Capacity fading mechanism during long-term cycling of over-discharged LiCoO2/mesocarbon microbeads battery

被引:103
|
作者
Zhang, Lingling [1 ]
Ma, Yulin [1 ]
Cheng, Xinqun [1 ]
Du, Chunyu [1 ]
Guan, Ting [1 ]
Cui, Yingzhi [1 ]
Sun, Shun [1 ]
Zuo, Pengjian [1 ]
Gao, Yunzhi [1 ]
Yin, Geping [1 ]
机构
[1] Harbin Inst Technol, Sch Chem Engn & Technol, Inst Adv Chem Power Sources, Harbin 15001, Peoples R China
基金
美国国家科学基金会;
关键词
LiCoO2/MCMB battery; Over-discharge; Long-term cycling; Capacity fading mechanism; LITHIUM-ION BATTERY; X-RAY-DIFFRACTION; HIGH-TEMPERATURE; HIGH-POWER; PERFORMANCE; ELECTRODES; OVERDISCHARGE; STABILITY; COMPOSITE; ABUSE;
D O I
10.1016/j.jpowsour.2015.06.040
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
The LiCoO2/mesocarbon microbeads (MCMB) batteries are over-discharged to 102% DOD, 105% DOD and 115% DOD, respectively, then are fully charged and cycled 1000 times at 0.6 C with 30% DOD. The capacity fading mechanism during long-term cycling of over-discharged batteries is analyzed by electrochemical and physical characterization. No remarkable difference is found on the morphology of LiCoO2 material from SEM. However, copper is detected on anode over-discharged to 115% DOD by EDS and XRD. The structures of LiCoO2 and MCMB materials have almost no change according to the result of XRD test. The performance of MCMB material can be degraded by over-discharge, however the LiCoO2 material still keeps good performance. The capacity of MCMB electrode is improved after being washed with water to remove the SEI film, indicating that the capacity loss of MCMB electrode is mainly attributed to the increase of SEI film. The capacity deterioration of over-discharged battery is mainly caused by the dissolution of copper current collector and the deposition of Cu on the surface of anode during the following charging process. The copper deposited on the surface of anode can hinder the lithium intercalation into/de-intercalation from the anode and promote the increase of SE! film. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:1006 / 1015
页数:10
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