系统间交叉
有机发光二极管
激子
苯甲腈
荧光
蒽
光化学
光电子学
磷光有机发光二极管
化学
光致发光
深蓝色
激发态
材料科学
单重态
光学
物理
纳米技术
原子物理学
有机化学
图层(电子)
量子力学
作者
Minting Ouyang,Runda Guo,He Jiang,Lei Wang,Wai‐Yeung Wong
标识
DOI:10.1016/j.jlumin.2023.120069
摘要
Two new emitters based on anthracene core, 6-(10-phenylanthracen-9-yl)nicotinonitrile (CNPyAnPh) and 4-(10-(pyridin-2-yl)anthracen-9-yl)benzonitrile (CNPhAnPy) are designed and synthesized for realizing blue and deep blue organic light-emitting diodes (OLEDs). Both CNPyAnPh and CNPhAnPy show nearly orthogonal structures and the suppressed π-conjugation is favorable for blue and even deep blue emission. According to the theoretical calculations, small energy differences between T2 and S1 are observed in these two isomers, endowing the “hot exciton” channel. Furthermore, the S1 of CNPyAnPh possesses both locally excited (LE) and charge transfer (CT) components. By employing CNPyAnPh and CNPhAnPy as the emissive guests in the devices, their maximum external quantum efficiencies (EQEmaxs) are 4.15% and 3.71%, respectively. Thanks to the “hot exciton” and hybrid local and charge transfer (HLCT) properties, the exciton utilization efficiencies (EUEs) of two molecules are higher than 25%, 42% for CNPyAnPh and 34% for CNPhAnPy. The Commission International de l’Eclairage (CIE) coordinate of CNPhAnPy is (0.15, 0.08), approaching the National Television System Committee (NTSC) standard index for pure blue emission.
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