材料科学
过电位
锌
阳极
纤锌矿晶体结构
化学工程
电导率
兴奋剂
枝晶(数学)
离子
储能
无机化学
电镀(地质)
光电子学
冶金
电化学
物理化学
电极
有机化学
化学
物理
地质学
工程类
量子力学
功率(物理)
数学
地球物理学
几何学
作者
Siwei Zhao,Yujing Zhang,Jidao Li,Limin Qi,Yuxin Tang,Jia Zhu,Jian Zhi,Fuqiang Huang
标识
DOI:10.1002/adma.202300195
摘要
Although zinc-based batteries are promising candidates for eco-friendly and cost-effective energy storage devices, their performance is severely retarded by dendrite formation. As the simplest zinc compounds, zinc chalcogenides, and halides are individually applied as a Zn protection layer due to high zinc ion conductivity. However, the mixed-anion compounds are not studied, which constrains the Zn2+ diffusion in single-anion lattices to their own limits. A heteroanionic zinc ion conductor (Zny O1-x Fx ) coating layer is designed by in situ growth method with tunable F content and thickness. Strengthened by F aliovalent doping, the Zn2+ conductivity is enhanced within the wurtzite motif for rapid lattice Zn migration. Zny O1-x Fx also affords zincophilic sites for oriented superficial Zn plating to suppress dendrite growth. Therefore, Zny O1-x Fx -coated anode exhibits a low overpotential of 20.4 mV for 1000 h cycle life at a plating capacity of 1.0 mA h cm-2 during symmetrical cell test. The MnO2 //Zn full battery further proves high stability of 169.7 mA h g-1 for 1000 cycles. This work may enlighten the mixed-anion tuning for high-performance Zn-based energy storage devices.
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