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dc.contributor.authorReksten, Anita
dc.contributor.authorRussel, Andrea E.
dc.contributor.authorRichardson, Peter W.
dc.contributor.authorThompson, Stephen J.
dc.contributor.authorMathisen, Karina
dc.contributor.authorSeland, Frode
dc.contributor.authorSunde, Svein
dc.date.accessioned2020-04-03T11:44:43Z
dc.date.available2020-04-03T11:44:43Z
dc.date.created2020-01-09T20:43:19Z
dc.date.issued2019
dc.identifier.citationPhysical Chemistry, Chemical Physics - PCCP. 2019, 21 12217-12230.en_US
dc.identifier.issn1463-9076
dc.identifier.urihttps://hdl.handle.net/11250/2650335
dc.description.abstractIridium and ruthenium oxide are active electrocatalysts for oxygen evolution. The relation between preparation method, structure, and behavior of mixed oxides of iridium and ruthenium are of interest in order to obtain active and stable catalysts. In this work the structure of mixed Ru–Ir oxides synthesized by the polymeric precursor method, which involves the formation of a gel containing the metal precursors and subsequent heat-treatment in air, was studied for the IrxRu1−xO2 system. An in-depth analysis of X-ray diffraction (XRD) and X-ray absorption (XAS) data, including EXAFS and linear combination of XANES, shows that the polymeric precursor synthesis method is capable of providing an intimate mixing of Ir and Ru in the catalyst. In addition to the oxide phase, metal phases, i.e. with Ru or Ir or both in oxidation state zero (Ir(fcc) and Ru(hcp)), were also found in the product materials. Facing complex structures such as some of those synthesized here, we have shown that a representation of shells with more than one atom type are efficiently represented using mixed sites, i.e. including scattering contributions from several elements in a site corresponding to a partial occupancy of the site by these elements, this method forming a very efficient basis for analyzing EXAFS data.en_US
dc.language.isoengen_US
dc.publisherRoyal Society of Chemistryen_US
dc.titleStrategies for the analysis of the elemental metal fraction of Ir and Ru oxides via XRD, XANES, and EXAFSen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionacceptedVersionen_US
dc.source.pagenumber12217-12230en_US
dc.source.volume21en_US
dc.source.journalPhysical Chemistry, Chemical Physics - PCCPen_US
dc.identifier.doi10.1039/C9CP01758E
dc.identifier.cristin1769861
dc.description.localcode© 2019. This is the authors' accepted and refereed manuscript to the article. The final authenticated version is available online at: http://dx.doi.org/10.1039/C9CP01758Een_US
cristin.unitcode194,66,35,0
cristin.unitcode194,66,25,0
cristin.unitnameInstitutt for materialteknologi
cristin.unitnameInstitutt for kjemi
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.fulltextoriginal
cristin.qualitycode2


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