镁
电解质
氯化物
无机化学
阳极
电化学
化学
电镀(地质)
硼氢化
剥离(纤维)
材料科学
电极
有机化学
催化作用
复合材料
物理化学
地质学
地球物理学
作者
Raymond Horia,Dan Thien Nguyen,Alex Yong Sheng Eng,Zhi Wei Seh
标识
DOI:10.1002/batt.202200011
摘要
Abstract Conventional magnesium salts are generally considered to be passivating to the magnesium anode, hence chloride‐based electrolyte additives are often added to circumvent this issue. As a result, the performance of conventional magnesium salts has rarely been assessed in a chloride‐free system. This work provides a comparative study on the electrochemical performance and interfacial reaction of four commercially available magnesium salts with tetrabutylammonium borohydride as moisture scavenger. Magnesium bis(hexamethyldisilazide) was found to be the most reductively stable and enabled excellent magnesium plating/stripping without chloride additive. Investigation of the solid electrolyte interphase revealed a thin organic polyether layer that was conducive to magnesium‐ion migration. The results also showed that a minuscule amount of chloride (20 mM) improved the reversibility of magnesium plating/stripping but was still corrosive towards the current collector, thus establishing that chloride‐free electrolyte is most appropriate for future development of rechargeable magnesium batteries.
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