Dubarry, M., Gaubicher, J., Guyomard, D., Wallez, G., Quarton, M. & Baehtz, C. (2008) Uncommon potential hysteresis in the Li/Li2xVO(H2-xPO4)2 (0 <= x <= 2) system. Electrochim. Acta, 53 4564–4572.
Added by: Laurent Cournède (2016-03-10 21:58:42) |
Type de référence: Article DOI: 10.1016/j.electacta.2007.12.085 Numéro d'identification (ISBN etc.): 0013-4686 Clé BibTeX: Dubarry2008 Voir tous les détails bibliographiques |
Catégories: ST2E Mots-clés: 4 v, Cathodes, insertion, ionic exchange, li3fe2(po4)(3), Lithium batteries, lithium intercalation, optimization, positive-electrode materials, potential hysteresis, vanadium phosphate Créateurs: Baehtz, Dubarry, Gaubicher, Guyomard, Quarton, Wallez Collection: Electrochim. Acta |
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Résumé |
Physical and electrochemical investigations of vanadium phosphates, Li2xVO(H2-xPO4)(2) (0 {<} x {<} 2), havebeen undertaken. H+/Li+ ionic exchange from VO(H2PO4)(2) to Li2VO(HPO4)(2) leads to grain decrepitation. Further ionic exchange toward formation of Li4VO(PO4)(2) lowers the symmetry. As inferred from potentiodynamic cycling correlated to exsitu and in situ X-ray diffraction (XRD), the system Li/Li4VO(PO4)(2) shows several phase transformations that are associated with thermodynamical potential hysteresis that span from roughly 15 mV to more than 1.8 V. Small hysteresis are associated with topotactic reactions and with V-v/V-Iv and V-III/V-II redox couples. Large potential hysteresis values ({>} 1 V) were observed when oxidation of V-III to V-IV is involved. (c) 2008 Elsevier Ltd. All rights reserved.
Added by: Laurent Cournède |