钙钛矿(结构)
铕
量子点
表面改性
材料科学
密度泛函理论
发光
纳米技术
配体(生物化学)
光电子学
非阻塞I/O
化学
计算化学
物理化学
结晶学
催化作用
有机化学
生物化学
受体
作者
Pengfei Feng,Xiaoxi Yang,Xiaoxia Feng,Guodong Zhao,Xiaochen Li,Jing Cao,Yu Tang,Chun‐Hua Yan
出处
期刊:ACS Nano
[American Chemical Society]
日期:2021-02-25
卷期号:15 (4): 6266-6275
被引量:64
标识
DOI:10.1021/acsnano.0c09228
摘要
Inorganic perovskite quantum dots (QDs) have attracted great scientific attention in the field of luminescent materials, but the application has been limited by the inferior stability that results from highly dynamic capping ligands. In this work, we use a rare-earth complex to modify perovskite QDs with ligand exchange to realize perovskite functionalization; meanwhile, the stability of perovskite QDs is greatly improved. Density functional theory calculation results show that the adsorption energy of the europium complex to QDs is higher than that with traditional ligands, which provides a thermodynamic basis for stability improvement. Furthermore, the modified QDs exhibit attractive dual-response property, including temperature and pH response ascribed to QDs and europium complexes, respectively. The superior property can be applied to multi-stimuli-responsive optical encoding, which is further capable of enhancing the security of encrypted information. This study not only affords a strategy for the synthesis of highly stable perovskites but also provides a method for the functionalization of perovskites.
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