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dc.contributor.author
Henning, Sebastian
dc.contributor.author
Shimizu, Ryo
dc.contributor.author
Herranz, Juan
dc.contributor.author
Kuehn, Laura
dc.contributor.author
Eychmueller, Alexander
dc.contributor.author
Uchida, Makoto
dc.contributor.author
Kakinuma, Katsuyoshi
dc.contributor.author
Schmidt, Thomas
dc.date.accessioned
2018-05-22T11:41:59Z
dc.date.available
2018-05-18T17:04:25Z
dc.date.available
2018-05-22T11:41:59Z
dc.date.issued
2018-01-06
dc.identifier.issn
0013-4651
dc.identifier.issn
1945-7111
dc.identifier.other
10.1149/2.0531802jes
en_US
dc.identifier.uri
http://hdl.handle.net/20.500.11850/265148
dc.identifier.doi
10.3929/ethz-b-000265148
dc.description.abstract
Mitigating catalyst corrosion is crucial for the commercial success of polymer electrolyte fuel cells (PEFCs). Novel catalysts that can withstand the harsh conditions in case of gross fuel (i.e. H2) starvation events at the PEFC anode are needed to increase the fuel cell stack's service life and to meet the durability targets set for automotive applications. To make progress in this respect, we have tested an unsupported, bimetallic Pt3Ni alloy (aerogel) catalyst at the PEFC anode and subjected it to a stress test that mimics the high potentials (≥ 1.5 V vs. the reversible hydrogen electrode) encountered upon fuel starvation. In contrast to commercial carbon-supported platinum catalysts (Pt/C), the Pt3Ni aerogel displays excellent durability and performance retention in end-of-life fuel cell polarization curves. Additionally, the aerogel catalyst shows ≈35% higher surface-specific activity for the hydrogen oxidation/evolution reaction than Pt/C. These results highlight the great potential of using novel unsupported catalysts at the anode of PEFCs.
en_US
dc.format
application/pdf
en_US
dc.language.iso
en
en_US
dc.publisher
The Electrochemical Society
en_US
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.title
Unsupported Pt3Ni Aerogels as Corrosion Resistant PEFC Anode Catalysts under Gross Fuel Starvation Conditions
en_US
dc.type
Journal Article
dc.rights.license
Creative Commons Attribution 4.0 International
ethz.journal.title
Journal of the Electrochemical Society
ethz.journal.volume
165
en_US
ethz.journal.issue
6
en_US
ethz.journal.abbreviated
J. Electrochem. Soc.
ethz.pages.start
F3001
en_US
ethz.pages.end
F3006
en_US
ethz.version.deposit
publishedVersion
en_US
ethz.identifier.wos
ethz.publication.place
Pennington, NJ
ethz.publication.status
published
en_US
ethz.leitzahl
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02020 - Dep. Chemie und Angewandte Biowiss. / Dep. of Chemistry and Applied Biosc.::02543 - Inst. f. Molekulare Physikalische Wiss. / Institute of Molecular Physical Science::03910 - Schmidt, Thomas J. / Schmidt, Thomas J.
ethz.leitzahl.certified
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02020 - Dep. Chemie und Angewandte Biowiss. / Dep. of Chemistry and Applied Biosc.::02543 - Inst. f. Molekulare Physikalische Wiss. / Institute of Molecular Physical Science::03910 - Schmidt, Thomas J. / Schmidt, Thomas J.
ethz.date.deposited
2018-05-18T17:04:26Z
ethz.source
WOS
ethz.eth
yes
en_US
ethz.availability
Open access
en_US
ethz.rosetta.installDate
2018-05-22T11:42:05Z
ethz.rosetta.lastUpdated
2024-02-02T04:51:21Z
ethz.rosetta.versionExported
true
ethz.COinS
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