Eco-friendly synthesis and morphology-dependent superior electrocatalytic properties of CuS nanostructures

Copper sulfide with desired structure is of special interest for electrocatalytical application due to their unique physicochemical properties, simple synthesis and less toxic in nature. In this study, simple and eco-friendly (without using any template or surfactant) route for the fabrication of co...

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Veröffentlicht in:Electrochimica acta 2017-08, Vol.246, p.544-552
Hauptverfasser: Venkadesh, A., Radhakrishnan, S., Mathiyarasu, J.
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Sprache:eng
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Zusammenfassung:Copper sulfide with desired structure is of special interest for electrocatalytical application due to their unique physicochemical properties, simple synthesis and less toxic in nature. In this study, simple and eco-friendly (without using any template or surfactant) route for the fabrication of copper sulfide nanostructure morphologies were tuned from cauliflower, microflower to nanoparticles inter-connected network-like structures by changing the polarity of solvent medium during solvothermal synthesis. However, to the best of our knowledge, no such kinds of special three types of CuS nanostructure with excellent electro-catalytic properties using only H2O and C2H5OH as the solvents have been reported in the literature. The as-prepared different CuS nanostructure was characterized using FE-SEM, HR-TEM, XRD, XPS and cyclic voltammetry. This morphological alteration able to produce several precise nanostructures with improved electrocatalytic properties that led to an excellent performance towards enzymeless glucose oxidation. The CuS inter-connected nanoparticles modified electrode displayed a synergistic effect towards the oxidation of glucose (ipa: 103±5μA) when compared to that of cauliflower (ipa: 68±3.7μA) and microflower (ipa: 60±2.4μA) modified electrode surfaces. Further, the CuS inter-connected nanoparticles modified electrode showed a wide linear range (2.0×10−5−2.5×10−3M), high sensitivity (1085μAmM−1cm−2), low detection limit (2μM), rapid response time (
ISSN:0013-4686
1873-3859
DOI:10.1016/j.electacta.2017.06.077