Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/444
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dc.contributor.authorP. Paunovic, O. Popovski, A. Dimitrov, D. Slavkov, E. Lefterova, S. Hadzi Jordanoven_US
dc.date.accessioned2018-10-28T11:19:23Z-
dc.date.available2018-10-28T11:19:23Z-
dc.date.issued2007-04-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/444-
dc.description.abstractStructural and electrochemical characteristics of hypo–hyper d-electrocatalytic materials aimed for preparation of electrodes for hydrogen evolution were studied. The basic catalytic material was prepared of 10% amorphous Co (grain size <2 nm), 18% amorphous TiO2 and Vulcan XC-72, by sol–gel procedure. A number of modifications were applied aimed at improving the materials performances: (i) TiO2 was transformed into anatase by heating at 480 ◦C for 1 h, (ii) multiwalled carbon nanotubes (MWCNT) were used as a catalyst support instead of Vulcan XC-72 and (iii) Mo was added to Co phase in a quantity of 25 at.% (Mo:Co = 1:3). Both, material’s intrinsic catalytic activity and surface area were affected by these modifications. As a result, the electrocatalytic activity for hydrogen evolution was improved, e.g. transformation of TiO2 into anatase form lowers the HER overpotential (η) for 15mV at 60mAcm−2. Introduction of MWCNTs lowered η for 30mV, while addition of Mo to metallic phase for 40mV. The complete modification of all three catalyst’s components (10% MoCo3 + 18% anatase + MWCNTs) was the most effective with 60mV decrease of overpotential. Characterization was made by XRD, SEM, IR and XPS methods. Surface area was measured by means of cyclic voltammetry.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofElectrochimica Actaen_US
dc.titleStudy of structural and electrochemical characteristics of Co-based hypo–hyper d-electrocatalysts for hydrogen evolutionen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.electacta.2007.01.053-
item.grantfulltextopen-
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Appears in Collections:Faculty of Technology and Metallurgy: Journal Articles
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