Insight into the state of the ZrO2 coating on a LiCoO2 thin-film electrode using the ferrocene redox reaction

被引:18
作者
Inamoto, Jun-ichi [1 ]
Fukutsuka, Tomokazu [1 ,2 ]
Miyazaki, Kohei [1 ,2 ]
Abe, Takeshi [1 ,2 ]
机构
[1] Kyoto Univ, Grad Sch Engn, Nishikyo Ku, Kyoto 6158510, Japan
[2] Kyoto Univ, Hall Global Environm Res, Nishikyo Ku, Kyoto, Kyoto, Japan
关键词
LiCoO2 thin-film electrode; ZrO2; coating; Ferrocene redox reaction; Degradation mechanism; Surface electron conductivity; RAY-ABSORPTION SPECTROSCOPY; LI-ION CELL; ELECTRODE/ELECTROLYTE INTERFACE; LITHIUM BATTERIES; CATHODE MATERIAL; COBALT OXIDE; INTERCALATION; LIXCOO2; TEMPERATURE; DIFFRACTION;
D O I
10.1007/s10800-017-1121-y
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Metal oxide coating on positive active materials in lithium-ion batteries is an effective way to improve its cycleability. However, coating state of the metal oxide layer and the mechanism of the improvement have not been fully understood. In this paper, the coated state of ZrO2 on a LiCoO2 thin-film electrode was investigated using a ferrocene redox reaction, and the role of the ZrO2-coating on the degradation phenomena of the LiCoO2 was investigated. The redox behavior of ferrocene revealed that the ZrO2 layer did not cover the entire surface area of LiCoO2, that is, the ZrO2 layer was not compact and contained cracks. In addition, a lithium-ion deficit phase (Li1-x CoO2) was irreversibly formed on the uncovered LiCoO2 areas. In spite of the imperfect ZrO2 layer, the formation of the lithium-ion deficit phase inside the bulk was suppressed. It is clarified that a partial ZrO2 coating on the LiCoO2 is sufficient to suppress the growth of the lithium-ion deficit phase inside the bulk of LiCoO2.
引用
收藏
页码:1203 / 1211
页数:9
相关论文
共 27 条
[1]   Cobalt dissolution in LiCoO2-based non-aqueous rechargeable batteries [J].
Amatucci, GG ;
Tarascon, JM ;
Klein, LC .
SOLID STATE IONICS, 1996, 83 (1-2) :167-173
[2]   On the capacity fading of LiCoO2 intercalation electrodes:: the effect of cycling, storage, temperature, and surface film forming additives [J].
Aurbach, D ;
Markovsky, B ;
Rodkin, A ;
Levi, E ;
Cohen, YS ;
Kim, HJ ;
Schmidt, M .
ELECTROCHIMICA ACTA, 2002, 47 (27) :4291-4306
[3]   Effect of a ZrO2 coating on the structure and electrochemistry of LixCoO2 when cycled to 4.5 V [J].
Chen, ZH ;
Dahn, JR .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2002, 5 (10) :A213-A216
[4]   Comparison of Al2O3- and AlPO4-coated LiCoO2 cathode materials for a Li-ion cell [J].
Cho, J ;
Kim, TG ;
Kim, C ;
Lee, JG ;
Kim, YW ;
Park, B .
JOURNAL OF POWER SOURCES, 2005, 146 (1-2) :58-64
[5]  
Cho J, 2001, ANGEW CHEM INT EDIT, V40, P3367, DOI 10.1002/1521-3773(20010917)40:18<3367::AID-ANIE3367>3.0.CO
[6]  
2-A
[7]   Structural studies on the effects of ZrO2 coating on LiCoO2 during cycling using in situ X-ray diffraction technique [J].
Chung, Kyung Yoon ;
Yoon, Won-Sub ;
McBreen, James ;
Yang, Xiao-Qing ;
Oh, Si Hyoung ;
Shin, Ho Chul ;
Cho, Won Il ;
Cho, Byung Won .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2006, 153 (11) :A2152-A2157
[8]   The cathode-electrolyte interface in the Li-ion battery [J].
Edström, K ;
Gustafsson, T ;
Thomas, JO .
ELECTROCHIMICA ACTA, 2004, 50 (2-3) :397-403
[9]   Hexagonal to cubic spinel transformation in lithiated cobalt oxide - TEM investigation [J].
Gabrisch, H ;
Yazami, R ;
Fultz, B .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2004, 151 (06) :A891-A897
[10]   THE RAMAN-SPECTRA OF CO3O4 [J].
HADJIEV, VG ;
ILIEV, MN ;
VERGILOV, IV .
JOURNAL OF PHYSICS C-SOLID STATE PHYSICS, 1988, 21 (07) :L199-L201