Cyclic performances of HT-LiCo0.8M0.2O2 (M=Al, Ni) powders prepared by the molten salt synthesis method
被引:21
作者:
Han, CH
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机构:Korea Univ, Dept Chem, Res Div Chem & Mol Engn, Sungbuk Gu, Seoul 136701, South Korea
Han, CH
Hong, YS
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机构:Korea Univ, Dept Chem, Res Div Chem & Mol Engn, Sungbuk Gu, Seoul 136701, South Korea
Hong, YS
Kim, K
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机构:
Korea Univ, Dept Chem, Res Div Chem & Mol Engn, Sungbuk Gu, Seoul 136701, South KoreaKorea Univ, Dept Chem, Res Div Chem & Mol Engn, Sungbuk Gu, Seoul 136701, South Korea
Kim, K
[1
]
机构:
[1] Korea Univ, Dept Chem, Res Div Chem & Mol Engn, Sungbuk Gu, Seoul 136701, South Korea
[2] Elect & Telecommun Res Inst, Power Source Device Team, Taejon 305350, South Korea
lithium ion battery;
LiCo0.8Al0.2O2;
LiCo0.8Ni0.2O2;
molten salt;
D O I:
10.1016/S0167-2738(02)00886-X
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Single phases of M-substituted lithium cobalt oxides, HT-LiCo0.8M0.2O2 (M=Al, Ni), were prepared by molten salt synthesis (MSS) method using coprecipitated Co-M hydroxides in 0.59 LiNO3-0.41 LiOH. The prepared powders consisted of well-developed particles with spherical shape and the particle size was around 150 nm in diameter. Among them, HT-LiCo0.8Al0.2O2 showed an inferior cyclic performance and a smaller discharge capacity than HT-LiCo0.8Ni0.2O2, even though the former is more structurally stable than the latter. Structural analysis of HT-LixCo0.8Al0.2O2 indicated that the Al substitution, causing an enhanced internal resistance for lithium ion diffusion, is responsible for the capacity fading. In the meanwhile, HT-LixCo0.8Ni0.2O2 with large c layer spacing showed as high as 146 mAh/g at the first cycle and 130 mAh/g at the twentieth cycle. (C) 2002 Elsevier Science B.V. All rights reserved.