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Synthetic strategies for better battery performance through advances in materials and chemistry: Olivine LiMn1/3Co1/3Ni1/3PO4
被引:10
作者:
Minakshi, Manickam
[1
]
Kandhasamy, Sathiyaraj
[1
]
Meyrick, Danielle
[1
]
机构:
[1] Murdoch Univ, Fac Minerals & Energy, Murdoch, WA 6150, Australia
基金:
澳大利亚研究理事会;
关键词:
LiMn1/3Co1/3Ni1/3PO4;
Sol-gel;
Combustion;
LiOH;
Aqueous battery;
Synthesis;
COMBUSTION SYNTHESIS;
ELECTROCHEMICAL PERFORMANCE;
ELECTRODE MATERIALS;
PHOSPHO-OLIVINES;
CATHODE;
FE;
NI;
CO;
D O I:
10.1016/j.jallcom.2012.07.136
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070305 [高分子化学与物理];
摘要:
Olivine LiMn1/1Co1/1Ni1/3PO4 powder synthesized via wet chemistry route sol-gel and combustion showed desirable features like reduced particles size with conductive coatings on the surface and well cation ordering with respect to the traditional solid state reaction. The morphological homogeneity is achieved through complexing agents employed (chelating agent/fuel) resulting in high pure material even for substitution of multi divalent cations (Co and Mn) for Ni in LiNiPO4. The low sintering temperature prevents the particle agglomeration without any compromise on the degree of crystallinity. The experimental conditions are very similar for both sol-gel and combustion, except for the reaction inducers (chelating agent and fuel) that influenced the composition and the particle size between them. The mixed transition-metal olivine (LiMn1/1Co1/1Ni1/3PO4) cathodes synthesized by sal-gel and combustion methods are compared and their electrochemical properties are discussed. Structural analyses of the synthesized samples showed substitution of mixed cations crystallizes in the olivine structure. The improved morphology achieved for combustion synthesis resulted in better specific capacity with good capacity retention than for the sal-gel counterpart. (C) 2012 Elsevier B.V. All rights reserved.
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页码:62 / 66
页数:5
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