电解质
锡
阳极
电镀(地质)
腐蚀
氯化物
水溶液
电池(电)
硫酸
阴极
金属
材料科学
无机化学
电极
钝化
化学
化学工程
冶金
纳米技术
有机化学
物理化学
功率(物理)
物理
量子力学
图层(电子)
地球物理学
工程类
地质学
作者
Songyang Chang,Wentao Hou,Angelica Del Valle-Perez,Irfan Ullah,Qiu Shen,Jeileen Luciano Rodriguez,Liz M. Díaz-Vázquez,Lisandro Cunci,Gerardo Morell,Xianyong Wu
出处
期刊:Angewandte Chemie
[Wiley]
日期:2024-09-20
卷期号:64 (2): e202414346-e202414346
被引量:22
标识
DOI:10.1002/anie.202414346
摘要
Tin (Sn) metal has emerged as a promising anode for aqueous batteries, due to its high capacity, non-toxicity, and cost-effectiveness. However, Sn metal has often been coupled with strong and corrosive sulfuric acids (2-3 M), leading to severe electrode corrosion and hydrogen evolution issues. Although high efficiency and long cycling were reported, the results were achieved using high currents to kinetically mask electrode-electrolyte side reactions. Herein, we introduce a low-acidity tin chloride electrolyte (pH=1.09) as a more viable option, which eliminates the need of strong acids and enables a reversible dendrite-free Sn plating chemistry. Remarkably, the plating efficiency approaches unity (99.97 %) under standard testing conditions (1 mA cm-2 for 1 mAh cm-2), which maintains high at 99.23-99.93 % across various aggressive conditions, including low current (0.1-0.25 mA cm-2), high capacity (5-10 mAh cm-2), and extended resting time (24-72 hours). The battery calendar life is further prolonged to 3064 hours, significantly surpassing literature reports. Additionally, we presented an effective method to mitigate the potential Sn2+ oxidization issue on the cathode, demonstrating long-cycling Sn||LiMn2O4 hybrid batteries. This work offers critical insights for developing highly reversible Sn metal batteries.
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