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9,9-Diphenyl- thioxanthene derivatives as host materials for highly efficient blue phosphorescent organic light-emitting diodes

机译:9,9-二苯基-噻吨并蒽衍生物用作高效蓝色磷光有机发光二极管的主体材料

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摘要

A series of 9,9-diphenyl-9H-thioxanthene derivatives with different valence states of sulfur atoms are reported as host materials in blue phosphorescent organic light-emitting diodes. Their photophysical, electrochemical and thermal properties, as well as device performance were thoroughly investigated to study their structure-property relationships, including the different carbazolyl linkage positions and valence states of sulfur atoms. Extremely low turn-on voltages of around 2.6 V for blue electrophosphorescence, which are already corresponding to the value of the emitted photon energy (hv)/electron charge (e), were achieved by utilizing the developed materials as hosts of the blue phosphor dopant iridium(III)bis(4,6-(difluorophenyl)-pyridinato-N,C-2') picolinate (FIrpic). Notably, a maximal power efficiency of 69.7 lm W-1 and an external quantum efficiency of 29.0% were achieved for an optimal device based on m-DCz-S consisting of the bivalent sulfur atom and meta-combined carbazolyl.
机译:据报道,一系列具有不同价态硫原子的9,9-二苯基-9H-噻吨衍生物是蓝色磷光有机发光二极管的主体材料。对它们的光物理,电化学和热学性质以及器件性能进行了彻底研究,以研究它们的结构性质关系,包括不同的咔唑基键合位置和硫原子的价态。通过将开发的材料用作蓝色磷光体掺杂剂的主体,可以实现约2.6 V的极低开启电压(用于蓝色电磷光),该电压已经对应于发射的光子能量(hv)/电子电荷(e)的值。吡啶甲酸铱(III)双(4,6-(二氟苯基)-吡啶基-N,C-2')(FIrpic)。值得注意的是,基于由二价硫原子和间位结合的咔唑基组成的m-DCz-S的最佳器件的最大功率效率为69.7 lm W-1,外部量子效率为29.0%。

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