成核
材料科学
阳极
电偶阳极
锌
化学工程
水溶液
微尺度化学
电化学
涂层
耐久性
枝晶(数学)
电偶腐蚀
腐蚀
纳米技术
冶金
复合材料
电极
化学
有机化学
物理化学
工程类
数学教育
数学
几何学
阴极保护
作者
Xin Liu,Jia‐Wei Qian,Jingwei Chen,Yunkai Xu,Weiyi Wang,Wei‐Xu Dong,Wei Hu,Guorui Cai,Jun Lü,Shu‐Hong Yu,Lifeng Chen
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-03-25
卷期号:64 (26): e202504613-e202504613
被引量:38
标识
DOI:10.1002/anie.202504613
摘要
Abstract Aqueous zinc metal batteries are promising candidates for large‐grid energy storage due to their safety, cost‐effectiveness, and durability. However, challenges like dendrite growth, corrosion, and the hydrogen evolution reaction (HER) on the zinc anode hinder their performance. Herein, we propose a sustainable and scalable approach to form a copper gluconate@carboxymethyl chitosan@kaolin (CuCK) interface layer, inducing gradient nucleation sites via in situ galvanic and galvanostatic processes. The biomass‐based CuCK coating features a gradient Cu x Zn y alloy structure that homogenizes interfacial electric field distribution and enhances electrochemical stability. Furthermore, the incorporated Cu 2+ ‐loaded kaolin and carboxymethyl chitosan regulate Zn 2+ flux, accelerate Zn 2+ desolvation, and suppress HER. The resulting Zn@CuCK anode achieves a high cumulative capacity of 5500 mAh cm −2 in symmetrical cells, exhibits excellent durability in Zn@CuCK//NaV 3 O 8 ·1.5H 2 O full cells across a wide temperature range (−30 to 60 °C), and endows the assembly of pouch cells with high energy density.
科研通智能强力驱动
Strongly Powered by AbleSci AI