电解质
钝化
锌
过电位
无机化学
电化学
水溶液
阳极
电偶阳极
材料科学
电化学电位
螯合作用
化学
化学工程
电极
阴极保护
纳米技术
冶金
有机化学
物理化学
图层(电子)
工程类
作者
Yuting Xia,Rong‐Ao Tong,Jingxi Zhang,Mingjie Xu,Gang Shao,Hailong Wang,Yanhao Dong,Chang‐An Wang
标识
DOI:10.1007/s40820-023-01305-0
摘要
Abstract Aqueous zinc-ion batteries are promising due to inherent safety, low cost, low toxicity, and high volumetric capacity. However, issues of dendrites and side reactions between zinc metal anode and the electrolyte need to be solved for extended storage and cycle life. Here, we proposed that an electrolyte additive with an intermediate chelation strength of zinc ion—strong enough to exclude water molecules from the zinc metal-electrolyte interface and not too strong to cause a significant energy barrier for zinc ion dissociation—can benefit the electrochemical stability by suppressing hydrogen evolution reaction, overpotential growth, and dendrite formation. Penta-sodium diethylene-triaminepentaacetic acid salt was selected for such a purpose. It has a suitable chelating ability in aqueous solutions to adjust solvation sheath and can be readily polarized under electrical loading conditions to further improve the passivation. Zn||Zn symmetric cells can be stably operated over 3500 h at 1 mA cm −2 . Zn||NH 4 V 4 O 10 full cells with the additive show great cycling stability with 84.6% capacity retention after 500 cycles at 1 A g −1 . Since the additive not only reduces H 2 evolution and corrosion but also modifies Zn 2+ diffusion and deposition, highlyreversible Zn electrodes can be achieved as verified by the experimental results. Our work offers a practical approach to the logical design of reliable electrolytes for high-performance aqueous batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI