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dc.contributor.authorHuang, CAen_US
dc.contributor.authorLi, KCen_US
dc.contributor.authorTu, GCen_US
dc.contributor.authorWang, WSen_US
dc.date.accessioned2014-12-08T15:40:11Z-
dc.date.available2014-12-08T15:40:11Z-
dc.date.issued2003-10-30en_US
dc.identifier.issn0013-4686en_US
dc.identifier.urihttp://dx.doi.org/10.1016/S0013-4686(03)00480-8en_US
dc.identifier.urihttp://hdl.handle.net/11536/27446-
dc.description.abstractThe electrochemical behavior of tin-doped indium oxide (ITO) on SiO2 in 0.3 M HCl was studied using voltammetric scanning method. The result showed that an obvious reduction current peak occurred during the first cathodic potential scanning. The reduction reaction became less active after annealing ITO at 500 C for 1 h. The result was attributed to the replenishment of oxygen-deficient site, which acts as current carrier, by the annealing treatment. Many spherical In-Sn particles with sizes about 100-500 nm were formed on the ITO surface adjacent to the grain boundary when the reduction current took place. The In-Sn particles initiated preferentially on the ITO surface near grain boundaries attending the dissolution of ITO grain boundary. In the scanning period, after completion of the reduction current peak, reduction of hydrogen ions occurred in more negative potential region. A schematic illustration for the formation mechanism of the In-Sn reduction particle was postulated based on the metallographical and electrochemical results in this work. (C) 2003 Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjecttin-doped indium oxideen_US
dc.subjectvoltammetric scanningen_US
dc.subjectreduction producten_US
dc.subjectIn-Sn particleen_US
dc.subjectFESEMen_US
dc.subjectEDSen_US
dc.titleThe electrochemical behavior of tin-doped indium oxide during reduction in 0.3 M hydrochloric aciden_US
dc.typeArticleen_US
dc.identifier.doi10.1016/S0013-4686(03)00480-8en_US
dc.identifier.journalELECTROCHIMICA ACTAen_US
dc.citation.volume48en_US
dc.citation.issue24en_US
dc.citation.spage3599en_US
dc.citation.epage3605en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000185674600003-
dc.citation.woscount20-
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