Nanocrystalline LiFePO4 was obtained by heating amorphous nanosized LiFePO4. The amorphous material was obtained by lithiation of FePO4 synthesized by spontaneous precipitation from equimolar aqueous solutions of Fe( NH4)(2) (SO4) (2).6H(2)O and NH4H2PO4, using hydrogen peroxide as the oxidizing agent. The materials were characterized by chemical analysis, thermogravimetric and differential thermal analysis, X-ray powder diffraction, and scanning electron microscopy. The Brunauer-Emmett-Teller method was used to evaluate the specific surface area. Nanocrystalline LiFePO4 showed very good electrochemical performance delivering about the full theoretical capacity (170 Ah kg(-1)) when cycled at the C/10 rate. A capacity fade of about 0.25% per cycle affected the material upon cycling. (C) 2002 The Electrochemical Society.
A new synthetic route for preparing LiFePO4 with enhanced electrochemical performance / Prosini, P. P.; Carewska, M.; Scaccia, S.; Wisniewski, P.; Passerini, S.; Pasquali, Mauro. - In: JOURNAL OF THE ELECTROCHEMICAL SOCIETY. - ISSN 0013-4651. - STAMPA. - 149:(2002), pp. A886-A890. [10.1149/1.1481716]
A new synthetic route for preparing LiFePO4 with enhanced electrochemical performance
S. Passerini;PASQUALI, Mauro
2002
Abstract
Nanocrystalline LiFePO4 was obtained by heating amorphous nanosized LiFePO4. The amorphous material was obtained by lithiation of FePO4 synthesized by spontaneous precipitation from equimolar aqueous solutions of Fe( NH4)(2) (SO4) (2).6H(2)O and NH4H2PO4, using hydrogen peroxide as the oxidizing agent. The materials were characterized by chemical analysis, thermogravimetric and differential thermal analysis, X-ray powder diffraction, and scanning electron microscopy. The Brunauer-Emmett-Teller method was used to evaluate the specific surface area. Nanocrystalline LiFePO4 showed very good electrochemical performance delivering about the full theoretical capacity (170 Ah kg(-1)) when cycled at the C/10 rate. A capacity fade of about 0.25% per cycle affected the material upon cycling. (C) 2002 The Electrochemical Society.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
