Publication:
Different reactivity of the various platinum oxides and chemisorbed oxygen in co oxidation on pt(111)

dc.contributor.coauthorMiller, Daniel
dc.contributor.coauthorCasalongue, Hernan Sanchez
dc.contributor.coauthorBluhm, Hendrik
dc.contributor.coauthorOgasawara, Hirohito
dc.contributor.coauthorNilsson, Anders
dc.contributor.departmentDepartment of Chemistry
dc.contributor.facultymemberYes
dc.contributor.kuauthorKaya, Sarp
dc.contributor.schoolcollegeinstituteCollege of Sciences
dc.date.accessioned2024-11-09T23:03:00Z
dc.date.issued2014
dc.description.abstractWe have used X-ray photoelectron spectroscopy and polarization-resolved 0 K-edge X-ray absorption spectroscopy to investigate the reactivity of various oxygen covered Pt(111) surfaces, which emerge under high temperature and pressure conditions, toward CO. We find that the reactivity of the O/Pt(111) system decreases monotonically with increasing oxygen coverage. of the three surface oxygen phases, viz., chemisorbed oxygen (O-ad), a PtO-like surface oxide, and alpha-PtO2 trilayers, O-ad exhibits the highest reactivity toward CO, whereas alpha-PtO2 trilayers exhibit the lowest. Pt(111) surfaces fully terminated by alpha-PtO2 trilayers are inert to CO. Here it is proposed that the reactive phase is either O-ad or PtO-like surface oxide phase on bare non-CO poisoned Pt regions with PtO2 as majority spectator species.
dc.description.fulltextNo
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessNO
dc.description.peerreviewstatusN/A
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipU.S. Department of Energy (DOE), Basic Energy Science (BES) through the SUNCAT Center for Interface Science and Catalysis [DE-AC02-76SF00515]
dc.description.sponsorshipStanford Synchrotron Radiation Laboratory
dc.description.sponsorshipUnited States Department of Energy (DOE) [DE-AC02-05CH11231]
dc.description.versionN/A
dc.identifier.doi10.1021/ja413125q
dc.identifier.eissn1520-5126
dc.identifier.embargoN/A
dc.identifier.endpage6347
dc.identifier.grantnoDE-AC02-76SF00515
dc.identifier.grantnoDE-AC02-05CH11231
dc.identifier.issn0002-7863
dc.identifier.issue17
dc.identifier.pubmed24708067
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-84899707567
dc.identifier.startpage6340
dc.identifier.urihttps://doi.org/10.1021/ja413125q
dc.identifier.urihttps://hdl.handle.net/20.500.14288/8378
dc.identifier.volume136
dc.identifier.wos000335369200037
dc.keywordsChemisorption
dc.keywordsOxygen
dc.keywordsPhotoelectrons
dc.keywords X ray absorption spectroscopy
dc.keywordsX ray photoelectron spectroscopy
dc.language.isoeng
dc.publisherAmerican Chemical Society
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofJournal of the American Chemical Society
dc.relation.openaccessN/A
dc.rightsN/A
dc.subjectChemistry
dc.titleDifferent reactivity of the various platinum oxides and chemisorbed oxygen in co oxidation on pt(111)
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorKaya, Sarp
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