材料科学
光致发光
卤化物
水溶液
纳米晶
钙钛矿(结构)
溶解度
离子键合
化学工程
结晶
溶解
表面改性
发光
量子产额
纳米技术
无机化学
荧光
有机化学
化学
离子
光电子学
工程类
物理
量子力学
作者
Zha Li,Qingsong Hu,Zhifang Tan,Ying Yang,Meiying Leng,Xiuli Liu,Cong Ge,Liduo Wang,Jiang Tang
标识
DOI:10.1021/acsami.8b16471
摘要
Lead halide perovskite nanocrystals (NCs) have attracted intense attention because of their excellent optoelectronic properties. The ionic nature of halide perovskites makes them highly vulnerable to water. Encapsulation of perovskite NCs with inorganic or organic materials has been reported to enhance their stability; however, they often suffer from large aggregation size, low water solubility, and difficulty for further surface functionalization. Here, we report a facile aqueous process to synthesize water-soluble CsPbBr3/Cs4PbBr6 NCs with the assistance of a fluorocarbon agent (FCA), which features a novel mechanism of the perovskite crystallization at the oil/water interface and direct perovskite NCs/FCA self-assembly in an aqueous environment. The products exhibit a high absolute photoluminescence quantum yield (PLQY) of ∼80% in water with the PL lasting for weeks. Through successive ionic layer adsorption and reaction, BaSO4 was further applied to encapsulate the NCs, which greatly enhanced their stability in phosphate-buffered saline solutions. The high stability in water and saline solution, high PLQY, and tunable emission wavelength, together with the successful demonstration of brain tissue labeling and PL under X-ray excitation, make our perovskite NCs a promising choice for X-ray fluorescent biolabels.
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