Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/44484

Registo completo
Campo DCValorIdioma
dc.contributor.authorCardoso, Marita A.por
dc.contributor.authorLeones, Rita Daniela Barrospor
dc.contributor.authorRodrigues, Luísa Cidália Guimarãespor
dc.contributor.authorFernandes, Marianapor
dc.contributor.authorFigueiredo, Filipe L.por
dc.contributor.authorNunes, Sílvia C.por
dc.contributor.authorSilva, Maria Manuelapor
dc.contributor.authorde Zea Bermudez, Verónicapor
dc.date.accessioned2017-01-26T12:19:50Z-
dc.date.issued2016-05-
dc.identifier.citationCardoso, M. A., Leones, R., Rodrigues, L., Fernandes, M., Figueiredo, F. L., Nunes, S. C., ... & De Zea Bermudez, V. C. (2016). Di‐ureasil hybrid electrolytes incorporating a new proton ionic liquid. ChemElectroChempor
dc.identifier.issn2196-0216por
dc.identifier.urihttps://hdl.handle.net/1822/44484-
dc.description.abstractThe protic ionic liquid (PIL) N-butylimidazolium trifluoromethanesulfonate ([BIm][TfO]) was obtained for the first time and incorporated into a sol-gel derived di-ureasil matrix with a concentration of X = 5, 10 and 30 %, where X is the ratio of the mass of PIL per mass of poly(oxyethylene) (POE). Four years after their synthesis, the resulting quasi-anhydrous electrolytes remained amorphous, homogeneous, flexible and thermally stable below 200 ºC. SEM/EDS data revealed the presence of the PIL at the surface of the xerogels with X > 5 %, demonstrating that this type of morphological characterization is mandatory to avoid misleading ionic conductivity values. The highest ionic conductivity was produced in the washed sample with X = 30 % (3.5 x10-5 and 2.1x10-3 S cm-1 at 25 and 170 ºC, respectively). The present family of electrolytes yielded higher conductivities than the N-ethylimidazolium trifluoromethanesulfonate-based analogues introduced earlier by our group and may be thus considered as promising candidates for applications in fuel cells.por
dc.description.sponsorshipFundação para a Ciência e a Tecnologia (FCT) and when applicable by FEDER under the PT2020 Partnership Agreement for financial support (contracts PTDC/CTM - BPC/112774/2009, UID/Multi/00709/2013, PEst - C/QUI/ UI0686/2013, PEst - OE/QUI/UI0616/2014 and FCT UID/CTM/50011/2013 ) and COST Action MP1202por
dc.language.isoengpor
dc.publisherWiley-VCH Verlagpor
dc.relationinfo:eu-repo/grantAgreement/FCT/5876-PPCDTI/112774/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/5876/147255/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/COMPETE/132953/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/5876/135918/PTpor
dc.relationinfo:eu-repo/grantAgreement/FCT/5876/147332/PTpor
dc.rightsrestrictedAccesspor
dc.subjectEletrólitos poliméricospor
dc.subjectLíquidos iónicospor
dc.subjectdi - ureasil hybridpor
dc.subjectElectrolytespor
dc.subjectN - butylimidazolium trifluoromethanesulfonate protic ionic liquidpor
dc.subjectFuel cellpor
dc.subjectconducting materialspor
dc.subjectdi-ureasil hybridspor
dc.subjectfuel cellspor
dc.subjectionic liquidspor
dc.titleDi-ureasil hybrid electrolytes incorporating a new proton ionic liquidpor
dc.typearticlepor
dc.peerreviewedyespor
dc.relation.publisherversionhttp://onlinelibrary.wiley.com/doi/10.1002/celc.201500557/abstractpor
sdum.publicationstatusinfo:eu-repo/semantics/publishedVersionpor
oaire.citationStartPage783por
oaire.citationEndPage789por
oaire.citationIssue5por
oaire.citationTitleChemElectroChempor
oaire.citationVolume3por
dc.identifier.eissn2196-0216por
dc.identifier.doi10.1002/celc.201500557por
dc.subject.fosCiências Naturais::Outras Ciências Naturaispor
dc.subject.wosScience & Technologypor
sdum.journalChemelectrochempor
Aparece nas coleções:CDQuim - Artigos (Papers)

Ficheiros deste registo:
Ficheiro Descrição TamanhoFormato 
Cardoso et al, ChemElectroChem.pdf
Acesso restrito!
1,34 MBAdobe PDFVer/Abrir

Partilhe no FacebookPartilhe no TwitterPartilhe no DeliciousPartilhe no LinkedInPartilhe no DiggAdicionar ao Google BookmarksPartilhe no MySpacePartilhe no Orkut
Exporte no formato BibTex mendeley Exporte no formato Endnote Adicione ao seu ORCID