The rate of anion and hydrogen adsorption on Pt(111) and Rh(111)
Impedance spectra were measured for Pt(111) and Rh(111) electrodes in various electrolytes. They can all be interpreted by assuming one or two parallel adsorption resistances in addition to the double layer capacity. Adsorption of Cl − and HSO 4 − at Pt(111) is very fast and at the limit of detectab...
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Veröffentlicht in: | Electrochimica acta 1998-11, Vol.44 (6), p.909-918 |
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creator | Langkau, T. Baltruschat, H. |
description | Impedance spectra were measured for Pt(111) and Rh(111) electrodes in various electrolytes. They can all be interpreted by assuming one or two parallel adsorption resistances in addition to the double layer capacity. Adsorption of Cl
− and HSO
4
− at Pt(111) is very fast and at the limit of detectability. Adsorption of H
2PO
4
− has to be described by two parallel adsorption reactions, one of which is possibly an adsorption connected with deprotonation. Adsorption of hydrogen at Rh(111) is much slower than at Pt(111); surface roughness has opposing effects on both metals and leads to an increased adsorption rate at Rh. |
doi_str_mv | 10.1016/S0013-4686(98)00194-7 |
format | Article |
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− and HSO
4
− at Pt(111) is very fast and at the limit of detectability. Adsorption of H
2PO
4
− has to be described by two parallel adsorption reactions, one of which is possibly an adsorption connected with deprotonation. Adsorption of hydrogen at Rh(111) is much slower than at Pt(111); surface roughness has opposing effects on both metals and leads to an increased adsorption rate at Rh.</description><identifier>ISSN: 0013-4686</identifier><identifier>EISSN: 1873-3859</identifier><identifier>DOI: 10.1016/S0013-4686(98)00194-7</identifier><identifier>CODEN: ELCAAV</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Adsorption ; Chemistry ; Electrochemistry ; Exact sciences and technology ; General and physical chemistry ; Study of interfaces</subject><ispartof>Electrochimica acta, 1998-11, Vol.44 (6), p.909-918</ispartof><rights>1998 Elsevier Science Ltd</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c433t-c451c16ee5ff4fec0e0c3ddf1f771e2fc23aa5102b3dfbfe270a80d67db80cf53</citedby><cites>FETCH-LOGICAL-c433t-c451c16ee5ff4fec0e0c3ddf1f771e2fc23aa5102b3dfbfe270a80d67db80cf53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0013-4686(98)00194-7$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>309,310,314,780,784,789,790,3541,23921,23922,25131,27915,27916,45986</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1670042$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Langkau, T.</creatorcontrib><creatorcontrib>Baltruschat, H.</creatorcontrib><title>The rate of anion and hydrogen adsorption on Pt(111) and Rh(111)</title><title>Electrochimica acta</title><description>Impedance spectra were measured for Pt(111) and Rh(111) electrodes in various electrolytes. They can all be interpreted by assuming one or two parallel adsorption resistances in addition to the double layer capacity. Adsorption of Cl
− and HSO
4
− at Pt(111) is very fast and at the limit of detectability. Adsorption of H
2PO
4
− has to be described by two parallel adsorption reactions, one of which is possibly an adsorption connected with deprotonation. Adsorption of hydrogen at Rh(111) is much slower than at Pt(111); surface roughness has opposing effects on both metals and leads to an increased adsorption rate at Rh.</description><subject>Adsorption</subject><subject>Chemistry</subject><subject>Electrochemistry</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Study of interfaces</subject><issn>0013-4686</issn><issn>1873-3859</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNqFkN9LwzAQgIMoOKd_gtAHEfdQvTRtkz6pDH_BQNH5HLLk4iJdO5NO2H9v1g19FMIld3yX4z5CTilcUqDl1RsAZWleivKiEqOYVHnK98iACs5SJopqnwx-kUNyFMInAPCSw4DcTOeYeNVh0tpENa5tYjTJfG18-4ExMaH1y25Tj-elu6CUjnrkdd6_j8mBVXXAk909JO_3d9PxYzp5fnga305SnTPWxVhQTUvEwtrcogYEzYyx1HJOMbM6Y0oVFLIZM3ZmMeOgBJiSm5kAbQs2JOfbf5e-_Vph6OTCBY11rRpsV0FmJc9BUBHBYgtq34bg0cqldwvl15KC3PiSvS-5kSErIXtfkse-s90AFbSqrVeNduGvOeqCPIvY9RbDuOy3Qy-DdthoNM6j7qRp3T-DfgDscnz3</recordid><startdate>19981101</startdate><enddate>19981101</enddate><creator>Langkau, T.</creator><creator>Baltruschat, H.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>19981101</creationdate><title>The rate of anion and hydrogen adsorption on Pt(111) and Rh(111)</title><author>Langkau, T. ; Baltruschat, H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c433t-c451c16ee5ff4fec0e0c3ddf1f771e2fc23aa5102b3dfbfe270a80d67db80cf53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Adsorption</topic><topic>Chemistry</topic><topic>Electrochemistry</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Study of interfaces</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Langkau, T.</creatorcontrib><creatorcontrib>Baltruschat, H.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Electronics & Communications Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Electrochimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Langkau, T.</au><au>Baltruschat, H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The rate of anion and hydrogen adsorption on Pt(111) and Rh(111)</atitle><jtitle>Electrochimica acta</jtitle><date>1998-11-01</date><risdate>1998</risdate><volume>44</volume><issue>6</issue><spage>909</spage><epage>918</epage><pages>909-918</pages><issn>0013-4686</issn><eissn>1873-3859</eissn><coden>ELCAAV</coden><abstract>Impedance spectra were measured for Pt(111) and Rh(111) electrodes in various electrolytes. They can all be interpreted by assuming one or two parallel adsorption resistances in addition to the double layer capacity. Adsorption of Cl
− and HSO
4
− at Pt(111) is very fast and at the limit of detectability. Adsorption of H
2PO
4
− has to be described by two parallel adsorption reactions, one of which is possibly an adsorption connected with deprotonation. Adsorption of hydrogen at Rh(111) is much slower than at Pt(111); surface roughness has opposing effects on both metals and leads to an increased adsorption rate at Rh.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/S0013-4686(98)00194-7</doi><tpages>10</tpages></addata></record> |
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source | Elsevier ScienceDirect Journals Complete - AutoHoldings |
subjects | Adsorption Chemistry Electrochemistry Exact sciences and technology General and physical chemistry Study of interfaces |
title | The rate of anion and hydrogen adsorption on Pt(111) and Rh(111) |
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