在抗溶剂中一步合成用于生物成像的高荧光过氧化物纳米晶体

Peuli Nath, Aniruddha Ray
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摘要

所有无机过氧化物纳米晶体(CsPbX3 NCs)都具有优异的光学特性,量子产率高,吸收和发射光谱尺寸可调,因此应用广泛。所有常用的合成技术,如热注入法和配体辅助再沉淀法(LARP),都使用二甲基甲酰胺、二甲亚砜或十八烯等 "优质 "溶剂来溶解前体盐。在热混合物中快速注入溶解的前驱体盐(热注入法),或在 "差 "溶剂中加入 "好 "溶剂(LARP 法)诱导结晶,都会引发 CsPbX3 NCs 的形成。在这里,我们提出了一种在反溶剂系统中代替 "好 "溶剂合成 CsPbX3 包晶石纳米晶体的替代方法。通过添加微量的水诱导反溶剂中的结晶,从而形成高亮度的 CsPbX3 纳米晶体。通过这种方法,光致发光量子产率最高可达 91%。此外,这些 CsPbBr3 NCs 还可以与二氧化硅等聚合物在同一锅中进行改性,形成核壳结构。与裸露的 NCs 相比,将 NCs 封装在二氧化硅保护壳中可大大提高其水稳定性。二氧化硅包覆的 CsPbBr3 NCs 在水中显示出强烈的荧光,被用来标记乳腺癌细胞,从而证明了它作为光学对比剂在先进生物成像应用中的潜力。总之,这种合成方法所需的步骤和时间最少,而且可以在环境气氛中进行,从而提高了其通用性和实用性,这在资源匮乏的环境中尤其具有吸引力。
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One-step synthesis of highly fluorescent perovskite nanocrystals in antisolvent for bioimaging
All inorganic perovskite nanocrystals (CsPbX3 NCs) have excellent optical properties with high quantum yield, size tunable absorption and emission spectra which makes them popular for a wide variety of applications. All the commonly used synthesis techniques, such as hot injection and ligand assisted reprecipitation method (LARP), use ‘good’ solvent such as dimethyl formamide, dimethyl sulfoxide or octadecene to dissolve the precursor salts. The CsPbX3 NCs formation is triggered either by rapid injection of the dissolved precursor salt in hot mixture (hot injection) or by adding a ‘good’ solvent into a ‘poor’ solvent (LARP) that induces crystallization. Here, we present an alternative synthesis of CsPbX3 perovskite nanocrystals in an antisolvent system, instead of a ‘good’ solvent. Crystallization in the antisolvent is induced by adding a trace amount of water, leading to the formation of highly bright CsPbX3 nanocrystals. This method resulted in a maximum photoluminescent quantum yield of ∼91%. Furthermore, these CsPbBr3 NCs can be modified to create core–shell structures with polymers such as silica, in the same pot. Encapsulating the NCs within a protective silica shell resulted in vastly superior water stability compared to the bare NCs. The silica coated CsPbBr3 NCs showed strong fluorescence in water were used to label breast cancer cells, thereby demonstrating its potential as an optical contrast agent for advanced bioimaging applications. Overall, this synthesis approach requires minimal steps and time, and can be carried out in an ambient atmosphere, thereby increasing its versatility and practicality, which is particularly attractive in low-resource settings.
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