Department of Molecular Chemistry and Material Science, Weizmann Institute of Science, Rehovot 7610001, Israel.
Department of Chemical Research Support, Weizmann Institute of Science, Rehovot 7610001, Israel.
Nano Lett. 2021 Dec 8;21(23):9916-9921. doi: 10.1021/acs.nanolett.1c03131. Epub 2021 Nov 23.
Colloidal inorganic nanofluorides have aroused great interest for various applications with their development greatly accelerated thanks to advanced synthetic approaches. Nevertheless, understanding their colloidal evolution and the factors that affect their dispersion could improve the ability to rationally design them. Here, using a multimodal approach that combines DLS, NMR, and cryogenic-TEM, we elucidate the formation dynamics of nanofluorides in water through a transient aggregative phase. Specifically, we demonstrate that ligand-cation interactions mediate a transient aggregation of as-formed CaF nanocrystals (NCs) which governs the kinetics of the colloids' evolution. These observations shed light on key stages through which CaF NCs are dispersed in water, highlighting fundamental aspects of nanofluorides formation mechanisms. Our findings emphasize the roles of ligands in NCs' synthesis beyond their function as surfactants, including their ability to mediate colloidal evolution by complexing cationic precursors, and should be considered in the design of other types of NCs.
胶体无机纳米氟化物因其先进的合成方法而得到了极大的发展,引起了人们对各种应用的极大兴趣。然而,了解它们的胶体演变以及影响它们分散的因素可以提高合理设计它们的能力。在这里,我们使用一种多模态方法,结合 DLS、NMR 和低温 TEM,通过瞬态聚集相阐明了纳米氟化物在水中的形成动力学。具体来说,我们证明配体-阳离子相互作用介导了形成的 CaF 纳米晶体 (NCs) 的瞬态聚集,这控制了胶体演变的动力学。这些观察结果揭示了 CaF NCs 在水中分散的关键阶段,强调了纳米氟化物形成机制的基本方面。我们的发现强调了配体在 NCs 合成中的作用超出了它们作为表面活性剂的功能,包括它们通过与阳离子前体配位来介导胶体演变的能力,这在设计其他类型的 NCs 时应予以考虑。