硫系化合物
纳米晶
水溶液
化学
吸附
离子
纳米技术
壳体(结构)
卤化物
水分
化学工程
制作
光电子学
无机化学
材料科学
物理化学
复合材料
有机化学
替代医学
病理
工程类
医学
作者
Keqiang Chen,Dan Liŭ,Weiqi Lu,Kaihuai Zhuo,Guogang Li
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2024-01-17
卷期号:63 (4): 2247-2256
被引量:2
标识
DOI:10.1021/acs.inorgchem.3c04210
摘要
Shelling with chalcogenides on the surface of lead halide perovskite (LHP) nanocrystals (NCs) is believed to be an effective approach to increase their stability under high-moisture/aqueous conditions, which is important for LHP NC-based optoelectronic devices. However, it is still a challenge to prepare high-quality LHP/chalcogenide core/shell NCs with moisture/aqueous stability. In this work, a surface-defect-induced strategy is carried out to facilitate the adsorption of Br– ions and subsequently Zn2+ ions to preform a bipolar surface, which reduces the energy barrier at the CsPbBr3/ZnS interface and promotes the epitaxial growth of the ZnS shell layer. The aqueous stability of the as-received NCs shows an increase of over 12 times compared to that of the original one. Likewise, Mn2+ ions are introduced to further reduce the geometric symmetry mismatch and defect density at the CsPbBr3/ZnS interface. Interestingly, aqueous stability characterizations illustrate negligible degradation even after 230 min of ultrasonication, suggesting their outstanding stability. This work proposes an effective approach to prepare high-quality LHP/chalcogenide core/shell NCs, which possess great potential in the fabrication of stable optoelectronic devices.
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