涂层
腐蚀
电解质
材料科学
原电池
电偶腐蚀
阴极
冶金
芯(光纤)
石墨
开路电压
化学工程
复合材料
电压
化学
电极
物理化学
工程类
物理
量子力学
标识
DOI:10.1149/1945-7111/ad0c6b
摘要
Aluminum-coated (Al-Clad) coin cell case has long been introduced to evaluate high-voltage cathode materials and electrolytes in battery research. However, our study on graphite/LiNi 0.80 Co 0.10 Mn 0.10 O 2 (Gr/NCM811) coin cells indicates that the Al-Clad case resulted in even worse performance than the pristine stainless steel (SS) case. Post-mortem observation finds that the Al-Clad case was severely corroded, while the SS case seems to remain intact. To understand this unusual phenomenon, the corrosion behavior of the Al-Clad cases in LiPF 6 electrolyte and lithium bis(fluorosulfonyl)imide (LiFSI) electrolyte, respectively, is studied. It is shown that the coating of Al on the Al-Clad cases is not dense, allowing liquid electrolytes to permeate through and contact the underlying SS core case, forming galvanic cells between the Al coating and the SS core case. At high potentials, the galvanic cells reduce the over-potential of Al oxidation, promoting corrosion of the Al coating. As such, the Al coating does not protect the underlying SS core case, oppositely, making the corrosion of itself more severe. The results of this work reveal that to support high-voltage applications, the coating of Al on the Al-Clad cases must be dense, otherwise, it makes the corrosion worse.
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