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dc.contributor.authorGöhl, Daniel
dc.contributor.authorRueß, Holger
dc.contributor.authorSchlicht, Stefanie
dc.contributor.authorVogel, Alexandra
dc.contributor.authorRohwerder, Michael
dc.contributor.authorMayrhofer, Karl JJ
dc.contributor.authorBachmann, Julien
dc.contributor.authorRomán-Leshkov, Yuriy
dc.contributor.authorSchneider, Jochen M
dc.contributor.authorLedendecker, Marc
dc.date.accessioned2021-10-27T19:58:01Z
dc.date.available2021-10-27T19:58:01Z
dc.date.issued2020
dc.identifier.urihttps://hdl.handle.net/1721.1/134087
dc.description.abstract© 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. The development of stable, cost-efficient and active materials is one of the main challenges in catalysis. The utilization of platinum in the electroreduction of oxygen is a salient example where the development of new material combinations has led to a drastic increase in specific activity compared to bare platinum. These material classes comprise nanostructured thin films, platinum alloys, shape-controlled nanostructures and core–shell architectures. Excessive platinum substitution, however, leads to structural and catalytic instabilities. Herein, we introduce a catalyst concept that comprises the use of an atomically thin platinum film deposited on a potential-triggered passivating support. The model catalyst exhibits an equal specific activity with higher atom utilization compared to bulk platinum. By using potential-triggered passivation of titanium carbide, irregularities in the Pt film heal out via the formation of insoluble oxide species at the solid/liquid interface. The adaptation of the described catalyst design to the nanoscale and to high-surface-area structures highlight the potential for stable, passivating catalyst systems for various electrocatalytic reactions such as the oxygen reduction reaction.
dc.language.isoen
dc.publisherWiley
dc.relation.isversionof10.1002/CELC.202000278
dc.rightsCreative Commons Attribution 4.0 International license
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceWiley
dc.titleStable and Active Oxygen Reduction Catalysts with Reduced Noble Metal Loadings through Potential Triggered Support Passivation
dc.typeArticle
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineering
dc.relation.journalChemElectroChem
dc.eprint.versionFinal published version
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2021-06-22T17:00:16Z
dspace.orderedauthorsGöhl, D; Rueß, H; Schlicht, S; Vogel, A; Rohwerder, M; Mayrhofer, KJJ; Bachmann, J; Román-Leshkov, Y; Schneider, JM; Ledendecker, M
dspace.date.submission2021-06-22T17:00:17Z
mit.journal.volume7
mit.journal.issue11
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Needed


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