Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/63019
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dc.contributor.authorLal, Basant-
dc.contributor.authorGangwar, Brajesh-
dc.contributor.authorChauhan, Pankaj-
dc.date.accessioned2023-12-20T09:31:23Z-
dc.date.available2023-12-20T09:31:23Z-
dc.date.issued2023-12-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/63019-
dc.description1298-1302en_US
dc.description.abstractSpinel-type cobalt oxide (Co3O4) was prepared by the span-60 sol-gel (SSG) method by using cobalt nitrates and span-60 and characterized by FT-IR, XRD and SEM techniques and its catalytic performance for electrochemical formation of oxygen in a basic medium is investigated. For electrochemical studies, cyclic voltammetry and Tafel polarisation techniques were employed and the observed results of investigation showed that the Co3O4 electrode possessed higher value of oxide roughness factor and hence have improved electrocatalytic activity for the oxygen evolution process (OER) in basic solution. The Tafel slope at low over potential and order of reaction with regards to the variation of [OH ] concentration were found to be 73 mVdec–1 and (~1), respectively. The thermodynamic parameters such as standard electrochemical activation energy estimated from the Arrhenius plot and entropy of reaction were 35 kJmol–1 and 259 Jdeg–1mol–1for the OER. Highly negative value of entropy of the reaction indicated that electrocatalytic oxygen evolution by splitting water occurs via the mechanism involving the adsorption of reaction intermediate at the electrode surface.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR, Indiaen_US
dc.sourceIJC Vol.62(12) [December 2023]en_US
dc.subjectSol-gel combustion synthesisen_US
dc.subjectSpan-60en_US
dc.subjectTafel polarisationen_US
dc.subjectOERen_US
dc.subjectCyclic voltammetryen_US
dc.titleElectrocatalytic activity of Ni/Co3O4 obtained by span-60 sol-gel route for oxygen evolution in 1M KOH at 25°Cen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v62i12.5901en_US
Appears in Collections:IJC Vol.62(12) [December 2023]

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