In situ determination of the surface excess upon electrochemical sulfate adsorption on Au(111) films by surface plasmon resonance
For the independent and simultaneous characterization of electrochemical processes, we employ surface plasmon resonance (SPR) detection together with standard electrochemical methods. As a first test system we studied sulfate adsorption on Au(111). After careful calibration of the SPR signal we obta...
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Veröffentlicht in: | Physical chemistry chemical physics : PCCP 2013-05, Vol.15 (18), p.6667-6672 |
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creator | Timm, Axel Eric Nattland, Detlef Schuster, Rolf |
description | For the independent and simultaneous characterization of electrochemical processes, we employ surface plasmon resonance (SPR) detection together with standard electrochemical methods. As a first test system we studied sulfate adsorption on Au(111). After careful calibration of the SPR signal we obtained submonolayer sensitivity on a millisecond time scale. The experimental data are simulated within the framework of a layer stack model of the optical interface. The sulfate adsorbate is simply described, employing the optical properties of sulfuric acid. The obtained potential dependent sulfate coverage is in reasonable agreement with independent results as presented in the literature.
We have studied sulfate adsorption and desorption processes on gold surfaces, employing time resolved surface plasmon generation. |
doi_str_mv | 10.1039/c3cp44303e |
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We have studied sulfate adsorption and desorption processes on gold surfaces, employing time resolved surface plasmon generation.</description><identifier>ISSN: 1463-9076</identifier><identifier>EISSN: 1463-9084</identifier><identifier>DOI: 10.1039/c3cp44303e</identifier><identifier>PMID: 23439972</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Adsorption ; Calibration ; Chemistry ; Electrochemistry ; Exact sciences and technology ; General and physical chemistry ; Mathematical models ; Optical properties ; Plasmons ; Sulfates ; Surface chemistry ; Surface physical chemistry</subject><ispartof>Physical chemistry chemical physics : PCCP, 2013-05, Vol.15 (18), p.6667-6672</ispartof><rights>2014 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c398t-a9143d34b6ac120ace1634a367496c25e59dfbb66c210eebe9fde6310760a5053</citedby><cites>FETCH-LOGICAL-c398t-a9143d34b6ac120ace1634a367496c25e59dfbb66c210eebe9fde6310760a5053</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27307985$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23439972$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Timm, Axel Eric</creatorcontrib><creatorcontrib>Nattland, Detlef</creatorcontrib><creatorcontrib>Schuster, Rolf</creatorcontrib><title>In situ determination of the surface excess upon electrochemical sulfate adsorption on Au(111) films by surface plasmon resonance</title><title>Physical chemistry chemical physics : PCCP</title><addtitle>Phys Chem Chem Phys</addtitle><description>For the independent and simultaneous characterization of electrochemical processes, we employ surface plasmon resonance (SPR) detection together with standard electrochemical methods. As a first test system we studied sulfate adsorption on Au(111). After careful calibration of the SPR signal we obtained submonolayer sensitivity on a millisecond time scale. The experimental data are simulated within the framework of a layer stack model of the optical interface. The sulfate adsorbate is simply described, employing the optical properties of sulfuric acid. The obtained potential dependent sulfate coverage is in reasonable agreement with independent results as presented in the literature.
We have studied sulfate adsorption and desorption processes on gold surfaces, employing time resolved surface plasmon generation.</description><subject>Adsorption</subject><subject>Calibration</subject><subject>Chemistry</subject><subject>Electrochemistry</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Mathematical models</subject><subject>Optical properties</subject><subject>Plasmons</subject><subject>Sulfates</subject><subject>Surface chemistry</subject><subject>Surface physical chemistry</subject><issn>1463-9076</issn><issn>1463-9084</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqN0UtLxDAQB_Agiu-LdyUeBBVWk06aNkcRXyB40XNJ0wlW-jLTgh795kZ23b2Jpwzkl3-YGcYOpLiQAsylAzcoBQJwjW1LpWFmRK7Wl3Wmt9gO0ZsQQqYSNtlWAgqMyZJt9vXQcarHiVc4Ymjrzo513_He8_EVOU3BW4ccPxwS8WmIV9igG0PvXrGtnW2iabwdkduK-jDMX3f8ajqVUp5xXzct8fJzGTU0ltoIAlLf2c7hHtvwtiHcX5y77OX25vn6fvb4dPdwffU4c2DycWaNVFCBKrV1MhExSmpQFnSmjHZJiqmpfFnqWEuBWKLxFWqQsXthU5HCLjud5w6hf5-QxqKtyWHT2A77iQoJOpWJUXnyDxpz81wbHen5nLrQEwX0xRDq1obPQoriZzvFajsRHy1yp7LFakl_1xHByQJYirP1IQ6oppXLQGQm_-nleO4CueXt6qNiqHw0h38Z-Aagy62k</recordid><startdate>20130514</startdate><enddate>20130514</enddate><creator>Timm, Axel Eric</creator><creator>Nattland, Detlef</creator><creator>Schuster, Rolf</creator><general>Royal Society of Chemistry</general><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>20130514</creationdate><title>In situ determination of the surface excess upon electrochemical sulfate adsorption on Au(111) films by surface plasmon resonance</title><author>Timm, Axel Eric ; Nattland, Detlef ; Schuster, Rolf</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c398t-a9143d34b6ac120ace1634a367496c25e59dfbb66c210eebe9fde6310760a5053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adsorption</topic><topic>Calibration</topic><topic>Chemistry</topic><topic>Electrochemistry</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Mathematical models</topic><topic>Optical properties</topic><topic>Plasmons</topic><topic>Sulfates</topic><topic>Surface chemistry</topic><topic>Surface physical chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Timm, Axel Eric</creatorcontrib><creatorcontrib>Nattland, Detlef</creatorcontrib><creatorcontrib>Schuster, Rolf</creatorcontrib><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Physical chemistry chemical physics : PCCP</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Timm, Axel Eric</au><au>Nattland, Detlef</au><au>Schuster, Rolf</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In situ determination of the surface excess upon electrochemical sulfate adsorption on Au(111) films by surface plasmon resonance</atitle><jtitle>Physical chemistry chemical physics : PCCP</jtitle><addtitle>Phys Chem Chem Phys</addtitle><date>2013-05-14</date><risdate>2013</risdate><volume>15</volume><issue>18</issue><spage>6667</spage><epage>6672</epage><pages>6667-6672</pages><issn>1463-9076</issn><eissn>1463-9084</eissn><abstract>For the independent and simultaneous characterization of electrochemical processes, we employ surface plasmon resonance (SPR) detection together with standard electrochemical methods. As a first test system we studied sulfate adsorption on Au(111). After careful calibration of the SPR signal we obtained submonolayer sensitivity on a millisecond time scale. The experimental data are simulated within the framework of a layer stack model of the optical interface. The sulfate adsorbate is simply described, employing the optical properties of sulfuric acid. The obtained potential dependent sulfate coverage is in reasonable agreement with independent results as presented in the literature.
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Adsorption Calibration Chemistry Electrochemistry Exact sciences and technology General and physical chemistry Mathematical models Optical properties Plasmons Sulfates Surface chemistry Surface physical chemistry |
title | In situ determination of the surface excess upon electrochemical sulfate adsorption on Au(111) films by surface plasmon resonance |
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