电解质
材料科学
阳极
电介质
钝化
水溶液
吸附
化学工程
锌
分子
无机化学
图层(电子)
纳米技术
电极
冶金
化学
有机化学
物理化学
光电子学
工程类
作者
Kangkang Bao,Minghui Wang,Yue Zheng,Panpan Wang,Liwen Yang,Yang Jin,Hui Wu,Bin Sun
出处
期刊:Nano Energy
[Elsevier BV]
日期:2023-11-16
卷期号:120: 109089-109089
被引量:17
标识
DOI:10.1016/j.nanoen.2023.109089
摘要
Zinc (Zn) metal-based aqueous batteries are attracting tremendous attention facing grid-energy storage. However, the practical application has been severely impeded due to the challenges of Zn anode including the dendrites growth, side reactions and passivation layer accumulation. Here, an accessible solvent (ethanol, ETH) with low dielectric constant is utilized as an electrolyte additive to modulate the coordination environment of Zn2+ and the surface of Zn anode. The new assembled solvated ions reduce the inherent electrostatic interactions within the overall electrolyte, resulting in the efficient migration of Zn2+. In addition, the preferential adsorption of ETH on the Zn surface leads to the formation of an improved electric double layer (EDL), which effectively restricts water molecule access and regulates unique transfer channels of Zn2+. As a result, dense deposit with orientation plating is achieved. Zn||MnO2 full cells disclose an impressive capacity retention of 84.47% even after undergoing 2000 cycles at a high current density of 1 A g-1. This work provides a new insight into the effect of low dielectric constant additives on Zn2+ deposit for advanced aqueous zinc-ion batteries (AZIBs) development.
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