dc.contributor.author | Strømsheim, Marie Døvre | |
dc.contributor.author | Knudsen, Jan | |
dc.contributor.author | Farstad, Mari Helene | |
dc.contributor.author | Sørvik, Linn Cecilie | |
dc.contributor.author | Guo, Xiaoyang | |
dc.contributor.author | Venvik, Hilde Johnsen | |
dc.contributor.author | Borg, Anne | |
dc.date.accessioned | 2017-12-21T08:07:13Z | |
dc.date.available | 2017-12-21T08:07:13Z | |
dc.date.created | 2017-12-20T10:37:58Z | |
dc.date.issued | 2017 | |
dc.identifier.citation | Topics in catalysis. 2017, 60 (17-18), 1439-1448. | nb_NO |
dc.identifier.issn | 1022-5528 | |
dc.identifier.uri | http://hdl.handle.net/11250/2473377 | |
dc.description.abstract | The CO oxidation behavior under excess oxygen and near stoichiometric conditions over the surface of Pd3Au(100) has been studied by combining near-ambient pressure X-ray photoelectron spectroscopy and quadrupole mass spectrometry and compared to Pd(100). During heating and cooling cycles, normal hysteresis in the CO2 production, i.e. with the light-off temperature being higher than the extinction temperature, is observed for both surfaces. On both Pd3Au(100) and Pd(100) the (√5 × √5)R27° surface oxide structure is present during CO2 production under excess oxygen conditions (O2:CO = 10:1), while at near stoichiometric conditions (O2:CO = 1:1) the surfaces are covered with atomic oxygen. Au as alloying element hence induces only minor differences in the observed hysteresis and the active phase compared to pure Pd. Alloying with Au thus yields a different behavior compared to Ag, where reversed hysteresis is observed for CO2 production over Pd75Ag25(100) at similar conditions [Fernandes et al., ACS Catal. (2016) 4154]. | nb_NO |
dc.language.iso | eng | nb_NO |
dc.publisher | Springer Verlag | nb_NO |
dc.title | Near Ambient Pressure XPS Investigation of CO Oxidation Over Pd3Au(100) | nb_NO |
dc.type | Journal article | nb_NO |
dc.type | Peer reviewed | nb_NO |
dc.description.version | acceptedVersion | nb_NO |
dc.source.pagenumber | 1439-1448 | nb_NO |
dc.source.volume | 60 | nb_NO |
dc.source.journal | Topics in catalysis | nb_NO |
dc.source.issue | 17-18 | nb_NO |
dc.identifier.doi | 10.1007/s11244-017-0831-z | |
dc.identifier.cristin | 1530211 | |
dc.relation.project | Norges forskningsråd: 174893 | nb_NO |
dc.relation.project | Vetenskapsrådet: 2012–3850 | nb_NO |
dc.relation.project | Nordforsk: 40521 | nb_NO |
dc.description.localcode | This is a post-peer-review, pre-copyedit version of an article published in Topics in Catalysis . The final authenticated version is available online at: http://dx.doi.org/10.1007/s11244-017-0831-z | nb_NO |
cristin.unitcode | 194,66,30,0 | |
cristin.unitcode | 194,14,0,0 | |
cristin.unitname | Institutt for kjemisk prosessteknologi | |
cristin.unitname | Prorektor for utdanning | |
cristin.ispublished | true | |
cristin.fulltext | postprint | |
cristin.qualitycode | 1 | |