电解质
法拉第效率
盐(化学)
水溶液
钝化
电池(电)
溶解
无机化学
化学
阳极
阴极
氧化物
化学工程
材料科学
电极
有机化学
物理化学
物理
功率(物理)
量子力学
图层(电子)
工程类
作者
Kee Wah Leong,Wending Pan,Yifei Wang,Shijing Luo,Xiaolong Zhao,Dennis Y.C. Leung
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2022-07-21
卷期号:7 (8): 2657-2666
被引量:49
标识
DOI:10.1021/acsenergylett.2c01255
摘要
Rechargeable Mg batteries are a promising post-Li-ion battery technology, but their development has been critically hampered by the passivating nature of Mg, particularly in aqueous solutions. Due to a quick dismissal of its reversibility, the use of Mg anodes in aqueous electrolytes has been overlooked, and most researchers focus on nonaqueous systems instead. In this work, reversible, aqueous Mg battery chemistry has been realized for the first time, via the conversion of its impermeable passivation film to a conductive metallic oxide complex, facilitated by Cl– regulation and the suppression of the hydrogen evolution reaction using a MgCl2 water-in-salt (WIS) electrolyte. When coupled with copper hexacyanoferrate as the cathode, the full battery exhibits an impressive voltage plateau of 2.4–2.0 V and a stability of over 700 cycles with a Coulombic efficiency of up to 99% at 0.5 A g–1. Mg dissolution and deposition have proven reversible in the aqueous MgCl2 WIS electrolyte.
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