Electrodeposited Zinc-Based Films as Anodes for Aqueous Zinc Batteries

阳极 材料科学 电偶阳极 箔法 合金 电化学 电解质 冶金 黄铜 极化(电化学) 电池(电) 电极 法拉第效率 阴极 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 Jung Chang,Ismael A. Rodríguez‐Pérez,David M. Reed
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:12 (38): 42763-42772 被引量:55
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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