电解质
阳极
电池(电)
钝化
锌
法拉第效率
材料科学
成核
电偶阳极
水溶液
化学工程
纳米技术
化学
图层(电子)
冶金
工程类
电极
物理
物理化学
阴极保护
有机化学
功率(物理)
量子力学
作者
Yang Li,Xiaoxu Liu,Man Zhang,Dawei Sheng,Peipei Ren,Lida Che,Xiaofeng Wang,Zexiang Shen
出处
期刊:ACS materials letters
[American Chemical Society]
日期:2024-04-12
卷期号:6 (5): 1938-1960
被引量:7
标识
DOI:10.1021/acsmaterialslett.4c00308
摘要
Aqueous zinc-ion batteries (AZIBs) are increasingly regarded as promising candidates for large-scale energy storage, because of their advantageous features such as high safety, low cost, abundant resources, and environmental friendliness. However, challenges persist with zinc anodes, including issues such as low Coulombic efficiency (CE) and poor long-term cycle stability due to zinc dendrites, hydrogen evolution, and passivation reactions. These challenges are mainly attributed to the thermodynamic instability of zinc anodes in aqueous electrolytes, leading to a shorter battery cycle life. The optimization of the electrolyte structure has emerged as a straightforward and impactful strategy, making substantial advancements in addressing issues associated with zinc anodes in a systematic manner. This account undertakes a comprehensive analysis of the formation process of the interface structure between the electrolyte and the zinc anode. Strategies for optimization involve precise regulation of the Zn nucleation layer, the construction of in situ artificial anode interface optimization, and the design of the solid electrolyte interphase (SEI) protective layer. By delving into these critical aspects, the review aims to provide a concise synthesis and future outlook on electrolyte interface structure design strategies for aqueous zinc-ion batteries, offering valuable insights for enhancing overall battery performance.
科研通智能强力驱动
Strongly Powered by AbleSci AI