阳极
锌
图层(电子)
金属
材料科学
离子
比例(比率)
无机化学
化学工程
纳米技术
化学
冶金
电极
工程类
有机化学
物理
物理化学
量子力学
作者
Kai Yang,Zhe Zhu,Xin He,Ruiqi Song,Xiaoqiao Liao,Leixin Wu,Yixue Duan,Chuan Zhao,Muhammad Tahir,Jun Dai,Hui Tang,Liang He
标识
DOI:10.1016/j.cej.2024.152114
摘要
Aqueous zinc (Zn) metal battery is regarded as a promising candidate with low cost and high safety for energy storage systems at large scales. However, the destabilized Zn2+ transport at the reaction interface severely restricts the lifespan of zinc anode, and the strategies suitable for large-scale integration of the anode's protection layer are required. Herein, an independent protective layer of Cu@CuO nanowire arrays is proposed to stabilize zinc anode with comprehensive regulation of Zn2+ transport. Through wet-chemical etching, the nanowire structure with a geometric area of 250 cm2 can be synthesized in one pot. From experimental analysis and simulation results, such a layer not only homogenizes the distribution of interfacial electric field, but also enhances Zn2+ transfer kinetics with improved ionic conductivity and increased transference number. Meanwhile, the activity of hydrogen evolution reaction (HER) is decreased due to the integration of this unique layer. As a result, the protected zinc anode can be stably operated at 2 mA cm−2/2 mAh cm−2, and the stable current density can further increase to 10 mA cm−2. Furthermore, the protective layer is featured with superior hydrophilicity, and can be feasibly utilized for large-area pouch cells, revealing the scalability and effectiveness in practical devices. This work proposes a facile protection strategy for zinc anode from the perspective of optimizing Zn2+ transport by large-scale integration of superior ion transport layer, showing great potential in high-performance zinc metal anode.
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