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Local structure of Co doped RuO2 nanocrystalline electrocatalytic materials for chlorine and oxygen evolution

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    SYSNO ASEP0434971
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleLocal structure of Co doped RuO2 nanocrystalline electrocatalytic materials for chlorine and oxygen evolution
    Author(s) Petrykin, Valery (UFCH-W)
    Macounová, Kateřina (UFCH-W) RID
    Okube, Maki (UFCH-W)
    Mukerjee, S. (US)
    Krtil, Petr (UFCH-W) RID, ORCID
    Source TitleCatalysis Today. - : Elsevier - ISSN 0920-5861
    Roč. 202, MAR 2013 (2013), s. 63-69
    Number of pages7 s.
    Languageeng - English
    CountryNL - Netherlands
    Keywordsoxygen evolution ; chlorine evolution ; oxide
    Subject RIVCG - Electrochemistry
    R&D ProjectsIAA400400906 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    Institutional supportUFCH-W - RVO:61388955
    UT WOS000311939800009
    EID SCOPUS84870521003
    DOI https://doi.org/10.1016/j.cattod.2012.03.075
    AnnotationNano-particulate Co doped ruthenium dioxide electrocatalysts of the general formula Ru1-xCoxO2-y (0 < x 0.3) were prepared by a co-precipitation method. The electrocatalysts with x < 0.2 conform to a single phase nano-crystalline materials. On the local level the Co forms clusters dispersed in the original rutile-like matrix. The local environment of the Co conforms to a rutile model which preserves the cationic arrangement but suppresses the probability of the Ru-Ru and Co-Co neighbors along the shortest metal-metal bonds. The electrocatalytic activity of the synthesized Ru1-xCoxO2-y materials in oxygen evolution is comparable with that of the non-doped ruthenium dioxide and little depends on the actual Co content. In presence of chlorides the Co doped materials are more selective towards oxygen evolution compared with the non doped ruthenia. The enhanced oxygen evolution in the case of Co doped electrocatalysts can be attributed to a chemical recombination of surface confined oxo-species. The selectivity shift towards oxygen evolution can be linked with limited activity of the Ru1-xCoxO2-y materials in the chlorine evolution reaction which seems to be relatively weakly dependent on the chloride concentration. (C) 2012 Elsevier B.V. All rights reserved.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2015
Number of the records: 1  

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