Issue 32, 2022

Co-digestive ripening assisted phase-controlled synthesis of Ag–Sn intermetallic nanoparticles and their dye degradation activity

Abstract

The Ag–Sn based system in the nano-size regime is one of the strongest candidates for lead-free solders. Besides, the investigation of several other applications of Ag–Sn nanostructures, especially in catalysis, remains scarce which makes it an interesting system to synthesize and explore its chemistry. In this report, nearly monodisperse ε-Ag3Sn intermetallic nanoparticles were prepared by a simple and convenient solution-based process of co-digestive ripening using Ag and Sn colloids obtained by the solvated metal atom dispersion (SMAD) method. Optimization of the temperature and stoichiometric ratio between the metal elements and the use of an appropriate capping agent are crucial factors to realise phase pure intermetallic nanoparticles. Ag3Sn nanoparticles with a size of 3.8 nm ± 0.6 nm were obtained within 12 h of reaction when tri-n-octylphosphine/tri-n-octylphosphine oxide was used as the capping agent at 205 °C. Interestingly, Ag3Sn@SnOx core–shell nanostructures were obtained by changing the capping agent to palmitic acid. These nanostructures were thoroughly characterized by powder X-ray diffraction, transmission electron microscopy (TEM and STEM-EDS), X-ray photoelectron spectroscopy and optical spectroscopy. Thereafter, Ag and Ag3Sn nanoparticles were utilized for photocatalytic degradation of methylene blue, methyl orange and a mixture of both the dyes.

Graphical abstract: Co-digestive ripening assisted phase-controlled synthesis of Ag–Sn intermetallic nanoparticles and their dye degradation activity

Supplementary files

Article information

Article type
Paper
Submitted
09 May 2022
Accepted
11 Jul 2022
First published
11 Jul 2022

Dalton Trans., 2022,51, 12147-12160

Co-digestive ripening assisted phase-controlled synthesis of Ag–Sn intermetallic nanoparticles and their dye degradation activity

G. Bhatia and B. R. Jagirdar, Dalton Trans., 2022, 51, 12147 DOI: 10.1039/D2DT01438F

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