Crack-induced abrupt capacity degradation in commercial LiNi0.8Co0.1Mn0.1O2 (NCM811)/SiOx-graphite pouch batteries

被引:0
|
作者
Zhang, Xianying [1 ,2 ]
Wang, Qiyu [1 ,2 ]
Li, Yu [1 ,2 ,3 ]
Sun, Guochen [1 ,3 ]
Yu, Xiqian [1 ,2 ,3 ]
Li, Hong [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Beijing Key Lab New Energy Mat & Devices, Inst Phys, Beijing 100190, Peoples R China
[2] Chinese Acad Sci, Inst Phys, Beijing Frontier Res Ctr Clean Energy, Huairou Div, Beijing 101400, Peoples R China
[3] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
关键词
LITHIUM-ION BATTERIES; DIFFERENTIAL VOLTAGE ANALYSES; COMPOSITE POSITIVE ELECTRODE; HIGH-POWER; NI-RICH; STRUCTURAL EVOLUTION; CELLS; MECHANISM; FADE;
D O I
10.1039/d4ra01738b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Reasons for abrupt capacity fading in commercial LiNi0.8Co0.1Mn0.1O2 (NCM811)/SiOx-graphite pouch batteries were evaluated using electrochemical methods. These approaches consist of charge and discharge curves, differential curves and electrochemical impedance spectroscopy (EIS), and some advanced verification techniques constituting scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). The predominance testament concerning capacity attenuation through experimental verification after the battery is disassembled proves that the silicon-based anode material deteriorates further, bringing about a significant number of cracks with the progression of cycles. In addition, electrolyte enters into the cracks, generating the excessive growth of the solid electrolyte interface (SEI) and the expansion of impedance, which eventually causes the failure of conductive networks, dilemma of ion transmission and increment in polarization, ultimately contributing to lithium dendrites.
引用
收藏
页码:19116 / 19123
页数:8
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