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hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorDULUARD, Sandrine
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorOUVRARD, Blanche
hal.structure.identifierFraunhofer Institute for Silicate Research [Fraunhofer ISC]
dc.contributor.authorCELIK-COCHET, A.
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorCAMPET, Guy
hal.structure.identifierFraunhofer Institute for Silicate Research [Fraunhofer ISC]
dc.contributor.authorPOSSET, U.
hal.structure.identifierFraunhofer Institute for Silicate Research [Fraunhofer ISC]
dc.contributor.authorSCHOTTNER, G.
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorDELVILLE, Marie-Hélène
dc.date.issued2010
dc.identifier.issn1520-6106
dc.description.abstractEnThe performance of different poly(3,4-ethylenedioxythiophene) (PEDOT) films was compared by electrochemical, spectroelectrochemical, and time-derivative measurements of absorbance versus potential (linear potential-scan voltabsorptometry) for an overall spectroelectrochemical characterization of the electrochromic properties in ionic liquids such as 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (BMITFSI). The time-derivative signals were monitored at different wavelengths, and information obtained therefrom was complementary to that obtained from conventional cyclic voltammetry. PEDOT films prepared via in situ chemical oxidative polymerization appeared to be much more efficient than electropolymerized and PEDOT−poly(styrenesulfonate) (PSS) reference films, in terms of both contrast ratio and coloration efficiency, which was the case even for PEDOT films deposited on less conductive flexible plastic substrates.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.title.enComparison of PEDOT films obtained via three different routes through spectroelectrochemistry and the differential cyclic voltabsorptometry method (DCVA)
dc.typeArticle de revue
dc.identifier.doi10.1021/jp9111712
dc.subject.halChimie/Matériaux
bordeaux.journalJournal of Physical Chemistry B
bordeaux.page7445-7451
bordeaux.volume114
bordeaux.issue22
bordeaux.peerReviewedoui
hal.identifierhal-00491011
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00491011v1
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