阴极
材料科学
纳米技术
普鲁士蓝
储能
涂层
电池(电)
纳米结构
水溶液
重量分析
高能
表征(材料科学)
金属有机骨架
电化学
能量密度
电镀
插层(化学)
工艺工程
纳米材料
表面能
作者
Yuewen Gong,Miao Jia,Qiong Yuan,Biao Yang
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2025-10-21
卷期号:30 (20): 4143-4143
被引量:8
标识
DOI:10.3390/molecules30204143
摘要
Owing to the inherent safety, environmental friendliness, and high theoretical capacity (820 mAh g−1) of zinc metal, aqueous zinc-ion batteries (AZIBs) have emerged as up-and-coming alternatives to organic lithium-ion batteries. However, the insufficient electrochemically active sites, poor structural stability, and severe interfacial side reactions of cathode materials have always been key challenges, restricting battery gravimetric energy density and cycling stability. This article systematically reviews current mainstream AZIB cathode material systems, encompassing layered manganese- and vanadium-based metal oxides, Prussian blue analogs, and emerging organic polymers. It focuses on analyzing the energy storage mechanisms of different material systems and their structural evolution during Zn2+ (de)intercalation. Furthermore, mechanisms of innovative strategies for improving cathodes are thoroughly examined here, such as nanostructure engineering, lattice doping control, and surface coating modification, to address common issues like structural degradation, manganese/vanadium dissolution, and interface passivation. Finally, this article proposes future research directions: utilizing multi-scale in situ characterization to elucidate actual reaction pathways, constructing artificial interface layers to suppress side reactions, and optimizing full-cell design. This review provides a new perspective for developing practical AZIBs with high specific energy and long lifespans.
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