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Following the Formation of Silver Nanoparticles Using In Situ X-ray Absorption Spectroscopy

[Image: see text] The formation of silver and Au@Ag core@shell nanoparticles via reduction of AgNO(3) by trisodium citrate was followed using in situ X-ray absorption near-edge structure (XANES) spectroscopy and time-resolved UV–visible (UV–vis) spectroscopy. The XANES data were analyzed through lin...

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Detalles Bibliográficos
Autores principales: Godfrey, Ian J., Dent, Andrew J., Parkin, Ivan P., Maenosono, Shinya, Sankar, Gopinathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7301364/
https://www.ncbi.nlm.nih.gov/pubmed/32566831
http://dx.doi.org/10.1021/acsomega.0c00697
Descripción
Sumario:[Image: see text] The formation of silver and Au@Ag core@shell nanoparticles via reduction of AgNO(3) by trisodium citrate was followed using in situ X-ray absorption near-edge structure (XANES) spectroscopy and time-resolved UV–visible (UV–vis) spectroscopy. The XANES data were analyzed through linear combination fitting, and the reaction kinetics were found to be consistent with first-order behavior with respect to silver cations. For the Au@Ag nanoparticles, the UV–vis data of a lab-scale reaction showed a gradual shift in dominance between the gold- and silver-localized surface plasmon absorbance bands. Notably, throughout much of the reaction, distinct gold and silver contributions to the UV–vis spectra were observed; however, in the final product, the contributions were not distinct.