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hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorDULUARD, Sandrine
hal.structure.identifierFraunhofer Institute for Silicate Research [Fraunhofer ISC]
dc.contributor.authorCELIK-COCHET, Ayse
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
hal.structure.identifierCollege of Sciences
dc.contributor.authorSAADEDDIN, Iyad
hal.structure.identifierSolems
dc.contributor.authorLABOURET, Anne
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.authorSCHOTTNER, Gerhard
hal.structure.identifierFraunhofer Institute for Silicate Research [Fraunhofer ISC]
dc.contributor.authorPOSSET, Uwe
hal.structure.identifierInstitut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
dc.contributor.authorDELVILLE, Marie-Hélène
dc.date.issued2011-07-15
dc.identifier.issn1144-0546
dc.description.abstractEnInorganic/organic (hybrid) complementary electrochromic devices (ECDs) of the type [transparent conducting oxide (TCO)//inorganic counter electrode/hydrophobic electrolytic membrane/polymeric working electrode//TCO] were assembled. The working electrodes consisted of spin-coated polymer films prepared by moderator-controlled in situ oxidative chemical polymerisation of 3{,}4-ethylene dioxythiophene (EDOT). Thin{,} galvanostatically deposited Prussian Blue (PB) films were employed as counter electrodes. Besides F : SnO2 (FTO)/glass and Sn : In2O3 (ITO)/glass{,} a flexible ITO/PET film was alternatively used for materials deposition. In order to attain the maximum device performance{,} the PB charge capacity was monitored and adapted to the capacity of the EDOT polymer films. The two electrochromic electrodes were separated by a novel hydrophobic polymer electrolyte based on a gel of 1-butyl-3-methyl-imidazolium bis (trifluoromethanesulfonyl)imide (BMI-TFSI) and poly(methylmethacrylate) (PMMA){,} with lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) as the salt. The influence of two parameters—ITO sheet resistance and the PMMA content in the electrolyte—on the final device properties was investigated. The ITO sheet resistance value proved to be crucial for the switching kinetics. The variation of the weight ratio of PMMA in the electrolyte showed that the effect on the kinetics is small whereas the change in absorbance is highly affected. The properties of the complementary glass-based devices were eventually compared to the corresponding plastic-based electrochromic elements. First attempts to scale up the technology were made for flexible 12 × 15 cm2 (active area) devices.
dc.language.isoen
dc.publisherRoyal Society of Chemistry
dc.subject.enElectrochromic
dc.subject.enPolymerised EDOT
dc.subject.enElectrochromic devices
dc.subject.enOxide
dc.subject.enElectrolyte
dc.subject.enPolymers
dc.subject.enPrussian blue
dc.subject.enPEDOT
dc.title.enElectrochromic devices based on in situ polymerised EDOT and Prussian Blue: influence of transparent conducting oxide and electrolyte composition—towards up-scaling
dc.typeArticle de revue
dc.identifier.doi10.1039/C1NJ20231F
dc.subject.halSciences de l'ingénieur [physics]/Génie des procédés
dc.subject.halSciences de l'ingénieur [physics]/Matériaux
bordeaux.journalNew Journal of Chemistry
bordeaux.page2314-2321
bordeaux.volume35
bordeaux.issue10
bordeaux.peerReviewedoui
hal.identifierhal-00627378
hal.version1
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00627378v1
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