电极
材料科学
石墨
阳极
电化学
多孔性
复合材料
断层摄影术
分析化学(期刊)
自行车
化学
放射科
色谱法
医学
历史
物理化学
考古
作者
H. Michael,Francesco Iacoviello,Thomas M. M. Heenan,Alice V. Llewellyn,Julia S. Weaving,Rhodri Jervis,Dan J. L. Brett,Paul R. Shearing
出处
期刊:Journal of The Electrochemical Society
[The Electrochemical Society]
日期:2020-12-23
卷期号:168 (1): 010507-010507
被引量:47
标识
DOI:10.1149/1945-7111/abd648
摘要
Graphite is the most commonly used anode material in commercial lithium-ion batteries (LiBs). Understanding the mechanisms driving the dimensional changes of graphite can pave the way to methods for inhibiting degradation pathways and possibly predict electrochemical performance loss. In this study, correlative microscopy tools were used alongside electrochemical dilatometry (ECD) to provide new insights into the dimensional changes during galvanostatic cycling. X-ray computed tomography (CT) provided a morphological perspective of the cycled electrode so that the effects of dilation and contraction on effective diffusivity and electrode pore phase volume fraction could be examined. During the first cycle, the graphite electrode underwent thickness changes close to 9% after lithiation and, moreover, it did not return to its initial thickness after subsequent delithiation. The irreversible dilation increased over subsequent cycles. It is suggested the primary reason for this dilation is electrode delamination. This is supported by the finding that the electrode porosity remained mostly unchanged during cycling, as revealed by X-ray CT.
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