Biblio. IMN

Référence en vue solo

Dubarry, M., Gaubicher, J., Guyomard, D., Steunou, N., Livage, J., Dupre, N. & Grey, C. P. (2006) Synthesis of Li1+alpha V3O8 via a gel precursor: Part II, from xerogel to the anhydrous material. Chem. Mat. 18 629–636. 
Added by: Florent Boucher (2016-05-12 13:21:37)
Type de référence: Article
DOI: 10.1021/cm051508+
Numéro d'identification (ISBN etc.): 0897-4756
Clé BibTeX: Dubarry2006a
Voir tous les détails bibliographiques
Catégories: ST2E
Mots-clés: Cathode, electrochemical-behavior, Lithium batteries, liv3o8, mas, performance, v-51, v2o5-center-dot-nh(2)o gels
Créateurs: Dubarry, Dupre, Gaubicher, Grey, Guyomard, Livage, Steunou
Collection: Chem. Mat.
Consultations : 7/533
Indice de consultation : 0%
Indice de popularité : 0%
The synthesis of anhydrous Li1+aV3O8 from its xerogel has been studied by using thermodiffractometry and variable temperature V-51 magic-angle spinning NMR spectroscopy. Completion of dehydration leads to a sample characterized by a bimodal grain size distribution, the larger and smaller sized particles coming from the two components of the xerogel (liquid and solid components), respectively. The specific reactions undergone by these two components have been identified: the solid component gradually loses water by undergoing a series of phase transitions involving layered phases with decreasing water concentrations, the hewettite framework being maintained throughout the reaction, whereas in the case of the dried liquid component of the xerogel, the formation of anhydrous Li1+aV3O8 occurs through the decomposition of lithium vanadates, which is followed by the formation and then progressive dehydration of a hydrated hewettite structure. It is shown that the biphasic nature of the pristine Gel precursor has an impact on the electrochemical behavior of anhydrous Li1+aV3O8.
Added by: Florent Boucher  
wikindx 4.2.2 ©2014 | Références totales : 2801 | Requêtes métadonnées : 61 | Exécution de script : 0.11762 secs | Style : Harvard | Bibliographie : Bibliographie WIKINDX globale