TADF polymer enables over 20% EQE in solution‐processed green fluorescent OLEDs

SmartMat Pub Date : 2024-02-15 DOI:10.1002/smm2.1272
L. Yan, Ning Su, Ying Yang, Xue Li, Jieting Sun, Shumeng Wang, Lei Zhao, Liming Ding, Junqiao Ding
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Abstract

Solution‐processed fluorescent organic light‐emitting diodes (OLEDs) are believed to be favorable for low‐cost, large‐area, and flexible displays but still suffer from the limited external quantum efficiency (EQE) below 5%. Herein, we demonstrate the EQE breakthrough by introducing a donor–acceptor type thermally activated delayed fluorescence (TADF) polymer as the sensitizer for the typical green‐emitting fluorescent dopants. Benefitting from their matched energy alignment, the unwanted trap‐assisted recombination directly on fluorescent dopant is prevented to avoid the additional loss of triplet excitons. Indeed, triplet excitons are mainly formed on the polymeric TADF sensitizer via a Langevin recombination and then spin‐flipped to singlet excitons due to the good upconversion capability. Followed by an efficient Förster energy transfer, both singlet and triplet excitons can be harvested by fluorescent dopants, leading to a promising solution‐processed green hyperfluorescence with a record‐high EQE of 21.2% (72.2 cd/A, 59.7 lm/W) and Commission Internationale de L'Eclairage coordinates of (0.32, 0.59). The results clearly highlight the great potential of solution‐processed fluorescent OLEDs based on TADF polymers as the sensitizer.
TADF 聚合物使溶液加工的绿色荧光 OLED 的 EQE 超过 20
溶液处理荧光有机发光二极管(OLED)被认为有利于实现低成本、大面积和柔性显示,但仍存在外部量子效率(EQE)低于 5%的问题。在此,我们通过引入一种供体-受体型热激活延迟荧光(TADF)聚合物作为典型绿色发光荧光掺杂剂的敏化剂,证明了 EQE 的突破。得益于它们匹配的能量排列,可以防止荧光掺杂剂直接发生不必要的陷阱辅助重组,从而避免三重激子的额外损失。事实上,三重激子主要是通过朗格文重组在聚合物 TADF 感光剂上形成的,然后由于良好的上转换能力而自旋翻转为单重激子。通过高效的佛斯特能量转移,单重激子和三重激子都能被荧光掺杂剂所捕获,从而产生前景广阔的溶液处理绿色超荧光,其 EQE 达到创纪录的 21.2%(72.2 cd/A,59.7 lm/W),国际照明委员会坐标为(0.32,0.59)。这些结果清楚地凸显了以 TADF 聚合物为敏化剂的溶液处理荧光 OLED 的巨大潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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