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Preparation of cobalt oxide catalysts on stainless steel wire mesh by combination of magnetron sputtering and electrochemical deposition

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    0517382 - FZÚ 2020 RIV NL eng J - Journal Article
    Dvořáková, M. - Perekrestov, Roman - Kšírová, P. - Balabánová, Jana - Jirátová, Květa - Maixner, J. - Topka, Pavel - Rathouský, Jiří - Koštejn, Martin - Čada, Martin - Hubička, Zdeněk - Kovanda, F.
    Preparation of cobalt oxide catalysts on stainless steel wire mesh by combination of magnetron sputtering and electrochemical deposition.
    Catalysis Today. Roč. 334, Aug (2019), s. 13-23. ISSN 0920-5861. E-ISSN 1873-4308
    R&D Projects: GA ČR GA17-08389S; GA MŠMT(CZ) EF16_013/0001821
    Institutional support: RVO:68378271 ; RVO:61388955 ; RVO:67985858
    Keywords : cobalt oxide * plasma sputtering * electrochemical deposition * supported catalysts * deep ethanol oxidation
    OECD category: Chemical process engineering; Chemical process engineering (UCHP-M); Physical chemistry (UFCH-W)
    Impact factor: 5.825, year: 2019
    Method of publishing: Limited access
    https://doi.org/10.1016/j.cattod.2019.03.008

    Supported catalysts with Co3O4 deposited on stainless steel wire meshes were prepared and examined in the total oxidation of ethanol. Combination of reactive magnetron sputtering of cobalt particles in oxidation Ar+O2 atmosphere and electrochemical formation of cobalt hydroxide precursors using cathodic reduction of cobalt nitrate in aqueous solution was applied for coating of the supports the precursors were then transformed to Co3O4 by subsequent heating at 500 °C in air. Two plasma enhanced PVD methods, namely the radio-frequency (RF) magnetron sputtering and high-power impulse magnetron sputtering (HiPIMS) were used for obtaining of Co3O4 thin films. The catalysts prepared using RF magnetron sputtering were more active than analogous catalysts prepared using the HiPIMS process. The catalyst obtained by electrochemical deposition on a bare stainless steel mesh had the highest Co3O4 loading and showed the highest efficiency in total ethanol oxidation.

    Permanent Link: http://hdl.handle.net/11104/0302706

     
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