量子产额
材料科学
磺酸盐
配体(生物化学)
光致发光
量子点
溴化物
离子
胺气处理
钙钛矿(结构)
光化学
化学工程
纳米技术
荧光
结晶学
无机化学
光电子学
有机化学
化学
钠
物理
工程类
受体
量子力学
冶金
生物化学
作者
Dandan Yang,Xiaoming Li,Wenhan Zhou,Shengli Zhang,Cuifang Meng,Ye Wu,Yue Wang,Haibo Zeng
标识
DOI:10.1002/adma.201900767
摘要
Abstract The stability and optoelectronic device performance of perovskite quantum dots (Pe‐QDs) are severely limited by present ligand strategies since these ligands exhibit a highly dynamic binding state, resulting in serious complications in QD purification and storage. Here, a “Br‐equivalent” ligand strategy is developed in which the proposed strong ionic sulfonate heads, for example, benzenesulfonic acid, can firmly bind to the exposed Pb ions to form a steady binding state, and can also effectively eliminate the exciton trapping probability due to bromide vacancies. From these two aspects, the sulfonate heads play a similar role as natural Br ions in a perfect perovskite lattice. Using this approach, high photoluminescence quantum yield (PL QY) > 90% is facilely achieved without the need for amine‐related ligands. Furthermore, the prepared PL QYs are well maintained after eight purification cycles, more than five months of storage, and high‐flux photo‐irradiation. This is the first report of high and versatile stabilities of Pe‐QD, which should enable their improved application in lighting, displays, and biologic imaging.
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