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X-ray and optical characterization of the intermediate products in the Au3+ reduction process by oleylamine.

Authors :
Kirichkov, Mikhail V.
Guda, Alexander A.
Budnyk, Andriy P.
Bugaev, Aram L.
Lastovina, Tatiana A.
Shapovalov, Victor V.
Guda, Sergey A.
Trigub, Alexander L.
Rusalev, Yuri V.
Chernyshev, Anatoly V.
Lamberti, Carlo
Soldatov, Alexander V.
Source :
Radiation Physics & Chemistry. Oct2020, Vol. 175, pN.PAG-N.PAG. 1p.
Publication Year :
2020

Abstract

Formation of gold nanoparticles (NPs) from the mixture containing NaAuCl 4 as a precursor, octadecene as a solvent and oleylamine as a reducing agent was studied in situ by means of optical and X-ray spectroscopies. Dynamic light scattering (DLS) revealed the presence of initial aggregates of 500 nm average size which split into nanoparticles of about 8 nm width shortly after the reduction from Au3+ to Au+ has been completed. Based on Density Functional Theory (DFT) simulations and analysis of X-ray absorption spectra (XAS) we identified the structure of Au3+ and Au+ gold complexes. Quantitative analysis shows that Au NPs formation proceeds in following steps: substitution of chlorine ligands in Au3+ complex by four oleylamines; reduction of Au3+ to Au+ coordinated by two oleylamines. Latter process occurs in oleylamine micelles in octadecene. The third step is a fragmentation of large micelles into smaller ones shortly after reduction Au3+ to Au+, and subsequent slow growth of Au NPs via reduction of Au+ to Au0. • Initial agglomerates are split into small 8 nm particles during the reduction of Au. • Au(III) complex is coordinated by four N located at 2.04 Å. • Au(I) complex is coordinated by two N atoms at 2.05 Å. • No Cl atoms are present in the first coordination of Au at all stages of nanoparticle formation. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0969806X
Volume :
175
Database :
Academic Search Index
Journal :
Radiation Physics & Chemistry
Publication Type :
Academic Journal
Accession number :
143893745
Full Text :
https://doi.org/10.1016/j.radphyschem.2018.11.021