锌
材料科学
动力学
离子
无机化学
冶金
化学
有机化学
物理
量子力学
作者
Yunting Yang,Zhoujie Tang,Shuyang Bian,Yalan Gu,Fei Ye,Wenshu Chen,Kongjun Zhu,Yuping Wu,Linfeng Hu
标识
DOI:10.1002/aenm.202500316
摘要
Abstract Rechargeable zinc‐ion batteries (ZIBs) have gained significant attention as potential next‐generation energy storage systems, owing to their inherent safety, environmental benignity, and cost‐effectiveness. However, the substantial electrostatic repulsion of Zn ion results in a sluggish kinetics for its insertion into the cathode material. Meanwhile, the formation of hydrated ionic groups with increased mass and volume in the aqueous electrolyte further hampers the transport ability of zinc ions, significantly impacting the overall electrochemical performance (including capacity, energy density, rate‐capability, and cyclability) of aqueous zinc‐ion batteries. This review systematically summarized the recent progress in the regulation strategy of the zinc‐ion transport kinetics. The as‐reported mechanisms are introduced for zinc ion transport in ZIBs (Zn 2+ insertion/extraction mechanism, H + or H 2 O/ Zn 2+ co‐insertion/extraction mechanism, conversion reaction mechanism, and coordination reaction mechanism). Then, cathode material design for fast zinc‐ion transport kinetics including soft lattice construction, doping effects, defect introduction, morphology control, and interface design is systematically summarized. Finally, it is concluded with future research directions, such as high‐entropy design, multi‐scale simulation, and machine study, providing a roadmap for developing high‐performance zinc ion batteries at ultralow operation temperatures.
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