聚结(物理)
纳米晶
原位
纳米材料
材料科学
纳米技术
纳米颗粒
化学物理
化学工程
单体
粒子(生态学)
密度泛函理论
化学
计算化学
聚合物
有机化学
物理
复合材料
工程类
地质学
海洋学
天体生物学
作者
Reut Mashiach,Haim Weissman,Liat Avram,Lothar Houben,Olga Brontvein,Anna Lavie,Vaishali Arunachalam,Michal Leskes,Boris Rybtchinski,Amnon Bar‐Shir
标识
DOI:10.1038/s41467-020-20512-6
摘要
Understanding inorganic nanocrystal (NC) growth dynamic pathways under their native fabrication environment remains a central goal of science, as it is crucial for rationalizing novel nanoformulations with desired architectures and functionalities. We here present an in-situ method for quantifying, in real time, NCs' size evolution at sub-nm resolution, their concentration, and reactants consumption rate for studying NC growth mechanisms. Analyzing sequential high-resolution liquid-state 19F-NMR spectra obtained in-situ and validating by ex-situ cryoTEM, we explore the growth evolution of fluoride-based NCs (CaF2 and SrF2) in water, without disturbing the synthesis conditions. We find that the same nanomaterial (CaF2) can grow by either a particle-coalescence or classical-growth mechanism, as regulated by the capping ligand, resulting in different crystallographic properties and functional features of the fabricated NC. The ability to reveal, in real time, mechanistic pathways at which NCs grow open unique opportunities for tunning the properties of functional materials.
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