有机发光二极管
量子效率
材料科学
磷光
兴奋剂
光电子学
系统间交叉
荧光
亮度
光化学
光学
纳米技术
单重态
化学
物理
图层(电子)
核物理学
激发态
作者
Chunya Du,Hui Liu,Zhuang Cheng,Shao‐Qin Zhang,Zhi‐Rong Qu,Dezhi Yang,Xianfeng Qiao,Zujin Zhao,Ping Lü
标识
DOI:10.1002/adfm.202304854
摘要
Abstract The pursuit for efficient deep blue material is an ever‐increasing issue in organic optoelectronics field. It is a long‐standing challenge to achieve high external quantum efficiency (EQE) exceed 10% at brightness of 1000 cd m −2 with a Commission International de L'Eclairage (CIE y ) <0.08 in non‐doped organic light‐emitting diodes (OLEDs). Herein, this study reports a deep blue luminogen, PPITPh, by bonding phenanthro[9,10‐d]imidazole moiety with m‐terphenyl group via benzene bridge. The non‐doped OLED based on PPITPh exhibits an exceptionally high EQE of 11.83% with a CIE coordinate of (0.15, 0.07). The EQE still maintains 10.17% at the brightness of 1000 cd m −2 , and even at a brightness as high as 10000 cd m −2 , an EQE of 7.5% is still remained, representing the record‐high result among non‐doped deep‐blue OLEDs at 1000 cd m −2 . The unprecedented device performance is attributed to the reversed intersystem crossing process through hot exciton mechanism. Besides, the maximum EQE of orange phosphorescent OLED with PPITPh as host is 32.02%, and remains 31.17% at the brightness of 1000 cd m −2 . Such minimal efficiency roll‐off demonstrates that PPITPh is also an excellent phosphorescent host material. The result offers a new design strategy for the enrichment of high‐efficiency deep blue luminogen.
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