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.
引用
收藏
页码:1972 / 1981
页数:10
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