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
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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