| Literature DB >> 33764071 |
Jette K Mathiesen1, Jonathan Quinson1, Alexandra Dworzak2,3, Tom Vosch1, Mikkel Juelsholt1, Emil T S Kjær1, Johanna Schröder4, Jacob J K Kirkensgaard5, Mehtap Oezaslan2,3, Matthias Arenz4, Kirsten M Ø Jensen1.
Abstract
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 in situ 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 [PtCl5-PtCl5] and [PtCl6-Pt2Cl6-PtCl6] to [Pt2Cl10-Pt3Cl8-Pt2Cl10]. 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.Entities:
Year: 2021 PMID: 33764071 DOI: 10.1021/acs.jpclett.1c00241
Source DB: PubMed Journal: J Phys Chem Lett ISSN: 1948-7185 Impact factor: 6.475