钝化
油胺
量子点
钙钛矿(结构)
材料科学
量子产额
涂层
光致发光
配体(生物化学)
化学工程
发光
三乙氧基硅烷
表面改性
纳米技术
光化学
光电子学
纳米颗粒
化学
图层(电子)
荧光
复合材料
物理
工程类
受体
量子力学
生物化学
作者
Xiaoling Guo,Huidong Xie,Wentao Cai,Fu Wang,Bing Xu,Chang Yang
标识
DOI:10.1021/acs.jpcc.3c05055
摘要
Inorganic metal halide CsPbX 3 (X = Cl, Br, and I) perovskite quantum dots (QDs) are widely used in light-emitting diodes, photodetectors, and solar cells due to their excellent optoelectronic properties. Their disadvantage is poor environmental stability, which can be improved to some extent by dynamic bonding of conventional organic acid/amine ligands to the surface of QDs. Here, we adopt an internal and external synergistic strategy by first introducing 4-sulfamoylbenzoic acid (4-SABA) during the synthesis process, which effectively modifies the uncoordinated Pb 2+ and Br – vacancies on the surface of QDs. Second, a layered SiO 2 substrate was generated by (3-aminopropyl) triethoxysilane hydrolysis to encapsulate the QDs, which finally achieved the dual protection effect of surface passivation and inorganic coating of the QDs. Results showed that the as-prepared 4-SABA-CsPbBr 3 /SiO 2 composites had a higher photoluminescence quantum yield (96%) and far more stability to water and ethanol than the oleic acid-/oleylamine-passivated QDs. This paper provides an effective way to prepare QD solutions with not only low cost but also high efficiency.
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