Issue 22, 2014

A study on the synthesis of Ni50Co50 alloy nanostructures with tuned morphology through metal–organic chemical routes

Abstract

NiCo bimetallic nanostructures with various morphologies have been synthesized using a broad range of solvents, surfactants and precursors that are available in the metal–organic chemical toolbox. Polygonal particles, nanowires and isotropic nanospheres have been obtained, among others. We describe the chemical pathways to achieve anisotropic growth either by an ‘in situ’ seed-mediated approach or by simply selecting suitable reaction media and growth modifiers. We describe the role of a variety of synthetic factors that influence the final shape of such an alloy material at the nanoscale. The alloying between cobalt and nickel is evidenced by XRD and HRTEM techniques. Room-temperature ferromagnetic behavior is observed for NiCo nanoparticles and high values for saturation magnetization and coercivity are recorded by SQuID magnetometry. The saturation magnetization value for the NiCo nanostructures is typically set between the corresponding “bulk” ones of cobalt and nickel metals. It is always comparable to the suggested value of the Ni50Co50 bulk alloy. The synthetic protocols derived from our extensive study are quantitative and versatile, allowing high reaction yields. Although macroscopic characterization techniques evidence the presence of a stoichiometric NiCo alloy, we show that in certain cases nanoscale characterization analyses are also needed for a more accurate evaluation of the alloy composition at the atomic level.

Graphical abstract: A study on the synthesis of Ni50Co50 alloy nanostructures with tuned morphology through metal–organic chemical routes

Supplementary files

Article information

Article type
Paper
Submitted
06 Feb 2014
Accepted
24 Mar 2014
First published
24 Mar 2014

Dalton Trans., 2014,43, 8469-8479

Author version available

A study on the synthesis of Ni50Co50 alloy nanostructures with tuned morphology through metal–organic chemical routes

S. Mourdikoudis, V. Collière, P. Fau and M. L. Kahn, Dalton Trans., 2014, 43, 8469 DOI: 10.1039/C4DT00390J

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