电解质
腐蚀
钝化
材料科学
碳酸乙烯酯
铝
集电器
电化学
锂(药物)
电流密度
无机化学
化学工程
冶金
复合材料
化学
电极
物理化学
工程类
医学
物理
图层(电子)
量子力学
内分泌学
作者
Zijie Yuan,Yongjing Wang,Yaqi Chen,Xiaodong Zhu,Shizhao Xiong,Zhongxiao Song
标识
DOI:10.1002/cssc.202400164
摘要
Abstract Cycling aging is the one of the main reasons affecting the lifetime of lithium‐ion batteries and the contribution of aluminum current collector corrosion to the ageing is not fully recognized. In general, aluminum is corrosion resistant to electrolyte since a non‐permeable surface film of alumina is naturally formed. However, corrosion of aluminum current collector can still occur under certain conditions such as lithium bis(fluorosulfonyl)imide (LiFSI)‐based electrolyte or high voltage. Herein, we investigates the corrosion of aluminum current collector in the electrolyte of 1.2 M LiFSI in ethylene carbonate (EC) and ethyl methyl carbonate (EMC) mixed solvents. The electrochemical results shows that the corrosion current of aluminum is enhanced by cycling time and potential, which is correlated with the surface species and morphology. The formation of AlF 3 , which is induced by deep penetration of F − anions through surface passivation film, leads to internal volume change and the surface crack in the end. Our work will be inspiring for future development of high‐energy‐density and high‐power‐density lithium‐ion batteries in which the LiFSI salt will be intensively used.
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