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Achievement of High-Performance Nondoped Blue OLEDs Based on AIEgens via Construction of Effective High-Lying Charge-Transfer State

机译:基于Aiegens的高性能Nondoped蓝olds实现有效高位电荷转移状态的实现

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Abstract There remains an urgent demand for high‐quality blue luminogens that can simultaneously achieve high photoluminescence quantum yield (PLQY) in film and high exciton utilization efficiency (EUE) in the electroluminescence (EL) process. In this study, a referable molecular design strategy is developed for blue luminogens via constructing low‐lying locally excited (LE) state with an aggregation‐induced emission (AIE) characteristic and high‐lying charge‐transfer (CT) state for the effective triplet‐to‐singlet conversion channel. 2TriPE‐BPI‐MCN with the insertion of p‐cyano and o‐methyl groups is designed to compare with its matrix framework (2TriPE‐BPI). They have analogous properties of the lowest singlet (S1) states with blue emission and free of concentration quenching in film; however, 2TriPE‐BPI‐MCN exhibits unusual response for hydrostatic pressure owing to its S2 state CT characteristics. Therefore, 2TriPE‐BPI‐MCN can harness more electrogenerated excitons than 2TriPE‐BPI, resulting in a better EL performance in nondoped blue organic light‐emitting diodes (OLEDs) (CIEx,y = 0.153, 0.147) with high external quantum efficiency of 4.6% and negligible efficiency roll‐off. These findings could open a feasible avenue to develop high‐quality blue luminogens for high‐performance nondoped blue OLEDs.
机译:摘要仍然存在对高质量的蓝色发光剂的迫切需求,其可以在电致发光(EL)过程中同时实现薄膜和高激子利用效率(EUE)的高光致发光量子产量(PLQY)。在这项研究中,通过构造具有聚集诱导的发射(AIE)特征和高位电荷转移(CT)状态的低洼局部激发(LE)状态,为蓝色发光型和高位电荷转移(CT)状态而开发了可转型分子设计策略。 -to-singlet转换信道。 2Tripe-BPI-MCN插入p-氰基和O-甲基的设计用于与其基质框架(2TRIPE-BPI)进行比较。它们具有具有蓝色排放的最低单线(S1)状态的类似性质,并且在薄膜中没有浓度猝灭;然而,由于其S2状态CT特性,2TRIPH-BPI-MCN对静压压力表现出不寻常的响应。因此,2TRIPH-BPI-MCN可以利用比2TRIPH-BPI更高的电流激子,导致具有高外部量子效率的NONDOPED蓝色有机发光二极管(CIEX,Y = 0.153,0.147)中更好的EL性能。4.6效率下降%,效率可忽略不计。这些调查结果可以开辟一个可行的途径,以开发高品质的蓝色发光剂,适用于高性能的蓝色OLED。

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