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Electrocatalysis of 2,5-Dimercapto-1,3,5-thiadiazole by 3,4-Ethylenedioxy-Substituted Conducting Polymers
The electronic properties of electropolymerized films of the 3,4-ethylenedioxy-substituted conducting polymers (CP) poly(3,4-ethylenedioxythiophene) (PEDOT), poly(3,4-ethylenedioxypyrrole) (PEDOP) and poly(3,4-ethylenedioxyselenophene) (PEDOS) have been investigated, along with their electrocatalyti...
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Published in: | Langmuir 2011-11, Vol.27 (22), p.13904-13909 |
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description | The electronic properties of electropolymerized films of the 3,4-ethylenedioxy-substituted conducting polymers (CP) poly(3,4-ethylenedioxythiophene) (PEDOT), poly(3,4-ethylenedioxypyrrole) (PEDOP) and poly(3,4-ethylenedioxyselenophene) (PEDOS) have been investigated, along with their electrocatalytic activity toward 2,5-dimercapto-1,3,4-thiadiazole (DMcT). For the electropolymerized films, the conductivity onset potential was most negative for PEDOP (−1.50 V), followed by PEDOS (−1.35 V) and with PEDOT possessing the most positive onset (−1.15 V). The heterogeneous charge transfer rate constant for DMcT in solution at polymer-film-modified glassy carbon electrodes (GCEs) was studied. It was found that compared to PEDOP, both PEDOS and PEDOT performed better as electrocatalysts, with PEDOS having a heterogeneous charge transfer rate constant of 1.8 × 10–3 cm/s. The film morphology of the electropolymerized films was investigated via SEM, and some film characteristics could be correlated with electrocatalytic activity. The potential use of CP/DMcT composites for lithium ion batteries (LIBs) is discussed. |
doi_str_mv | 10.1021/la202706s |
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For the electropolymerized films, the conductivity onset potential was most negative for PEDOP (−1.50 V), followed by PEDOS (−1.35 V) and with PEDOT possessing the most positive onset (−1.15 V). The heterogeneous charge transfer rate constant for DMcT in solution at polymer-film-modified glassy carbon electrodes (GCEs) was studied. It was found that compared to PEDOP, both PEDOS and PEDOT performed better as electrocatalysts, with PEDOS having a heterogeneous charge transfer rate constant of 1.8 × 10–3 cm/s. The film morphology of the electropolymerized films was investigated via SEM, and some film characteristics could be correlated with electrocatalytic activity. 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For the electropolymerized films, the conductivity onset potential was most negative for PEDOP (−1.50 V), followed by PEDOS (−1.35 V) and with PEDOT possessing the most positive onset (−1.15 V). The heterogeneous charge transfer rate constant for DMcT in solution at polymer-film-modified glassy carbon electrodes (GCEs) was studied. It was found that compared to PEDOP, both PEDOS and PEDOT performed better as electrocatalysts, with PEDOS having a heterogeneous charge transfer rate constant of 1.8 × 10–3 cm/s. The film morphology of the electropolymerized films was investigated via SEM, and some film characteristics could be correlated with electrocatalytic activity. The potential use of CP/DMcT composites for lithium ion batteries (LIBs) is discussed.</description><subject>Catalysis</subject><subject>Chemistry</subject><subject>Electrochemistry</subject><subject>Electrochemistry - methods</subject><subject>Electrochemistry: Charge Transfer, Electrocatalysis, Kinetics, Bioelectrochemistry</subject><subject>Ethylenes - chemistry</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Kinetics and mechanism of reactions</subject><subject>Microscopy, Electron, Scanning</subject><subject>Polymers - chemistry</subject><subject>Thiadiazoles - chemistry</subject><issn>0743-7463</issn><issn>1520-5827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNpt0F9rFDEUBfAgit1WH_oFZF6kFDZ682-yeSzrthUKCurzcDfJtCnZyZpkoOOnd6Tb9sWnA5cf58Ih5JTBJwacfY7IgWtoyyuyYIoDVSuuX5MFaCmolq04Isel3AOAEdK8JUecGaXA6AUJm-htzclixTiVUJrUN3yp6Jew89nivibKlmI-1LuALuCfFH2znRqxlHRT76boB-9Cepjoj3Fbaqhj9a5Zp8GNtobhtvme4jRXlXfkTY-x-PeHPCG_Ljc_19f05tvV1_XFDUUhZaVaCcOU167lvXMerINeO6sZ89o67LXaMttq0xpkrdK9AW3lCoSYw0tU4oScPfbuc_o9-lK7XSjWx4iDT2PpDPAVkwBylueP0uZUSvZ9t89hh3nqGHT_hu2eh53th0PruN159yyflpzBxwPAYjH2GQcbyouTWgHn7MWhLd19GvMwj_Gfh38BGJyLpg</recordid><startdate>20111115</startdate><enddate>20111115</enddate><creator>Rodríguez-Calero, Gabriel G</creator><creator>Lowe, Michael A</creator><creator>Burkhardt, Stephen E</creator><creator>Abruña, Héctor D</creator><general>American Chemical Society</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20111115</creationdate><title>Electrocatalysis of 2,5-Dimercapto-1,3,5-thiadiazole by 3,4-Ethylenedioxy-Substituted Conducting Polymers</title><author>Rodríguez-Calero, Gabriel G ; Lowe, Michael A ; Burkhardt, Stephen E ; Abruña, Héctor D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a344t-753915e7d62fdde0cd0f7dc711e7cdaf75b1c67969a1657f907c480337c4e4a53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Catalysis</topic><topic>Chemistry</topic><topic>Electrochemistry</topic><topic>Electrochemistry - methods</topic><topic>Electrochemistry: Charge Transfer, Electrocatalysis, Kinetics, Bioelectrochemistry</topic><topic>Ethylenes - chemistry</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Kinetics and mechanism of reactions</topic><topic>Microscopy, Electron, Scanning</topic><topic>Polymers - chemistry</topic><topic>Thiadiazoles - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rodríguez-Calero, Gabriel G</creatorcontrib><creatorcontrib>Lowe, Michael A</creatorcontrib><creatorcontrib>Burkhardt, Stephen E</creatorcontrib><creatorcontrib>Abruña, Héctor D</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Langmuir</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rodríguez-Calero, Gabriel G</au><au>Lowe, Michael A</au><au>Burkhardt, Stephen E</au><au>Abruña, Héctor D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electrocatalysis of 2,5-Dimercapto-1,3,5-thiadiazole by 3,4-Ethylenedioxy-Substituted Conducting Polymers</atitle><jtitle>Langmuir</jtitle><addtitle>Langmuir</addtitle><date>2011-11-15</date><risdate>2011</risdate><volume>27</volume><issue>22</issue><spage>13904</spage><epage>13909</epage><pages>13904-13909</pages><issn>0743-7463</issn><eissn>1520-5827</eissn><coden>LANGD5</coden><abstract>The electronic properties of electropolymerized films of the 3,4-ethylenedioxy-substituted conducting polymers (CP) poly(3,4-ethylenedioxythiophene) (PEDOT), poly(3,4-ethylenedioxypyrrole) (PEDOP) and poly(3,4-ethylenedioxyselenophene) (PEDOS) have been investigated, along with their electrocatalytic activity toward 2,5-dimercapto-1,3,4-thiadiazole (DMcT). For the electropolymerized films, the conductivity onset potential was most negative for PEDOP (−1.50 V), followed by PEDOS (−1.35 V) and with PEDOT possessing the most positive onset (−1.15 V). The heterogeneous charge transfer rate constant for DMcT in solution at polymer-film-modified glassy carbon electrodes (GCEs) was studied. It was found that compared to PEDOP, both PEDOS and PEDOT performed better as electrocatalysts, with PEDOS having a heterogeneous charge transfer rate constant of 1.8 × 10–3 cm/s. The film morphology of the electropolymerized films was investigated via SEM, and some film characteristics could be correlated with electrocatalytic activity. The potential use of CP/DMcT composites for lithium ion batteries (LIBs) is discussed.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>21955097</pmid><doi>10.1021/la202706s</doi><tpages>6</tpages></addata></record> |
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subjects | Catalysis Chemistry Electrochemistry Electrochemistry - methods Electrochemistry: Charge Transfer, Electrocatalysis, Kinetics, Bioelectrochemistry Ethylenes - chemistry Exact sciences and technology General and physical chemistry Kinetics and mechanism of reactions Microscopy, Electron, Scanning Polymers - chemistry Thiadiazoles - chemistry |
title | Electrocatalysis of 2,5-Dimercapto-1,3,5-thiadiazole by 3,4-Ethylenedioxy-Substituted Conducting Polymers |
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