Cathode materials modified by surface coating for lithium ion batteries

被引:552
作者
Li, C.
Zhang, H. P.
Fu, L. J.
Liu, H.
Wu, Y. P. [1 ]
Ram, E.
Holze, R.
Wu, H. Q.
机构
[1] Fudan Univ, Dept Chem, Shanghai 200433, Peoples R China
[2] Fudan Univ, Shanghai Key Lab Mol Catalysis & Innovat Mat, Shanghai 200433, Peoples R China
[3] Tech Univ Chemnitz, Inst Chem, AG Elektrochem, D-09111 Chemnitz, Germany
基金
中国国家自然科学基金;
关键词
lithium ion battery; surface modification; cathode materials; coating;
D O I
10.1016/j.electacta.2005.11.015
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Recent research results confirm the importance of structural surface features of cathode materials for their electrochemical performance. Modification by coating is an important method to achieve improved electrochemical performance, and the latest progress was reviewed here. When the surface of cathode materials including LiCoO2, LiNiO2, LiMn2O4 and LiMnO2 is coated with oxides such as MgO, Al2O3, SiO2, TiO2, ZnO, SnO2, ZrO2, Li2O center dot 2B(2)O(3)-glass and other materials, the coatings prevent the direct contact with the electrolyte solution, suppress phase transition, improve the structural stability, and decrease the disorder of cations in crystal sites. As a result, side reactions and heat generation during cycling are decreased. Accompanying actions such as suppression of Mn2+ dissolution, increase in conductivity and removal of HF in electrolyte solutions have been observed. Consequently, marked improvement of electrochemical performance of electrode materials including reversible capacity, coulomb efficiency in the first cycle, cycling behavior, rate capability and overcharge tolerance has been achieved. In conclusion, further directions are suggested for the surface modification of electrode materials. With further understanding of the effects of the surface structure of cathode materials on lithium intercalation and de-intercalation, better and/or cheaper cathode materials from surface modification will come up in the near future. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3872 / 3883
页数:12
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