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Reduced graphene oxide (RGO)-supported NiCo₂O₄ nanoparticles: an electrocatalyst for methanol oxidation.

Authors :
Das AK
Layek RK
Kim NH
Jung D
Lee JH
Source :
Nanoscale [Nanoscale] 2014 Sep 21; Vol. 6 (18), pp. 10657-65. Date of Electronic Publication: 2014 Aug 04.
Publication Year :
2014

Abstract

The design and development of cheap, highly active, and durable non-platinum (Pt)-based electrocatalysts for methanol electrooxidation is highly desirable, but is a challenging task. In this paper, we demonstrate the application of a hydrothermally synthesized NiCo₂O₄-reduced graphene oxide (RGO) composite as an electrocatalyst for the electrochemical oxidation of methanol in alkaline pH. The physicochemical properties of the NiCo₂O₄-RGO composite were investigated via Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), Raman spectroscopy (RS), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) measurements. The physical characterization methods confirm the deposition of NiCo₂O₄ nanoparticles on the RGO surface. The TEM image shows that the NiCo₂O₄ nanoparticles with an average size of ∼10 nm are distributed over the RGO surface. Compared to RGO and NiCo₂O₄ nanoparticles, the NiCo₂O₄-RGO-based electrode shows excellent electrocatalytic activity for the oxidation of methanol in alkaline pH. On the NiCo₂O₄-RGO-based electrode, the oxidation of methanol occurs at ∼0.6 V with a higher catalytic current density, and the response is highly stable. The excellent electrocatalytic activity of the NiCo₂O₄-RGO composite is attributed to the synergistic effects between the NiCo₂O₄ nanoparticles and RGO. Since the NiCo₂O₄-RGO composite shows a highly stable response during methanol oxidation reaction, it is a very promising material to be used as an electrocatalyst in the development of high performance non-Pt based alkaline fuel cells.

Details

Language :
English
ISSN :
2040-3372
Volume :
6
Issue :
18
Database :
MEDLINE
Journal :
Nanoscale
Publication Type :
Academic Journal
Accession number :
25089926
Full Text :
https://doi.org/10.1039/c4nr02370f