Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/49634

TítuloBinary Ce(III) and Li(I) triflate salt composition for solid polymer electrolytes
Autor(es)Alves, Raquel Diana Carneiro
Sabadini, R. C.
Silva, I. D. A.
Donoso, J. P.
Magon, C. J.
Pawlicka, Agnieszka
Silva, Maria Manuela
Palavras-chaveSolid polymer electrolytes
Chitosan
Cerium triflate
Lithium triflate
Mixed salt
Data2018
EditoraSpringer Verlag
RevistaIonics
Resumo(s)This study describes the results of the characterization of solid polymer electrolytes using chitosan matrix plasticized with glycerol and doped with cerium and lithium triflates binary salt composition. The electrolytes were prepared by solvent casting method and characterized by thermal analysis (thermogravimetric analysis - TGA and differential scanning calorimetry - DSC), impedance measurements, X-ray diffraction (XRD), scanning electron microscopy (SEM), atomic force microscopy (AFM), and electron paramagnetic resonance (EPR). Samples are thermally stable up to 128-153ºC and most of them are amorphous. In some cases, the appearance of crystalline peaks is due to the diffraction of salt domains, which makes the samples less conductive. The room temperature conductivity maximum of 10-6 S cm-1 at 30ºC was obtained for the samples with the same total salts mass of 0.15 g (ChitCeTrif0.05LiTrif0.10 and ChitCeTrif0.10LiTrif0.05). Finally, the EPR analysis suggests that the local coordination environment of the paramagnetic Ce3+ is not the same in different samples. In summary, beside the modest conductivity values of these samples, they are still adequate for some electrochemical applications.
TipoArtigo
URIhttps://hdl.handle.net/1822/49634
DOI10.1007/s11581-017-2355-8
ISSN0947-7047
e-ISSN1862-0760
Arbitragem científicayes
AcessoAcesso restrito UMinho
Aparece nas coleções:CDQuim - Artigos (Papers)

Ficheiros deste registo:
Ficheiro Descrição TamanhoFormato 
Binary Ce(III) and Li(I) Triflates Salt Composition for Solid Polymer Electrolytes.pdf
Acesso restrito!
1,58 MBAdobe PDFVer/Abrir

Este trabalho está licenciado sob uma Licença Creative Commons Creative Commons

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