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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