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dc.contributor.authorYan, Bing
dc.contributor.authorConcannon, Nolan M.
dc.contributor.authorMilshtein, Jarrod David
dc.contributor.authorBrushett, Fikile R
dc.contributor.authorSurendranath, Yogesh
dc.date.accessioned2018-04-30T19:32:47Z
dc.date.available2018-04-30T19:32:47Z
dc.date.issued2017-05
dc.identifier.issn1433-7851
dc.identifier.issn1521-3773
dc.identifier.urihttp://hdl.handle.net/1721.1/115115
dc.description.abstractPolymer electrolyte membranes employed in contemporary fuel cells severely limit device design and restrict catalyst choice, but are essential for preventing short‐circuiting reactions at unselective anode and cathode catalysts. Herein, we report that nickel sulfide Ni[subscript 3]S[subscript 2] is a highly selective catalyst for the oxygen reduction reaction in the presence of 1.0 m formate. We combine this selective cathode with a carbon‐supported palladium (Pd/C) anode to establish a membrane‐free, room‐temperature formate fuel cell that operates under benign neutral pH conditions. Proof‐of‐concept cells display open circuit voltages of approximately 0.7 V and peak power values greater than 1 mW cm[superscript −2], significantly outperforming the identical device employing an unselective platinum (Pt) cathode. The work establishes the power of selective catalysis to enable versatile membrane‐free fuel cells.en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (Award CHE-­1454060)en_US
dc.language.isoen_US
dc.publisherWiley Blackwellen_US
dc.relation.isversionofhttp://dx.doi.org/10.1002/anie.201702578en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourceProf. Surendranath via Erja Kajosaloen_US
dc.titleA Membrane-Free Neutral pH Formate Fuel Cell Enabled by a Selective Nickel Sulfide Oxygen Reduction Catalysten_US
dc.typeArticleen_US
dc.identifier.citationYan, Bing et al. “A Membrane-Free Neutral pH Formate Fuel Cell Enabled by a Selective Nickel Sulfide Oxygen Reduction Catalyst.” Angewandte Chemie International Edition 56, 26 (May 2017): 7496–7499 © 2017 Wiley Blackwellen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineeringen_US
dc.contributor.approverSurendranath, Yogeshen_US
dc.contributor.mitauthorYan, Bing
dc.contributor.mitauthorConcannon, Nolan M.
dc.contributor.mitauthorMilshtein, Jarrod David
dc.contributor.mitauthorBrushett, Fikile R
dc.contributor.mitauthorSurendranath, Yogesh
dc.relation.journalAngewandte Chemie International Editionen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsYan, Bing; Concannon, Nolan M.; Milshtein, Jarrod D.; Brushett, Fikile R.; Surendranath, Yogeshen_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0001-7874-725X
dc.identifier.orcidhttps://orcid.org/0000-0001-8322-5106
dc.identifier.orcidhttps://orcid.org/0000-0002-7361-6637
dc.identifier.orcidhttps://orcid.org/0000-0003-1016-3420
mit.licenseOPEN_ACCESS_POLICYen_US


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