Highly Durable Platinum Single-Atom Alloy Catalyst for Electrochemical Reactions

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dc.contributor.authorKim, Jiwhanko
dc.contributor.authorRoh, Chi-Wooko
dc.contributor.authorSahoo, Suman Kalyanko
dc.contributor.authorYang, Sungeunko
dc.contributor.authorBae, Juneminko
dc.contributor.authorHan, Jeong Wooko
dc.contributor.authorLee, Hyunjooko
dc.date.accessioned2018-01-30T05:48:41Z-
dc.date.available2018-01-30T05:48:41Z-
dc.date.created2018-01-15-
dc.date.created2018-01-15-
dc.date.created2018-01-15-
dc.date.issued2018-01-
dc.identifier.citationADVANCED ENERGY MATERIALS, v.8, no.1, pp.1701476-
dc.identifier.issn1614-6832-
dc.identifier.urihttp://hdl.handle.net/10203/239452-
dc.description.abstractSingle atomic Pt catalyst can offer efficient utilization of the expensive platinum and provide unique selectivity because it lacks ensemble sites. However, designing such a catalyst with high Pt loading and good durability is very challenging. Here, single atomic Pt catalyst supported on antimony-doped tin oxide (Pt1/ATO) is synthesized by conventional incipient wetness impregnation, with up to 8 wt% Pt. The single atomic Pt structure is confirmed by high-angle annular dark field scanning tunneling electron microscopy images and extended X-ray absorption fine structure analysis results. Density functional theory calculations show that replacing Sb sites with Pt atoms in the bulk phase or at the surface of SbSn or ATO is energetically favorable. The Pt1/ATO shows superior activity and durability for formic acid oxidation reaction, compared to a commercial Pt/C catalyst. The single atomic Pt structure is retained even after a harsh durability test, which is performed by repeating cyclic voltammetry in the range of 0.05-1.4 V for 1800 cycles. A full cell is fabricated for direct formic acid fuel cell using the Pt1/ATO as an anode catalyst, and an order of magnitude higher cell power is obtained compared to the Pt/C.-
dc.languageEnglish-
dc.publisherWILEY-VCH VERLAG GMBH-
dc.subjectFORMIC-ACID OXIDATION-
dc.subjectATOMICALLY DISPERSED PLATINUM-
dc.subjectWATER-GAS SHIFT-
dc.subjectSELECTIVE HYDROGENATION-
dc.subjectOXYGEN REDUCTION-
dc.subjectCO OXIDATION-
dc.subjectFUEL-CELLS-
dc.subjectELECTROCATALYTIC OXIDATION-
dc.subjectABSORPTION SPECTROSCOPY-
dc.subjectCARBON-MONOXIDE-
dc.titleHighly Durable Platinum Single-Atom Alloy Catalyst for Electrochemical Reactions-
dc.typeArticle-
dc.identifier.wosid000419327200010-
dc.identifier.scopusid2-s2.0-85029051026-
dc.type.rimsART-
dc.citation.volume8-
dc.citation.issue1-
dc.citation.beginningpage1701476-
dc.citation.publicationnameADVANCED ENERGY MATERIALS-
dc.identifier.doi10.1002/aenm.201701476-
dc.contributor.localauthorLee, Hyunjoo-
dc.contributor.nonIdAuthorSahoo, Suman Kalyan-
dc.contributor.nonIdAuthorYang, Sungeun-
dc.contributor.nonIdAuthorHan, Jeong Woo-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorelectrocatalysts-
dc.subject.keywordAuthorformic acid oxidation-
dc.subject.keywordAuthorfuel cell-
dc.subject.keywordAuthorplatinum-
dc.subject.keywordAuthorsingle-atom alloy-
dc.subject.keywordPlusFORMIC-ACID OXIDATION-
dc.subject.keywordPlusATOMICALLY DISPERSED PLATINUM-
dc.subject.keywordPlusWATER-GAS SHIFT-
dc.subject.keywordPlusSELECTIVE HYDROGENATION-
dc.subject.keywordPlusOXYGEN REDUCTION-
dc.subject.keywordPlusCO OXIDATION-
dc.subject.keywordPlusFUEL-CELLS-
dc.subject.keywordPlusELECTROCATALYTIC OXIDATION-
dc.subject.keywordPlusABSORPTION SPECTROSCOPY-
dc.subject.keywordPlusCARBON-MONOXIDE-
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