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Bipolar host materials for high-efficiency blue phosphorescent and delayed-fluorescence OLEDs

机译:用于高效蓝色磷光和延迟荧光OLED的双极性主体材料

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A series of small molecular isomers, namely o-CzCN, m-CzCN, and p-CzCN, are developed for use as bipolar hosts in blue phosphorescent and fluorescent organic light-emitting diodes (OLEDs). Cyano (CN) substituted phenyl is selected as the n-type unit and N-phenyl-substituted carbazole as the p-type unit. By adjusting the ortho-, meta-, and para-linking styles of the functional units, the physical parameters are regularly tuned to a large extent. The study of complete spatial separation of frontier molecular orbitals and single-carrier devices confirm the bipolar feature. Blue phosphorescent and thermally activated delayed fluorescence (TADF) OLEDs were fabricated using iridium(III) bis(4,6-(difluorophenyl)pyridinato-N,C-2')picolinate (FIrpic) and 1,2-bis(carbazol-9-yl)-4,5-dicyanobenzene (2CzPN) as doped emitters. A maximum current efficiency of 46.81 cd A(-1) and an external quantum efficiency of 23.14% were achieved for the phosphorescent OLED with the m-CzCN host. Furthermore, high efficiencies of 29.23 cd A(-1) and 14.98% were obtained for the 2CzPN based blue TADF device with the o-CzCN host, which are higher than the best literature value of 13.6% for 2CzPN devices. Both m-CzCN and o-CzCN always perform better than p-CzCN. The influence of the chemical structures on their properties and performance is interpreted for these CN-decorated host materials.
机译:开发了一系列小分子异构体,即o-CzCN,m-CzCN和p-CzCN,用作蓝色磷光和荧光有机发光二极管(OLED)中的双极性主体。选择氰基(CN)取代的苯基作为n型单元,选择N-苯基取代的咔唑作为p型单元。通过调整功能单元的邻位,间位和对位链接样式,可以在很大范围内定期调整物理参数。对前沿分子轨道和单载体装置的完全空间分离的研究证实了双极特征。使用铱(III)双(4,6-(二氟苯基)吡啶并-N,C-2')吡啶甲酸(FIrpic)和1,2-双(咔唑-9)制备蓝色磷光和热活化延迟荧光(TADF)OLED。 -yl)-4,5-二氰基苯(2CzPN)作为掺杂的发射极。具有m-CzCN主体的磷光OLED的最大电流效率为46.81 cd A(-1),外部量子效率为23.14%。此外,对于带有o-CzCN主机的基于2CzPN的蓝色TADF器件,获得了29.23 cd A(-1)的高效率和14.98%的效率,高于2CzPN器件的最佳文献值13.6%。 m-CzCN和o-CzCN总是比p-CzCN表现更好。对于这些经过CN装饰的主体材料,可以解释化学结构对其性能和性能的影响。

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