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Low efficiency roll-off phosphorescent organic light-emitting devices using thermally activated delayed fluorescence hosts materials based 1, 2, 4-triazole acceptor

机译:使用热激活的延迟荧光的低效率滚降磷光有机发光器件以基于1,2,4-三唑受体的材料为主体

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摘要

The host in phosphrescent organic light emitting devices (PhOLEDs), showing the thermally activated delayed fluorescence (TADF) charateristic, can effectively overcome the efficiency roll-off. Herein, six bipolar compounds with donor-pi-acceptor (D-pi-A) and D-pi-A-pi-D structures have been synthesized using 1,2,4-triazole derivative (TAZ) as an acceptor and phenothiazine (PTZ), phenoxazine (PXZ), and 9, 9-dimethylacridane (DMAC) as donors. The molecular structures were confirmed by H-1 NMR, C-13 NMR and X-ray single-crystal diffractions. The large steric hindrance endows these molecules with typical TADF features, including the small singlet-triplet energy splitting (Delta E-ST) of 0.08-0.30 eV and completely spatially separate highest occupied molecular orbitals (HOMO) and the lowest unoccupied molecular orbitals (LUMO) electron densities. The PhOLEDs hosted by these novel TADF materials display excellent performances with low efficiency roll-off.
机译:磷光有机发光器件(PhOLED)中的主机具有热激活延迟荧光(TADF)特征,可以有效克服效率下降的问题。在此,使用1,2,4-三唑衍生物(TAZ)作为受体和吩噻嗪(D-pi-A)和D-pi-A-pi-D结构合成了六种双极性化合物。 PTZ),吩恶嗪(PXZ)和9、9-二甲基ac啶(DMAC)作为供体。通过H-1 NMR,C-13 NMR和X射线单晶衍射确认了分子结构。大的位阻使这些分子具有典型的TADF特征,包括0.08-0.30 eV的小单重态-三重态能量分裂(Delta E-ST)以及在空间上完全分开的最高占据分子轨道(HOMO)和最低未占据分子轨道(LUMO) )电子密度。这些新颖的TADF材料承载的PhOLED具有出色的性能和低效率的滚降。

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