锌
水溶液
多孔性
阳极
原位
组分(热力学)
图层(电子)
材料科学
离子
电偶阳极
化学工程
无机化学
化学
电极
冶金
纳米技术
有机化学
复合材料
工程类
阴极保护
物理化学
物理
热力学
作者
Qiuyang Luo,Shu Xia,Junnan Liu,Xingfu Yang,Jie Lei,Yan Shi,Xiaohu Chen,Jiao‐Jing Shao,Tang Xiaoning,Guangmin Zhou
标识
DOI:10.1016/j.cej.2024.152789
摘要
Aqueous zinc ion batteries (AZIBs) with Zn metal anodes stand out as a promising candidate for large-scale energy storage systems, owing to their high safety, low cost, and environmental friendliness. However, the commercialization of AZIBs is plagued by issues such as Zn dendrite growth and side reactions. Herein, an organic component-Cu metal composite layer is constructed on Zn anode (Org-Cu@Zn) by a novel, one-step and in situ spontaneous displacement reaction. The outer porous organic layer with functional groups may serve as migration sites and transport channels for Zn2+ ions, promoting transfer kinetics. The inner zincophilic Cu clusters layer diminishes the interfacial resistance, facilitating Zn2+ ions diffusion and even Zn deposition. Compared to the bare Zn, the unique dual-layer structure exhibits stronger zincophilicity, smaller interface resistance, lower nucleation energy barrier, and stronger anti-corrosion capability, thus effectively suppressing the Zn dendrite growth and side reactions. Remarkably, the Org-Cu@Zn electrode shows an ultra-long lifespan of 3600 h (1800 cycles) with an average Coulombic efficiency of 99.7 %, realizes long cycling stability over 4300 h (1 mA cm−2) and 1350 h (5 mA cm−2), and assures the stable operation of Org-Cu@Zn||ZVO full cells with coin-type configurations.
科研通智能强力驱动
Strongly Powered by AbleSci AI