粒子(生态学)
材料科学
原位
自行车
化学物理
电池(电)
电极
降级(电信)
相(物质)
航程(航空)
人口
纳米颗粒
纳米技术
化学工程
化学
热力学
物理化学
物理
复合材料
地质学
计算机科学
社会学
电信
历史
海洋学
有机化学
考古
功率(物理)
工程类
人口学
作者
Yahong Xu,Enyuan Hu,Kai Zhang,Xuelong Wang,V. Borzenets,Zhihong Sun,P. Pianetta,Xiqian Yu,Yijin Liu,Xiao‐Qing Yang,Hong Li
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2017-05-05
卷期号:2 (5): 1240-1245
被引量:202
标识
DOI:10.1021/acsenergylett.7b00263
摘要
For designing new battery systems with higher energy density and longer cycle life, it is important to understand the degradation mechanism of the electrode material, especially at the individual particle level. Using in situ transmission X-ray microscopy (TXM) coupled to a pouch cell setup, the inhomogeneous Li distribution as well as the formation, population, and evolution of inactive domains in a single LiCoO<sub>2</sub> particle were visualized in this paper as it was cycled for many times. It is found that the percentage of the particle that fully recovered to the pristine state is strongly related to the cycling rate. Interestingly, we also observed the evolution of the inactive region within the particle during long-term cycling. The relationship between morphological degradation and chemical inhomogeneity, including the formation of unanticipated Co metal phase, is also observed. Finally, our work highlights the capability of in situ TXM for studying the degradation mechanism of materials in LIBs.
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