In this paper the morphological, structural and electrochemical properties of crystalline lithium iron phosphate (LiFePO4) obtained from ferrous ammonium phosphate (FAP) have been studied. The FAP was obtained following four different processes, namely: (1) homogeneous phase precipitation, (2) heterogeneous phase precipitation from stoichiometric sodium phosphate, (3) heterogeneous phase precipitation from stoichiometric ammonium phosphate, and (4) heterogeneous phase precipitation from over stoichiometric ammonium phosphate. Lithium iron phosphate was prepared by solid state reaction of FAP with lithium hydroxide. In order to evaluate the effect of reaction time and synthesis temperature the LiFePO4 was prepared varying the heating temperatures (550, 600 and 700 C) and the reaction times (1 or 2 h). The morphology of the materials was evaluated by scanning electron microscopy while the chemical composition was determined by electron energy loss spectroscopy. X-ray diffraction was used to evaluate phase composition, crystal structure and crystallite size. The so obtained LiFePO4's were fully electrochemical characterized and a correlation was found between the crystal size and the electrochemical performance. © 2013 Elsevier Ltd. All rights reserved.

Effect of the synthesis conditions on the electrochemical properties of LiFePO4 obtained from NH4FePO4

Masci, A.;Carewska, M.;Cento, C.;Gislon, P.;Prosini, P.P.
2013

Abstract

In this paper the morphological, structural and electrochemical properties of crystalline lithium iron phosphate (LiFePO4) obtained from ferrous ammonium phosphate (FAP) have been studied. The FAP was obtained following four different processes, namely: (1) homogeneous phase precipitation, (2) heterogeneous phase precipitation from stoichiometric sodium phosphate, (3) heterogeneous phase precipitation from stoichiometric ammonium phosphate, and (4) heterogeneous phase precipitation from over stoichiometric ammonium phosphate. Lithium iron phosphate was prepared by solid state reaction of FAP with lithium hydroxide. In order to evaluate the effect of reaction time and synthesis temperature the LiFePO4 was prepared varying the heating temperatures (550, 600 and 700 C) and the reaction times (1 or 2 h). The morphology of the materials was evaluated by scanning electron microscopy while the chemical composition was determined by electron energy loss spectroscopy. X-ray diffraction was used to evaluate phase composition, crystal structure and crystallite size. The so obtained LiFePO4's were fully electrochemical characterized and a correlation was found between the crystal size and the electrochemical performance. © 2013 Elsevier Ltd. All rights reserved.
Thermogravimetric analysis (TGA);Electrochemical measurements;Sol-gel chemistry;Inorganic compounds;Electron microscopy
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/20.500.12079/1006
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