四氢呋喃
过电位
锌
法拉第效率
电解质
氢键
化学
成核
水溶液
阳极
氢
化学工程
电池(电)
电偶阳极
制氢
无机化学
材料科学
甲醇
钝化
塔菲尔方程
电化学
腐蚀
钾离子电池
锌化合物
金属
键能
分子
作者
Bingjie Zhang,Zenglong Xu,Y. Le Du,Guilan Duan,Degang Zhao,Bingqiang Cao,Shuhua Yang
摘要
Aqueous zinc-ion batteries (AZIBs) have emerged as a promising candidate for large-scale energy storage. However, the hydrogen evolution reaction (HER) is a key factor affecting the stability of zinc anodes. Here, a tetrahydrofuran (THF)-mediated hydrogen bonding strategy is adopted to develop a THF-based electrolyte (ZS-T electrolyte), in which strong hydrogen bonds between THF and H2O molecules block the transmission of protons in water to inhibit the HER, thereby improving the stability of zinc anodes. Therefore, the corrosion rate of zinc anode decreases to 3.40 × 10-5 A cm-2 in the optimized ZS-T-5 electrolyte, and the zinc nucleation overpotential drops to 28.97 mV. The Zn//Zn symmetric battery cycled for over 1000 hours at 1 mA cm-2; the Zn//Cu half-cell cycled 1000 times with an average coulombic efficiency of 99.32%; and the Zn//MnO2 full cell cycled 800 times at 1 A g-1, with the capacity retention rate increasing from 34.1% to 63.3%.
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