IMN

Biblio. IMN

Référence en vue solo

Jimenez, P., Levillain, E., Aleveque, O., Guyomard, D., Lestriez, B. & Gaubicher, J. (2017) Lithium n-Doped Polyaniline as a High-Performance Electroactive Material for Rechargeable Batteries. Angew. Chem.-Int. Edit. 56 1553–1556. 
Added by: Richard Baschera (2017-03-23 10:23:25)   Last edited by: Richard Baschera (2017-03-23 10:24:47)
Type de référence: Article
DOI: 10.1002/anie.201607820
Numéro d'identification (ISBN etc.): 1433-7851
Clé BibTeX: Jimenez2017
Voir tous les détails bibliographiques
Catégories: ST2E
Mots-clés: conducting polymers, energy-storage, films, lithium ion batteries, organic active materials, organic electrode, polyaniline, spectroelectrochemistry
Créateurs: Aleveque, Gaubicher, Guyomard, Jimenez, Lestriez, Levillain
Collection: Angew. Chem.-Int. Edit.
Consultations : 1/600
Indice de consultation : 5%
Indice de popularité : 1.25%
Résumé     
The discovery of conducting lithium-doped polyaniline with reversible redox chemistry allows simultaneous unprecedented capacity and stability in a non-aqueous Li battery. This compound (lithium emeraldinate) was synthesized by lithium-proton exchange on the emeraldine base in an anhydrous lithium-based electrolyte. A combination of UV/Vis-NIR spectroelectrochemistry, XPS, FTIR, and EQCM characterization allowed a unified description of the chemical and electrochemical behavior, showing facile charge delocalization of the doped states and the reversibility of the redox processes in this form of polyaniline. From a practical point of view, lithium emeraldinate behaves as a high-capacity organic active material (230mAhg(-1)) that enables preparation of relatively thick composite electrodes with a low amount of carbon additives and high energy density (460Whkg(-1)). Concomitantly, at 1C rate, 400 cycles were achieved without significant capacity loss, while the coulombic efficiency is greater than 99%.
  
wikindx 4.2.2 ©2014 | Références totales : 2856 | Requêtes métadonnées : 56 | Exécution de script : 0.13169 secs | Style : Harvard | Bibliographie : Bibliographie WIKINDX globale