Mechanism study of enhanced electrochemical performance of ZrO2-coated LiCoO2 in high voltage region

被引:93
作者
Hwang, B. J. [1 ,2 ]
Chen, C. Y. [1 ]
Cheng, M. Y. [1 ]
Santhanam, R. [1 ]
Ragavendran, K. [1 ]
机构
[1] Natl Taiwan Univ Sci & Technol, Nanoelectrochem Lab, Dept Chem Engn, Taipei 106, Taiwan
[2] Natl Synchrotron Radiat Res Ctr, Hsinchu 300, Taiwan
关键词
Lithium cobalt oxide; Zirconia coating; Stability; High voltage; Lithium ion battery; Cathode; IN-SITU XRD; CAPACITY RETENTION; COBALT DISSOLUTION; CATHODE; STABILITY; BATTERIES;
D O I
10.1016/j.jpowsour.2010.01.040
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
In this study, the mechanism of enhanced performance of ZrO2-coated LiCoO2 especially at high potential range is systematically investigated. Firstly, when overcharging to 4.5 V (higher than 4.2 V. the normal cutoff charging potential), phase transformation from H1 to H2 takes place with less volume expansion for ZrO2-coated LiCoO2 (1.2% and 2.2% for as-received one). EIS analysis indicates the growth of interfacial impedance during charging/discharging can be effectively suppressed with ZrO2 coating on the LiCoO2 surface. It is demonstrated as well that cation mixing of the cycled LiCoO2 caused by re-intercalation of dissolved Co2+ is inhibited with the ZrO2 coating on the LiCoO2. Therefore the ZrO2-coated LiCoO2 shows great enhancement in the electrochemical properties with 85% capacity retention after 30 cycles from 3 to 4.5 ZrO2 at a rate of 0.5C. Nevertheless, under the same evaluation process, the as-received LiCoO2 possesses only 21% capacity retention, which is resulted from the formation of polymeric layers by the electrolyte decomposition on its surface, the higher volumetric changes during charging/discharging and possible cation mixing by re-intercalation of the dissolved Co2+. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:4255 / 4265
页数:11
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