SusMat | |
Recent progress, mechanisms, and perspectives for crystal and interface chemistry applying to the Zn metal anodes in aqueous zinc‐ion batteries | |
Jinkui Feng1  Weihua Chen2  Xiaojian Ma3  Shenglin Xiong3  Baojuan Xi3  Zhengchunyu Zhang3  | |
[1] Key Laboratory for Liquid−Solid Structural Evolution & Processing of Materials Ministry of Education School of Materials Science and Engineering Shandong University Jinan P.R. China;Key Laboratory of Material Processing and Mold of Ministry of Education Zhengzhou University Zhengzhou P.R. China;School of Chemistry and Chemical Engineering State Key Laboratory of Crystal Materials Shandong University Jinan P.R. China; | |
关键词: crystal chemistry; interface chemistry; side reaction; Zn dendrites; Zn metal anode; | |
DOI : 10.1002/sus2.53 | |
来源: DOAJ |
【 摘 要 】
Abstract The need for large‐scale electrochemical energy storage devices in the future has spawned several new breeds of batteries in which aqueous zinc ion batteries (AZIBs) have attracted great attention due to their high safety, low cost, and excellent electrochemical performance. In the current research, the dendrite and corrosion caused by aqueous electrolytes are the main problems being studied. However, the research on the zinc metal anode is still in its infancy. We think it really needs to provide clear guidelines about how to reasonably configure the system of AZIBs to realize high‐energy density and long cycle life. Therefore, it is worth analyzing the works on the zinc anode, and several strategies are proposed to improve the stability and cycle life of the battery in recent years. Based on the crystal chemistry and interface chemistry, this review reveals the key factors and essential causes that inhibit dendrite growth and side reactions and puts forward the potential prospects for future work in this direction. It is foreseeable that guiding the construction of AZIBs with high‐energy density and long cycle life in various systems would be quite possible by following this overview as a roadmap.
【 授权许可】
Unknown