Electrochemical AFM study of LiMn2O4 thin film electrodes exposed to elevated temperatures

被引:66
作者
Doi, Takayuki [1 ]
Inaba, Minoru [2 ]
Tsuchiya, Hiroshi [3 ]
Jeong, Soon-Ki [4 ]
Iriyama, Yasutoshi [3 ]
Abe, Takeshi [3 ]
Ogumi, Zempachi [3 ]
机构
[1] Kyushu Univ, Inst Mat Chem & Engn, Kasuga, Fukuoka 8168580, Japan
[2] Doshisha Univ, Fac Engn, Dept Mol Sci & Technol, Kyoto 6100321, Japan
[3] Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan
[4] Soonchunhyang Univ, Dept Chem Engn, Asan 336745, Chungnam, South Korea
关键词
lithium-ion battery; lithium manganese oxide; capacity fading; atomic force microscopy; surface morphology;
D O I
10.1016/j.jpowsour.2008.02.054
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
Surface morphology changes of LiMn2O4 thin film positive electrodes in lithium-ion batteries after repeated potential cycling or storage at elevated temperatures were observed by in situ atomic force microscopy (AFM) to elucidate the origin of capacity fading of LiMn2O4. After repeated potential cycling in the overall potential range from 3.50 to 4.30 V at elevated temperatures, the entire thin film surface was covered with small round-shaped particles accompanied by capacity fading of the electrode, while no significant changes were observed at 25 degrees C. The discharge capacity decreased more significantly when cycled in the lower potential range (3.81-4.07 V) than when cycled in the higher potential range (4.04-4.30 V). After storage at elevated temperatures at a depth of discharge (DOD) of 75%, which is located in the lower potential range, similar surface morphology changes were observed. In addition, discharge capacity markedly decreased, and the crystallinity of the LiMn2O4 thin film was lowered after storage. Hence, the observed changes in morphology at elevated temperatures are closely related to capacity fading of the LiMn2O4 thin film. The loss of crystallinity was caused by the formation of small particles on the LiMn2O4 surface, which would be accelerated on the LiMn2O4 surface in contact with an electrolyte solution through some kind of dissolution/precipitation reaction.
引用
收藏
页码:539 / 545
页数:7
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