Pt4+ as an active site for oxygen evolution reaction in La1-xSrxCo1-yPtyO3

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dc.contributor.author Bisht, Anuj
dc.contributor.author Yadav, Pradeep Kumar
dc.contributor.author Dhakar, Shikha
dc.contributor.author Sharma, Sudhanshu
dc.coverage.spatial United States of America
dc.date.accessioned 2021-11-26T14:38:46Z
dc.date.available 2021-11-26T14:38:46Z
dc.date.issued 2021-11
dc.identifier.citation Bisht, Anuj; Yadav, Pradeep Kumar; Dhakar, Shikha and Sharma, Sudhanshu, “Pt4+ as an active site for oxygen evolution reaction in La1-xSrxCo1-yPtyO3”, The Journal of Physical Chemistry C, DOI: 10.1021/acs.jpcc.1c06426, vol. 125, no. 46, pp. 25488-25496, Nov. 2021. en_US
dc.identifier.issn 1932-7447
dc.identifier.issn 1932-7455
dc.identifier.uri https://doi.org/10.1021/acs.jpcc.1c06426
dc.identifier.uri https://repository.iitgn.ac.in/handle/123456789/7295
dc.description.abstract This study presents an investigation on the role of Pt4+ in Pt-doped La1?xSrxCoO3 (LSPtCO) perovskite for oxygen evolution reaction (OER) activity. LSPtCO with Pt in the +4 oxidation state shows the highest activity for OER in comparison to undoped La1?xSrxCoO3 (LSCO) and Pt metal-supported LSCO (Pt is in the zero oxidation state). These results indicate that a high oxidation state of Pt is favorable for the OER activity. Pt4+ is also shown as the active center for the OER reaction as its reductive treatment decreases the OER activity significantly. Thus, the formation of high-valent Pt is a key factor in fabricating an active OER catalyst. While Pt metal may not be a good catalyst for OER, Pt4+ is significantly superior, especially in LSCO
dc.description.statementofresponsibility by Anuj Bisht, Pradeep Kumar Yadav, Shikha Dhakar and Sudhanshu Sharma
dc.format.extent vol. 125, no. 46, pp. 25488-25496
dc.language.iso en_US en_US
dc.publisher American Chemical Society en_US
dc.subject LSPtCO en_US
dc.subject Oxygen Evolution Reaction (OER) en_US
dc.subject Pt4+ en_US
dc.subject LSCO en_US
dc.title Pt4+ as an active site for oxygen evolution reaction in La1-xSrxCo1-yPtyO3 en_US
dc.type Article en_US
dc.relation.journal The Journal of Physical Chemistry C


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