Collantes Cynthia, González Pedro Victoria, Bañuls María-José, Maquieira Ángel
Instituto Interuniversitario de Investigación de Reconocimiento Molecular y Desarrollo Tecnológico (IDM), Universitat Politècnica de València-Universitat de València, Camino de Vera s/n, E46022 València, Spain.
Departamento de Química, Universitat Politècnica de València, Camino de Vera s/n, E46022 València, Spain.
ACS Appl Nano Mater. 2021 Feb 26;4(2):2011-2018. doi: 10.1021/acsanm.0c03340. Epub 2021 Feb 12.
Despite the rising advances in the field of metal halide perovskite nanocrystals (NCs), the exploitation of such nanoparticles as luminescent labels for imaging and biosensing is still unclear and in the early stages of investigation. One of the major challenges toward the implementation of metal halide perovskite NCs in biosensing applications is to produce monodispersed nanoparticles with desired surface characteristics and compatible with aqueous environments. Here, we report the synthesis of monodispersed spherical CsPbBr@SiO core-shell nanoparticles by post-synthetic chemical transformation of 3D CsPbBr NCs in the presence of tetraethyl orthosilicate and a critical water/ammonia ratio. This method involves an ammonia-mediated and ammonia-induced "top-down" transformation of as-synthesized 3D CsPbBr NCs to smaller CsPb2Br5 nanoclusters (ca. 2-3 nm), which trigger a seed-mediated silica growth, yielding monodispersed spherical blue luminescent (λ = 432 nm) CsPbBr@SiO perovskite nanoparticles. By adjusting the reaction conditions, core-shell nanoparticles of a 36.1 ± 4.5 nm diameter, which preserve their optical properties in water, were obtained. Besides that, the viability of the developed nanoparticles as a luminescent label for biosensing has been proven by specific biorecognition of the IgG protein in a direct immunoassay. Our work sheds light on the chemical processes and transformations involved in the silica nucleation mechanism in the presence of perovskite nanoparticles and opens the way for the future rational design of the next generation of semiconductor NC luminescent biological labels.
尽管金属卤化物钙钛矿纳米晶体(NCs)领域取得了不断进展,但将此类纳米颗粒用作成像和生物传感的发光标记物的开发仍不明确,尚处于研究初期。在生物传感应用中实现金属卤化物钙钛矿NCs面临的主要挑战之一是制备具有所需表面特性且与水性环境兼容的单分散纳米颗粒。在此,我们报告了通过在原硅酸四乙酯和临界水/氨比存在下对3D CsPbBr NCs进行合成后化学转化,合成单分散球形CsPbBr@SiO核壳纳米颗粒。该方法涉及氨介导和氨诱导的将合成的3D CsPbBr NCs “自上而下” 转化为更小的CsPb2Br5纳米团簇(约2 - 3 nm),这些纳米团簇引发种子介导的二氧化硅生长,产生单分散球形蓝色发光(λ = 432 nm)的CsPbBr@SiO钙钛矿纳米颗粒。通过调整反应条件,获得了直径为36.1 ± 4.5 nm的核壳纳米颗粒,其在水中保留了光学性质。此外,通过在直接免疫分析中对IgG蛋白的特异性生物识别,证明了所开发的纳米颗粒作为生物传感发光标记物的可行性。我们的工作揭示了在钙钛矿纳米颗粒存在下二氧化硅成核机制中涉及的化学过程和转化,为下一代半导体NC发光生物标记物的未来合理设计开辟了道路。