis indicated that the high EUE is mainly ascribed to the reverse intersystem crossing (RISC) from T 2 to S 1, a “hot exciton” path in which the large T 2 –T 1 energy gap (1.45 eV) and small T 2 –S 1 energy difference (0.18 eV, T 2 > S 1 ) hamper the internal crossing from T 2 to T 1 and facilitate the RISC process. For the hot exciton path, the T 2 state can be feasibly arranged to a high energy level, forming a thermal equilibrium with S 1, even slightly higher than the deep-blue S 1 to realize an exergonic RISC process, which is usually difficult for the thermally activated delayed fluorescence emitters.
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