阳极
材料科学
法拉第效率
阴极
化学工程
水溶液
枝晶(数学)
同种类的
金属
电偶阳极
纳米技术
电极
冶金
阴极保护
物理化学
化学
热力学
工程类
物理
几何学
数学
作者
Chengwu Yang,Pattaraporn Woottapanit,Sining Geng,Kittima Lolupiman,Qian Zhang,Zhiyuan Zeng,Guanjie He,Jiaqian Qin
标识
DOI:10.1002/adma.202408908
摘要
Abstract The practical implementation of aqueous Zn‐ion batteries presents formidable hurdles, including uncontrolled dendrite growth, water‐induced side reactions, suboptimal Zn metal utilization, and intricate Zn anode manufacturing. Here, large‐scale construction of a highly oriented ZnO(002) lattice plane on Zn anode (ZnO(002)@Zn) with thermodynamic inertia and kinetic zincophilicity is designed to address such problems. Both theoretical calculations and experiment results elucidate that the ZnO(002)@Zn possesses high Zn chemical affinity, hydrogen evolution reaction suppression, and dendrite‐free deposition ability due to the abundant lattice oxygen species in ZnO(002) and its low lattice mismatch with Zn(002). These features synergistically promote ion transport and enable homogeneous Zn deposition. Consequently, the ZnO(002)@Zn anode displays a stable and prolonged cycling lifespan exceeding 500 h even under a larger depth of discharge (85.6%) and realizes an impressive average Coulombic efficiency of 99.7%. Moreover, its efficacy is also evident in V 2 O 5 ‐cathode coin cells and pouch cells with not only high discharge capacity but also exceptional cycling stability. This integrated approach presents a promising avenue for addressing the challenges associated with Zn metal anodes, thereby advancing the prospects of aqueous Zn‐ion battery technologies.
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