Kinetic study of CO oxidation on clean and oxidized Pt

dc.contributor.authorDahlstro̸m, Per K.
dc.contributor.authorHarrington, David A.
dc.contributor.authorSeland, F.
dc.date.accessioned2019-06-27T15:25:25Z
dc.date.available2019-06-27T15:25:25Z
dc.date.copyright2012en_US
dc.date.issued2012
dc.description.abstractBulk CO oxidation on smooth polycrystalline platinum was studied with a rotating disk electrode and cyclic voltammetry in CO-saturated 0.5 M sulfuric acid. The reaction rate was modelled with differential equations. The modelling goal was to build a model that reproduces the experimental current–potential characteristics, with special attention to the platinum oxide region. Two different models were tested: one containing conventional chemical and electrochemical reaction steps, and one built around an empirical equation describing the rate of platinum oxide formation and reduction. The latter model produced good fits to the experimental results. Both models showed that CO oxidation in the platinum oxide range proceeds via direct reaction between an adsorbed species such as PtOH and dissolved CO.en_US
dc.description.reviewstatusRevieweden_US
dc.description.scholarlevelFacultyen_US
dc.description.sponsorshipThe Natural Sciences and Engineering Research Council of Canada, University of Victoria, and Norwegian University of Science and Technology (NTNU) are gratefully acknowledged for financial support.en_US
dc.identifier.citationDahlstrøm, P.K., Harrington, D.A. & Seland, F. (2012). Kinetic study of CO oxidation on clean and oxidized Pt. Electrochimica Acta, 82, 550-557. https://doi.org/10.1016/j.electacta.2012.04.150en_US
dc.identifier.urihttps://doi.org/10.1016/j.electacta.2012.04.150
dc.identifier.urihttp://hdl.handle.net/1828/10940
dc.language.isoenen_US
dc.publisherElectrochimica Actaen_US
dc.subjectCO oxidationen_US
dc.subjectPlatinumen_US
dc.subjectOxideen_US
dc.subjectRDEen_US
dc.subjectKinetic modelen_US
dc.titleKinetic study of CO oxidation on clean and oxidized Pten_US
dc.typePostprinten_US

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