Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.elecom.2007.03.016
DC FieldValue
dc.titleHighly active core-shell Au@Pd catalyst for formic acid electrooxidation
dc.contributor.authorZhou, W.
dc.contributor.authorLee, J.Y.
dc.date.accessioned2014-06-17T07:42:18Z
dc.date.available2014-06-17T07:42:18Z
dc.date.issued2007-07
dc.identifier.citationZhou, W., Lee, J.Y. (2007-07). Highly active core-shell Au@Pd catalyst for formic acid electrooxidation. Electrochemistry Communications 9 (7) : 1725-1729. ScholarBank@NUS Repository. https://doi.org/10.1016/j.elecom.2007.03.016
dc.identifier.issn13882481
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/64020
dc.description.abstractCarbon supported bimetallic Au-Pd catalysts with the core-shell structure were prepared by the successive reduction method. TEM, XRD, XPS and UV-vis spectrum were used to characterize the core-shell sample and the monometallic samples. The electrochemical tests (cyclic voltammetry (CV) and chronoamperometry (CA)) showed that the core-shell structure could significantly improve the catalytic activity and stability of Pd in the room temperature electrooxidation of formic acid. The carbon supported pure Au sample showed no activity to the electrooxidation of formic acid and CO. The improvement of activity is ascribed to the interaction between Pd shell and Au core. © 2007 Elsevier B.V. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.elecom.2007.03.016
dc.sourceScopus
dc.subjectCore-shell
dc.subjectFormic acid electrooxidation
dc.subjectGold
dc.subjectPalladium
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1016/j.elecom.2007.03.016
dc.description.sourcetitleElectrochemistry Communications
dc.description.volume9
dc.description.issue7
dc.description.page1725-1729
dc.description.codenECCMF
dc.identifier.isiut000248089400057
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