Electrocatalytic oxidation of methanol at nanoparticle-based MnOx/NiOx/Pt ternary catalysts: Optimization of loading level and order of deposition

Mohammad, Ahmad M.; El-Nowihy, Ghada H.; Khalil, M.M.H.; El-Deab, Mohamed S.;

Abstract


A nanoparticle-based ternary catalyst composed of Pt (nano-Pt), nickel oxide (nano-NiOx) and manganese oxide (nano-MnOx), all were assembled on a glassy carbon (GC) substrate, was developed for the direct methanol electro-oxidation reaction (MOR) in an alkaline medium. The electrocatalytic activity of the modified electrodes toward MOR depended on the loading level of nano-Pt, nano-NiOx and nano-MnOx onto the GC electrode. Moreover, the order of deposition of nano-NiOx and nano-MnOx has critically influenced the catalytic activity and stability of MOR. The highest electrocatalytic activity was obtained at the MnOx/NiOx/Pt/GC electrode with nano-Pt directly deposited onto the GC surface followed by nano-NiOx and nano-MnOx sequentially. The catalytic activity of MOR at this electrode was about five times higher than that obtained at Pt/GC electrode. The stability and the effect of the operating pH on the catalytic activity of the proposed catalyst were investigated. Several techniques such as the cyclic voltammetry, field-emission scanning electron microscopy and energy dispersive X-ray spectroscopy (EDS) were used to address the catalytic activity of the catalyst and to reveal its surface morphology and bulk composition.


Other data

Title Electrocatalytic oxidation of methanol at nanoparticle-based MnOx/NiOx/Pt ternary catalysts: Optimization of loading level and order of deposition
Authors Mohammad, Ahmad M.; El-Nowihy, Ghada H.; Khalil, M.M.H. ; El-Deab, Mohamed S.
Keywords ALKALINE MEDIA; ELECTRODES; ELECTROCHEMISTRY; MECHANISM; BEHAVIOR; SULFIDE; OXIDES; SENSOR; OXYGEN; MNO2
Issue Date 1-Jan-2015
Publisher ELECTROCHEMICAL SOC INC
Journal Journal of The Electrochemical Society 
Volume 161
Issue 14
Start page F1340
End page F1347
ISSN 00134651
DOI 10.1149/2.0181414jes
Scopus ID 2-s2.0-84923367504
Web of science ID WOS:000345975500083

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