钙钛矿(结构)
钝化
二极管
材料科学
发光二极管
光电子学
相(物质)
氧化物
激子
结晶
量子效率
化学物理
氢
氢键
图层(电子)
化学工程
纳米晶
工作(物理)
反应性(心理学)
纳米技术
带隙
蒸发
阳极
量子点
相变
结晶学
作者
Zixi Shen,Hong-Yi Xie,Jinghui Li,Shuwen Yan,Jianfeng Ou,Guoji Zheng,Luying Li,Boxiang Song,Jiajun Luo,Jiang Tang
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2025-09-16
卷期号:10 (10): 4941-4947
被引量:4
标识
DOI:10.1021/acsenergylett.5c02099
摘要
Thermally evaporated quasi-two-dimensional (quasi-2D) perovskite light-emitting diodes (PeLEDs) offer a route toward next-generation display technology. However, their performance has lagged behind solution-processed devices. Here, we introduce an in situ phase regulation strategy by co-evaporating a multifunctional ligand, tris(trifluoromethyl)phosphine oxide (TFPPO). The fluorine atoms in TFPPO form hydrogen bonds with the N–H groups of phenylethylammonium (PEA), suppressing the disordered incorporation of PEA and slowing the crystallization of low-n phases. This interaction promotes a more uniform phase distribution and enhances exciton funneling through energy gradients. Besides, the P═O groups of TFPPO could also passivate undercoordinated Pb2+ defects. As a result, we achieved a record external quantum efficiency (EQE) of 17.5% among thermally evaporated PeLEDs. Furthermore, the optimized emissive layer is seamlessly integrated into a 6.67 in. active-matrix TFT-driven display panel, demonstrating the practical viability of this approach for scalable perovskite display technologies.
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