双极扩散
电致发光
材料科学
钙钛矿(结构)
量子效率
二极管
光电子学
发光二极管
带隙
双功能
纳米技术
化学
物理
结晶学
等离子体
生物化学
量子力学
催化作用
图层(电子)
作者
Chenwei Liu,Yongjie Liu,Shuxin Wang,Jiwei Liang,Cheng Wang,Fang Yao,Weijun Ke,Qianqian Lin,Ti Wang,Chen Tao,Guojia Fang
标识
DOI:10.1002/adom.202200276
摘要
Abstract Quasi‐two‐dimensional (quasi‐2D) perovskite light‐emitting diodes (PeLEDs) are considered as one of the most potential candidates in electroluminescence territory owing to their unique quantum confinement effect and excellent thermal stability of the light. Nevertheless, heterogeneous energy domain distribution leads to severe non‐radiative recombination in the process of energy transfer, which enormously hinders the performance and application of PeLEDs. Herein, an ambipolar amino acid, 5‐aminovaleric acid (5AVA), is demonstrated to be able to coordinate lead and halides simultaneously with its carboxyl and amidogen groups. The coordinated ambipolar molecule not only reconstitutes energy domains of perovskites but also minimizes the interfacial defects of PeLEDs. Accordingly, the presence of 5AVA in perovskite precursors leads to dramatic suppression of the n = 1 and n = 2 phases and accelerates energy transfer from wide bandgap domains to narrow bandgap ones. As a result, maximum external quantum efficiency (EQE) of 19.3% (18.20% ± 1.10%) is achieved in quasi‐2D green PeLEDs with current efficiency of 61.7 cd A −1 .
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