Department of Chemistry, University of Copenhagen, Universitetsparken 5, 2100 Copenhagen Ø, Denmark.
School of Mathematics and Science, Department of Chemistry, Carl von Ossietzky University of Oldenburg, 26111 Oldenburg, Germany.
J Phys Chem Lett. 2021 Apr 1;12(12):3224-3231. doi: 10.1021/acs.jpclett.1c00241. Epub 2021 Mar 25.
Understanding the formation of nanomaterials down to the atomic level is key to rational design of advanced materials. Despite their widespread use and intensive study over the years, the detailed formation mechanism of platinum (Pt) nanoparticles remains challenging to explore and rationalize. Here, various characterization techniques, and in particular X-ray total scattering with pair distribution function (PDF) analysis, are used to follow the structural and chemical changes taking place during a surfactant-free synthesis of Pt nanoparticles in alkaline methanol. Polynuclear structures form at the beginning of the synthesis, and Pt-Pt pair distances are identified before any nanoparticles are generated. The structural motifs best describing the species formed change with time, e.g., from [PtCl-PtCl] and [PtCl-PtCl-PtCl] to [PtCl-PtCl-PtCl]. The formation of these polynuclear structures with Pt-Pt coordination before the formation of the nanoparticles is suggested to account for the fast nucleation observed in the synthesis.
深入了解纳米材料的原子水平结构对于合理设计先进材料至关重要。尽管多年来它们被广泛应用并进行了深入研究,但铂(Pt)纳米颗粒的详细形成机制仍然难以探索和合理化。在这里,各种表征技术,特别是带有配对分布函数(PDF)分析的 X 射线总散射,用于跟踪在碱性甲醇中无表面活性剂合成 Pt 纳米颗粒过程中发生的结构和化学变化。在合成开始时形成多核结构,并且在生成任何纳米颗粒之前确定 Pt-Pt 键距离。描述形成物种的结构基序随时间变化,例如,从[PtCl-PtCl]和[PtCl-PtCl-PtCl]变为[PtCl-PtCl-PtCl]。形成这些具有 Pt-Pt 配位的多核结构,然后才形成纳米颗粒,这被认为可以解释在合成中观察到的快速成核。