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Erschienen in: Journal of Nanoparticle Research 11/2013

01.11.2013 | Research Paper

The synthesis and arrested oxidation of amorphous cobalt nanoparticles using DMSO as a functional solvent

verfasst von: Jennifer N. Duggan, Michael J. Bozack, Christopher B. Roberts

Erschienen in: Journal of Nanoparticle Research | Ausgabe 11/2013

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Abstract

Magnetic nanoparticles exhibit a strong tendency to become overly oxidized and unstable during synthesis, ultimately leading to nanoparticle agglomeration and degradation. Capping agents can be used during nanoparticle synthesis to provide particle surface coverage and to improve nanoparticle dispersibility in solution, while preventing excessive oxidation and agglomeration. This paper presents a technique to synthesize amorphous 3.7 ± 1.5 nm cobalt (Co) nanoparticles using dimethyl sulfoxide (DMSO) to function as both the stabilizing agent and the solvent for Co nanoparticles via a quick, solvent-based reduction of Co2+ with NaBH4 in a DMSO solvent. UV–visible spectroscopy analysis was used to determine the minimum amount of reducing agent needed to produce Co nanoparticles so as to limit the waste of reagents. TEM and SEM imaging were used to study the morphology of the Co nanoparticles from the DMSO dispersion and of the Co nanoparticle powder. FT-IR was used to elucidate the nature of the interaction between the Co nanoparticle surface and DMSO. Furthermore, SEM–EDS elemental mapping was used to determine the composition and surface properties of the Co nanoparticles. This synthesis method demonstrates that Co nanoparticles can be successfully synthesized by simply using DMSO as a functional solvent, thereby avoiding excessive oxidation and agglomeration in solution.

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Metadaten
Titel
The synthesis and arrested oxidation of amorphous cobalt nanoparticles using DMSO as a functional solvent
verfasst von
Jennifer N. Duggan
Michael J. Bozack
Christopher B. Roberts
Publikationsdatum
01.11.2013
Verlag
Springer Netherlands
Erschienen in
Journal of Nanoparticle Research / Ausgabe 11/2013
Print ISSN: 1388-0764
Elektronische ISSN: 1572-896X
DOI
https://doi.org/10.1007/s11051-013-2089-0

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