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Structural, spectroscopic and magnetic investigation of the LiFe1-xMnxPO4 (x=0-0.18) solid solution
被引:37
作者:
Bini, Marcella
[1
]
Mozzati, Maria Cristina
[2
]
Galinetto, Pietro
[2
]
Capsoni, Doretta
[1
]
Ferrari, Stefania
[1
]
Grandi, Marco S.
[2
]
Massarotti, Vincenzo
[1
]
机构:
[1] Univ Pavia, Dept Phys Chem M Rolla, I-27100 Pavia, Italy
[2] Univ Pavia, Dept Phys A Volta, CNISM, I-27100 Pavia, Italy
关键词:
LiFePO4;
EPR;
Magnetization;
XRPD;
Micro-Raman;
Impurity phases;
Cation distribution;
X-RAY-DIFFRACTION;
ELECTROCHEMICAL PERFORMANCE;
PHOSPHO-OLIVINES;
LIMPO4;
M;
LIFEPO4;
RAMAN;
TRIPHYLITE;
REDUCTION;
PYROLYSIS;
FE3+;
D O I:
10.1016/j.jssc.2009.05.016
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
Different solid state and sol-gel preparations of undoped and Mn substituted cathode material LiFePO4 ;re investigated. Li3PO4, Fe2P2O7 and Li4P2O7 are detected and quantified by XRPD only in solid state synthesis. In addition, micro-Raman spectra reveal low amount of different iron oxides Clusters. EPR data, combined with the results of magnetization measurements, evidence signals from Fe3+ ions in maghemite nanoclusters, and in Li3Fe2(PO4)(3). The sol-gel synthesis, showing the lowest amount of impurity phases, seems the most suitable to obtain a promising cathode material. The structural refinement gives new insights into the cation distribution of the Mn doped triphylite structure: (i) about 85% of Mn2+ ions Substitutes Fe2+, the remaining 15% being located on the Li site, thus suggesting a structural disorder also confirmed by EPR and micro-Raman results; (ii) Mn ions on the Li site are responsible for the observed slight cell volume expansion. (C) 2009 Elsevier Inc. All rights reserved.
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页码:1972 / 1981
页数:10
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