电解质
剥离(纤维)
电镀(地质)
钝化
铝
材料科学
电化学
无机化学
图层(电子)
化学
化学工程
电极
冶金
复合材料
工程类
物理化学
地球物理学
地质学
作者
Fatemehsadat Rahide,Jackson Flowers,Junjie Hao,Helge S. Stein,Helmut Ehrenberg,Sonia Dsoke
标识
DOI:10.1149/1945-7111/ad1553
摘要
Conventional electrolytes for aluminum metal batteries are highly corrosive because they must remove the Al 2 O 3 layer to enable plating and stripping. However, such corrosiveness impacts the stability of all cell parts, thus hampering the real application of aluminum-metal batteries. The urea/NMA/Al(OTF) 3 electrolyte is a non-corrosive alternative to the conventional [EMImCl]: AlCl 3 ionic liquid electrolyte (ILE). Unfortunately, this electrolyte demonstrates poor Al plating/stripping, probably because (being not corrosive) it cannot remove the Al 2 O 3 passivation layer. This work proves that no plating/stripping occurs on the Al electrode despite modifying the Al surface. We highlight how urea/NMA/Al(OTF) 3 electrolyte and the state of the Al electrode surface impact the interphase layer formation and, consequently, the likelihood and reversibility of Al plating/stripping. We point up the requirement for carefully drying electrolyte mixture and components, as water results in hydrogen evolution reaction and creation of an insulating interphase layer containing Al(OH) 3 , AlF 3 , and re-passivated Al oxide, which finally blocks the path for the possible Al plating/stripping.
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