The mechanism of side reaction induced capacity fading of Ni-rich cathode materials for lithium ion batteries

被引:0
|
作者
Hu D. [1 ,3 ]
Su Y. [1 ,2 ]
Chen L. [1 ,2 ]
Li N. [1 ,2 ]
Bao L. [1 ]
Lu Y. [1 ,2 ]
Zhang Q. [1 ,2 ]
Wang J. [1 ,2 ]
Chen S. [1 ]
Wu F. [1 ,2 ]
机构
[1] School of Materials Science and Engineering, Beijing Key Laboratory of Environmental Science and Engineering, Beijing Institute of Technology, Beijing
[2] Beijing Institute of Technology Chongqing Innovation Center, Chongqing
[3] China North Vehicle Research Institute, Beijing
来源
Chen, Lai (chenlai144@sina.com) | 1600年 / Elsevier B.V.卷 / 58期
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Failure mechanism; HF erosion; LiF deposition; Lithium-ion batteries; Ni-rich cathode materials;
D O I
10.1016/j.jechem.2020.09.031
中图分类号
学科分类号
摘要
Ni-rich cathode materials show great potential of applying in high-energy lithium ion batteries, but their inferior cycling stability hinders this process. Study on the electrode/electrolyte interfacial reaction is indispensable to understand the capacity failure mechanism of Ni-rich cathode materials and further address this issue. This work demonstrates the domain size effects on interfacial side reactions firstly, and further analyzes the inherent mechanism of side reaction induced capacity decay through comparing the interfacial behaviors before and after MgO coating. It has been determined that LiF deposition caused thicker SEI films may not increase the surface film resistance, while HF erosion induced surface phase transition will increase the charge transfer resistance, and the later plays the dominant factor to declined capacity of Ni-rich cathode materials. This work suggests strategies to suppress the capacity decay of layered cathode materials and provides a guidance for the domain size control to match the various applications under different current rates. © 2020
引用
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页码:1 / 8
页数:7
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