阳极
锌
材料科学
电偶阳极
箔法
合金
化学工程
电化学
电解质
锰
冶金
黄铜
极化(电化学)
电池(电)
铜
电极
腐蚀
法拉第效率
涂层
阴极
纳米棒
阴极保护
复合材料
化学
功率(物理)
物理化学
物理
量子力学
作者
Matthew Fayette,Hee Jin Chang,Ismael A. Rodríguez-Pérez,Xin Li,David Reed
标识
DOI:10.1021/acsami.0c10956
摘要
Zinc-based batteries have attracted extensive attention in recent years, due to high safety, high capacities, environmental friendliness, and low cost compared to lithium-ion batteries. However, the zinc anode suffers primarily from dendrite formation as a mode of failure in the mildly acidic system. Herein, we report on electrochemically deposited zinc (ED Zn) and copper-zinc (brass) alloy anodes, which are critically compared with a standard commercial zinc foil. The film electrodes are of commercially relevant thicknesses (21 and 25 μM). The electrodeposited zinc-based anodes exhibit low electrode polarization (∼0.025 V) and stable cycling performance in 50 cycle consecutive experiments from 0.26 to 10 mA cm-2 compared to commercial Zn foil. Coulombic efficiencies at 1 mA cm-2 were over 98% for the electrodeposited zinc-based materials and were maintained for over 100 cycles. Furthermore, full cells with an electrodeposited Zn/brass anode, electrolytic manganese dioxide (EMD) cathode, in 1 M ZnSO4 + 0.1 M MnSO4 delivered capacities of 96.3 and 163 mAh g-1, respectively, at 100 mA g-1 compared to 92.1 mAh g-1 for commercial Zn. The electrodeposited zinc-based anodes also show better rate capability, delivering full cell capacities of 35.9 and 47.5 mAh g-1 at a high current of up to 3 A g-1. Lastly, the electrodeposited zinc-based anodes show enhanced capacity for up to 100 cycles at 100 mA g-1, making them viable anodes for commercial use.
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