电解质
阴极
法拉第效率
阳极
无机化学
水溶液
钒
氧化钒
电化学
剥离(纤维)
电镀(地质)
电极
溶解
化学
化学工程
材料科学
有机化学
复合材料
工程类
物理化学
地质学
地球物理学
作者
Kuo Wang,Fangming Liu,Qianrui Li,Jiaqi Zhu,Tong Qiu,Xiaoxia Liu,Xiaoqi Sun
标识
DOI:10.1016/j.cej.2022.139577
摘要
Aqueous Zn batteries provide high safety and low cost. However, the Zn metal anode experiences various side reactions and dendritic growth in aqueous electrolytes. Herein, we regulate the interfaces at both Zn anode and vanadium oxide cathode in aqueous batteries with a high donor number electrolyte additive. The N-methylpyrrolidone (NMP) molecule with the donor number of 27.3 is introduced to the ZnSO4 electrolyte at the low concentration of 5 %. It preferentially adsorbs on both electrode surface and induces electrode–electrolyte interfaces composed of mixed organic and inorganic species. Thanks to the effective protection of solid-electrolyte interface (SEI) on Zn anode, the corrosions from electrolytes are inhibited, and 99.5 % coulombic efficiency of plating-stripping is realized. The Zn deposition behavior is also modified, which ensures uniform Zn growth and stable Zn plating-stripping for 1100 h. Meanwhile, the cathode-electrolyte interface (CEI) at the V6O13·H2O cathode effectively suppresses vanadium dissolution, and the capacity retention over cycling is enhanced. Our work presents an effective strategy to simultaneously promote the electrochemical performance of both electrodes in aqueous Zn batteries.
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