Title:
A comparative study of electrocatalytic performance of metal molybdates for the water oxidation

dc.contributor.authorV.K.V.P. Srirapu
dc.contributor.authorAjay Kumar
dc.contributor.authorNirmala Kumari
dc.contributor.authorPankaj Srivastava
dc.contributor.authorRavindra Nath Singh
dc.date.accessioned2026-02-07T08:45:16Z
dc.date.issued2018
dc.description.abstractBinary mixed oxides of molybdenum and a metal of the first-row transition metals with compositional formulae, MMoO4 (where M = Cr, Fe, Mn, Co, Ni, Cu or Zn), were prepared by a microwave-assisted co-precipitation method and their electrocatalytic activities have been investigated for oxygen evolution reaction (OER) in 1 M KOH. Materials were characterized for structural and electrocatalytic surface properties using FT-IR, XRD, TEM, BET, XPS, cyclic voltammetry (CV) and anodic Tafel polarization techniques. The crystallite size of oxides ranged between ∼17 and ∼41 nm. For electrochemical studies, oxides obtained in powders form were produced in the thin-film form on the pretreated glassy carbon (GC) support. It has been observed that among electrocatalysts investigated, the CoMoO4/GC electrode was the greatest OER active while that the MnMoO4/GC electrode was the least active. The OER produced low Tafel slopes, ∼36, ∼43 and ∼46 mV respectively on FeMoO4, CoMoO4 and CuMoO4 while it showed the higher Tafel slopes on CrMoO4(∼57 mV), NiMoO4(∼71 mV) and MnMoO4 (∼89 mV). © 2018 Hydrogen Energy Publications LLC
dc.identifier.doi10.1016/j.ijhydene.2018.07.060
dc.identifier.issn3603199
dc.identifier.urihttps://doi.org/10.1016/j.ijhydene.2018.07.060
dc.identifier.urihttps://dl.bhu.ac.in/bhuir/handle/123456789/31915
dc.publisherElsevier Ltd
dc.subjectElectrocatalysis
dc.subjectElectrocatalytic activity
dc.subjectMetal molybdate electrocatalysts
dc.subjectMicrowave-assisted co-precipitation method
dc.subjectOxygen evolution
dc.titleA comparative study of electrocatalytic performance of metal molybdates for the water oxidation
dc.typePublication
dspace.entity.typeArticle

Files

Collections