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水系锌-β-二氧化锰二次电池的运行机制

Functioning Mechanism of the Secondary Aqueous Zn-β-MnO Battery.

作者信息

Li Longyan, Hoang Tuan K A, Zhi Jian, Han Mei, Li Shengkai, Chen P

机构信息

School of Chemistry and Materials Science, Nanjing University of Information Science and Technology, Nanjing 210044, China.

Department of Chemical Engineering and Waterloo Institute of Nanotechnology, University of Waterloo, Waterloo, Ontario N2L 3G1, Canada.

出版信息

ACS Appl Mater Interfaces. 2020 Mar 18;12(11):12834-12846. doi: 10.1021/acsami.9b22758. Epub 2020 Mar 5.

Abstract

Rechargeable aqueous Zn-MnO batteries are a promising candidate for large-scale energy storage systems due to their outstanding advantages, such as high energy density, high safety, low cost, and environmental friendliness. Considering the controversies surrounding the mechanism of this battery containing a mildly acidic electrolyte, the electrochemical behavior of this type of battery using β-MnO as the cathode is systematically investigated. The results indicate that the reversible intercalation of Zn ions into MnO is not likely to take place in the aqueous system. We conclude that it is the existence of the water molecule and its participation in the electrochemical reactions, for instance, the reversible insertion of proton into MnO and the electrolysis of water, that makes the mechanism of aqueous Zn-MnO batteries complicated. Besides, the capacity fading of this mildly acidic Zn-MnO battery is assigned to the generation of the inert layer of ZnSO(OH)·HO and the ZnMnO on the cathode via electrochemical conversion reactions, the dissolution of the active material during discharging, and the release of gases. When Mn ions are available in the electrolyte, they will be electrodeposited on the cathode during charging, and the kinetics of the electrochemical reactions of the electrode is improved, leading to the higher electrochemical performance of the battery.

摘要

可充电水系锌-二氧化锰电池因其具有高能量密度、高安全性、低成本和环境友好等突出优点,是大规模储能系统的一个有前景的候选者。考虑到围绕这种含微酸性电解质的电池机理存在的争议,系统地研究了以β-二氧化锰为正极的这类电池的电化学行为。结果表明,在水系体系中锌离子不太可能可逆地嵌入二氧化锰中。我们得出结论,是水分子的存在及其参与电化学反应,例如质子可逆地插入二氧化锰和水的电解,使得水系锌-二氧化锰电池的机理变得复杂。此外,这种微酸性锌-二氧化锰电池的容量衰减归因于通过电化学转化反应在正极上生成ZnSO(OH)·H₂O和ZnMnO的惰性层、放电过程中活性材料的溶解以及气体的释放。当电解质中有锰离子时,它们会在充电过程中电沉积在正极上,并且电极电化学反应的动力学得到改善,从而导致电池具有更高的电化学性能。

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