法拉第效率
过电位
阳极
水溶液
储能
化学工程
材料科学
电偶阳极
涂层
锌
电池(电)
无机化学
电化学
表面工程
离子
离子键合
基础(拓扑)
金属
电化学储能
螯合作用
过渡金属
水溶液中的金属离子
金属有机骨架
母材
锂离子电池的纳米结构
枝晶(数学)
电镀(地质)
纳米技术
化学
表面改性
催化作用
电化学能量转换
作者
Xiaoqian Xu,Kang Xu,Yuting Qin,Jiahui Lu,Tianyi Wang,Chengyin Wang
出处
期刊:Chemsuschem
[Wiley]
日期:2025-11-24
卷期号:19 (1): e202502123-e202502123
被引量:1
标识
DOI:10.1002/cssc.202502123
摘要
Aqueous zinc‐ion batteries are attractive for large‐scale energy storage but are limited by dendrite growth and side reactions at the Zn anode. In this work, we design a functional coating strategy using Zn–Schiff base complexes to overcome these issues. The complexes, featuring abundant coordination sites and ionic conductivity, modulate Zn 2+ transport and promote desolvation, ensuring uniform deposition. Three complexes—Zn–salen, Zn–salpn, and Zn–salbn—were developed, among which Zn–salbn exhibited the best performance. Symmetric Zn||Zn cells with Zn–salbn@Zn anodes cycled stably for 2310 h at 1 mA cm −2 /1 mAh cm −2 with a low overpotential of 31.9 mV, while delivering a high average Coulombic efficiency of 99.7%. In full cells, pairing Zn–salbn@Zn with V 2 O 5 enabled 83.1% capacity retention after 1000 cycles at 0.5 A g −1 . This work not only demonstrates the effective protection of Zn metal anodes by Schiff base complexes, but also provides new insights into the application of interfacial chelation strategies in next generation high performance energy storage technologies.
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