Electro-Oxidation of Ni42 Steel: A Highly Active Bifunctional Electrocatalyst

DC ElementWertSprache
dc.contributor.authorSchaefer, Helmut
dc.contributor.authorChevrier, Daniel M.
dc.contributor.authorZhang, Peng
dc.contributor.authorStangl, Johannes
dc.contributor.authorMueller-Buschbaum, Klaus
dc.contributor.authorHardege, Jorg D.
dc.contributor.authorKuepper, Karsten
dc.contributor.authorWollschlaeger, Joachim
dc.contributor.authorKrupp, Ulrich
dc.contributor.authorDuehnen, Simon
dc.contributor.authorSteinhart, Martin
dc.contributor.authorWalder, Lorenz
dc.contributor.authorSadaf, Shamaila
dc.contributor.authorSchmidt, Mercedes
dc.date.accessioned2021-12-23T16:20:14Z-
dc.date.available2021-12-23T16:20:14Z-
dc.date.issued2016
dc.identifier.issn1616301X
dc.identifier.urihttps://osnascholar.ub.uni-osnabrueck.de/handle/unios/13375-
dc.description.abstractJanus type water-splitting catalysts have attracted highest attention as a tool of choice for solar to fuel conversion. AISI Ni42 steel is upon harsh anodization converted into a bifunctional electrocatalyst. Oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) are highly efficiently and steadfast catalyzed at pH 7, 13, 14, 14.6 (OER) and at pH 0, 1, 13, 14, 14.6 (HER), respectively. The current density taken from long-term OER measurements in pH 7 buffer solution upon the electro-activated steel at 491 mV overpotential (eta) is around four times higher (4 mA cm(-2)) in comparison with recently developed OER electrocatalysts. The very strong voltage-current behavior of the catalyst shown in OER polarization experiments at both pH 7 and at pH 13 are even superior to those known for IrO2 center dot RuO2. No degradation of the catalyst is detected even when conditions close to standard industrial operations are applied to the catalyst. A stable Ni-, Fe-oxide based passivating layer sufficiently protects the bare metal for further oxidation. Quantitative charge to oxygen (OER) and charge to hydrogen (HER) conversion are confirmed. High-resolution XPS spectra show that most likely gamma-NiO(OH) and FeO(OH) are the catalytic active OER and NiO is the catalytic active HER species.
dc.description.sponsorshipNSERC CGS-Alexander Graham Bell scholarship; NSERCNatural Sciences and Engineering Research Council of Canada (NSERC); European Research Council (ERC-CoG) [646742]; D.M.C. was supported by the NSERC CGS-Alexander Graham Bell scholarship and P.Z. acknowledges the NSERC Discovery Grant for funding. A special thank you is given to Andrew George (Dalhousie University, Department of Physics) for his technical assistance during XPS experiments. Mercedes Schmidt was supported by the European Research Council (ERC-CoG-2014; project 646742 INCANA).
dc.language.isoen
dc.publisherWILEY-V C H VERLAG GMBH
dc.relation.ispartofADVANCED FUNCTIONAL MATERIALS
dc.subjectChemistry
dc.subjectChemistry, Multidisciplinary
dc.subjectChemistry, Physical
dc.subjectELECTROCHEMICAL EVOLUTION
dc.subjectEVOLVING CATALYST
dc.subjectHYDROGEN EVOLUTION
dc.subjectIN-SITU
dc.subjectIRON ELECTRODES
dc.subjectMaterials Science
dc.subjectMaterials Science, Multidisciplinary
dc.subjectNanoscience & Nanotechnology
dc.subjectOXYGEN EVOLUTION REACTION
dc.subjectPhysics
dc.subjectPhysics, Applied
dc.subjectPhysics, Condensed Matter
dc.subjectRUTHENIUM DIOXIDE
dc.subjectScience & Technology - Other Topics
dc.subjectSTAINLESS-STEEL
dc.subjectTHIN-FILM
dc.subjectWATER-OXIDATION CATALYSTS
dc.titleElectro-Oxidation of Ni42 Steel: A Highly Active Bifunctional Electrocatalyst
dc.typejournal article
dc.identifier.doi10.1002/adfm.201601581
dc.identifier.isiISI:000384809100006
dc.description.volume26
dc.description.issue35
dc.description.startpage6402
dc.description.endpage6417
dc.contributor.orcid0000-0002-5241-8498
dc.contributor.orcid0000-0003-3603-0175
dc.contributor.orcid0000-0001-5906-3354
dc.contributor.orcid0000-0003-3603-0175
dc.contributor.orcid0000-0002-0914-6714
dc.contributor.orcid0000-0002-5497-034X
dc.contributor.researcheridB-7811-2011
dc.contributor.researcheridAAP-5787-2020
dc.contributor.researcheridD-7919-2011
dc.contributor.researcheridK-5174-2012
dc.contributor.researcheridAAI-7027-2021
dc.identifier.eissn16163028
dc.publisher.placePOSTFACH 101161, 69451 WEINHEIM, GERMANY
dcterms.isPartOf.abbreviationAdv. Funct. Mater.
dcterms.oaStatusGreen Submitted
crisitem.author.deptFB 04 - Physik-
crisitem.author.deptFB 04 - Physik-
crisitem.author.deptInstitut für Chemie neuer Materialien-
crisitem.author.deptidfb04-
crisitem.author.deptidfb04-
crisitem.author.deptidinstitute11-
crisitem.author.orcid0000-0002-3043-3718-
crisitem.author.orcid0000-0002-5241-8498-
crisitem.author.orcid0000-0002-5497-034X-
crisitem.author.parentorgUniversität Osnabrück-
crisitem.author.parentorgUniversität Osnabrück-
crisitem.author.parentorgFB 05 - Biologie/Chemie-
crisitem.author.grandparentorgUniversität Osnabrück-
crisitem.author.netidKuKa120-
crisitem.author.netidWoJo788-
crisitem.author.netidStMa946-
crisitem.author.netidWaLo966-
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