Selective dissolution of binary Pt–Co alloys of different compositions in sulphuric acid solution
► The Pt-enriched layer is formed on the surface of the Pt–Co alloys due to selective dissolution of Co. ► The selective dissolution of Co from Pt30–Co70 increases linearly with time. ► The selective dissolution of Co from Pt–Co alloys is enhanced by potential cycling. ► The amount of dissolved ions...
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| Veröffentlicht in: | Corrosion science 2012-12, Vol.65, p.512-519 |
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| creator | Hoshi, Yoshinao Ozawa, Ryo Tada, Eiji Nishikata, Atsushi Tsuru, Tooru |
| description | ► The Pt-enriched layer is formed on the surface of the Pt–Co alloys due to selective dissolution of Co. ► The selective dissolution of Co from Pt30–Co70 increases linearly with time. ► The selective dissolution of Co from Pt–Co alloys is enhanced by potential cycling. ► The amount of dissolved ions from Pt–Co alloys was determined with ICP-MS.
The dissolution of Pt–Co alloys in a 0.5M H2SO4 solution has been studied under immersion and potential cycling conditions. Under immersion conditions, the Pt-enriched layer formed on Pt50–Co50 and Pt40–Co60 alloys suppresses further dissolution of Co. Potential cycling between 0 and 1.4V vs. standard hydrogen electrode enhances the selective dissolution, but is suppressed in the initial stage. In contrast, the amount of selective dissolution of Co from Pt30–Co70 increases linearly with time during the immersion. Potential cycling significantly accelerates the selective dissolution of Pt30–Co70. The selective dissolution mechanism of Pt–Co alloys is discussed in this paper. |
| doi_str_mv | 10.1016/j.corsci.2012.08.058 |
| format | Article |
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The dissolution of Pt–Co alloys in a 0.5M H2SO4 solution has been studied under immersion and potential cycling conditions. Under immersion conditions, the Pt-enriched layer formed on Pt50–Co50 and Pt40–Co60 alloys suppresses further dissolution of Co. Potential cycling between 0 and 1.4V vs. standard hydrogen electrode enhances the selective dissolution, but is suppressed in the initial stage. In contrast, the amount of selective dissolution of Co from Pt30–Co70 increases linearly with time during the immersion. Potential cycling significantly accelerates the selective dissolution of Pt30–Co70. The selective dissolution mechanism of Pt–Co alloys is discussed in this paper.</description><identifier>ISSN: 0010-938X</identifier><identifier>EISSN: 1879-0496</identifier><identifier>DOI: 10.1016/j.corsci.2012.08.058</identifier><identifier>CODEN: CRRSAA</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>A. Alloy ; A. fuel cell ; A. Platinum ; Alloys ; Applied sciences ; B. Cyclic voltammetry ; B. ICP-OES ; C. anodic dissolution ; Corrosion ; Corrosion environments ; Cycles ; Dissolution ; Electrodes ; Exact sciences and technology ; Immersion ; Metals. Metallurgy ; Platinum base alloys</subject><ispartof>Corrosion science, 2012-12, Vol.65, p.512-519</ispartof><rights>2012 Elsevier Ltd</rights><rights>2014 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c476t-e474487bb0dd03705fb999d58f70d8becc9c54f3619bbda03d5023bcdc05db4e3</citedby><cites>FETCH-LOGICAL-c476t-e474487bb0dd03705fb999d58f70d8becc9c54f3619bbda03d5023bcdc05db4e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.corsci.2012.08.058$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26496513$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Hoshi, Yoshinao</creatorcontrib><creatorcontrib>Ozawa, Ryo</creatorcontrib><creatorcontrib>Tada, Eiji</creatorcontrib><creatorcontrib>Nishikata, Atsushi</creatorcontrib><creatorcontrib>Tsuru, Tooru</creatorcontrib><title>Selective dissolution of binary Pt–Co alloys of different compositions in sulphuric acid solution</title><title>Corrosion science</title><description>► The Pt-enriched layer is formed on the surface of the Pt–Co alloys due to selective dissolution of Co. ► The selective dissolution of Co from Pt30–Co70 increases linearly with time. ► The selective dissolution of Co from Pt–Co alloys is enhanced by potential cycling. ► The amount of dissolved ions from Pt–Co alloys was determined with ICP-MS.
The dissolution of Pt–Co alloys in a 0.5M H2SO4 solution has been studied under immersion and potential cycling conditions. Under immersion conditions, the Pt-enriched layer formed on Pt50–Co50 and Pt40–Co60 alloys suppresses further dissolution of Co. Potential cycling between 0 and 1.4V vs. standard hydrogen electrode enhances the selective dissolution, but is suppressed in the initial stage. In contrast, the amount of selective dissolution of Co from Pt30–Co70 increases linearly with time during the immersion. Potential cycling significantly accelerates the selective dissolution of Pt30–Co70. The selective dissolution mechanism of Pt–Co alloys is discussed in this paper.</description><subject>A. Alloy</subject><subject>A. fuel cell</subject><subject>A. Platinum</subject><subject>Alloys</subject><subject>Applied sciences</subject><subject>B. Cyclic voltammetry</subject><subject>B. ICP-OES</subject><subject>C. anodic dissolution</subject><subject>Corrosion</subject><subject>Corrosion environments</subject><subject>Cycles</subject><subject>Dissolution</subject><subject>Electrodes</subject><subject>Exact sciences and technology</subject><subject>Immersion</subject><subject>Metals. Metallurgy</subject><subject>Platinum base alloys</subject><issn>0010-938X</issn><issn>1879-0496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNp9kMFqFTEUhoMoeK2-gYtsCm5mPJnJzCSbglxaFQoKKnQXkpOE5pI7uU1mCt35Dr6hT9Jcbu3S1Vmc7_8P5yPkPYOWARs_7lpMuWBoO2BdC6KFQbwgGyYm2QCX40uyAWDQyF7cvCZvStkBQGVhQ_CHiw6XcO-oDaWkuC4hzTR5asKs8wP9vvz9_WebqI4xPZTjwgbvXXbzQjHtD6mEY6LQMNOyxsPtmgNSjcHSf21vySuvY3HvnuYZ-XV1-XP7pbn-9vnr9tN1g3wal8bxiXMxGQPWQj_B4I2U0g7CT2CFcYgSB-77kUljrIbeDtD1Bi3CYA13_Rn5cOo95HS3urKofSjoYtSzS2tRjI98EF0vp4ryE4o5lZKdV4cc9vVfxUAdnaqdOjlVR6cKhKpOa-z86YIuqKPPesZQnrPdWGUPrK_cxYlz9d374LKqTW5GZ0OutpVN4f-HHgFYA5I2</recordid><startdate>20121201</startdate><enddate>20121201</enddate><creator>Hoshi, Yoshinao</creator><creator>Ozawa, Ryo</creator><creator>Tada, Eiji</creator><creator>Nishikata, Atsushi</creator><creator>Tsuru, Tooru</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SE</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>JG9</scope></search><sort><creationdate>20121201</creationdate><title>Selective dissolution of binary Pt–Co alloys of different compositions in sulphuric acid solution</title><author>Hoshi, Yoshinao ; Ozawa, Ryo ; Tada, Eiji ; Nishikata, Atsushi ; Tsuru, Tooru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c476t-e474487bb0dd03705fb999d58f70d8becc9c54f3619bbda03d5023bcdc05db4e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>A. Alloy</topic><topic>A. fuel cell</topic><topic>A. Platinum</topic><topic>Alloys</topic><topic>Applied sciences</topic><topic>B. Cyclic voltammetry</topic><topic>B. ICP-OES</topic><topic>C. anodic dissolution</topic><topic>Corrosion</topic><topic>Corrosion environments</topic><topic>Cycles</topic><topic>Dissolution</topic><topic>Electrodes</topic><topic>Exact sciences and technology</topic><topic>Immersion</topic><topic>Metals. Metallurgy</topic><topic>Platinum base alloys</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hoshi, Yoshinao</creatorcontrib><creatorcontrib>Ozawa, Ryo</creatorcontrib><creatorcontrib>Tada, Eiji</creatorcontrib><creatorcontrib>Nishikata, Atsushi</creatorcontrib><creatorcontrib>Tsuru, Tooru</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Corrosion Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><jtitle>Corrosion science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hoshi, Yoshinao</au><au>Ozawa, Ryo</au><au>Tada, Eiji</au><au>Nishikata, Atsushi</au><au>Tsuru, Tooru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Selective dissolution of binary Pt–Co alloys of different compositions in sulphuric acid solution</atitle><jtitle>Corrosion science</jtitle><date>2012-12-01</date><risdate>2012</risdate><volume>65</volume><spage>512</spage><epage>519</epage><pages>512-519</pages><issn>0010-938X</issn><eissn>1879-0496</eissn><coden>CRRSAA</coden><abstract>► The Pt-enriched layer is formed on the surface of the Pt–Co alloys due to selective dissolution of Co. ► The selective dissolution of Co from Pt30–Co70 increases linearly with time. ► The selective dissolution of Co from Pt–Co alloys is enhanced by potential cycling. ► The amount of dissolved ions from Pt–Co alloys was determined with ICP-MS.
The dissolution of Pt–Co alloys in a 0.5M H2SO4 solution has been studied under immersion and potential cycling conditions. Under immersion conditions, the Pt-enriched layer formed on Pt50–Co50 and Pt40–Co60 alloys suppresses further dissolution of Co. Potential cycling between 0 and 1.4V vs. standard hydrogen electrode enhances the selective dissolution, but is suppressed in the initial stage. In contrast, the amount of selective dissolution of Co from Pt30–Co70 increases linearly with time during the immersion. Potential cycling significantly accelerates the selective dissolution of Pt30–Co70. The selective dissolution mechanism of Pt–Co alloys is discussed in this paper.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.corsci.2012.08.058</doi><tpages>8</tpages></addata></record> |
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| ispartof | Corrosion science, 2012-12, Vol.65, p.512-519 |
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| subjects | A. Alloy A. fuel cell A. Platinum Alloys Applied sciences B. Cyclic voltammetry B. ICP-OES C. anodic dissolution Corrosion Corrosion environments Cycles Dissolution Electrodes Exact sciences and technology Immersion Metals. Metallurgy Platinum base alloys |
| title | Selective dissolution of binary Pt–Co alloys of different compositions in sulphuric acid solution |
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