Shixue Zhong, Yan Xin*, Li’e Mo, Bijiao He, Fang Zhang, Chen Zhao, Linhua Hu* and Huajun Tian*,
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引用次数: 0
摘要
锰基层状化合物以其高安全性、低成本和环境友好性,为水相锌离子电池(AZIBs)正极材料提供了良好的应用前景。然而,它们的反应动力学缓慢,电导率差,以及不可逆的锰溶解导致严重的容量衰退。本文成功地提出了一种简单的两步法,将Ba2+离子插入到层状氧化锰(Ba-MnO2)中,并将其用作azib的正极材料。创新地将Ba2+离子引入MnO2阴极,产生丰富的氧空位。值得注意的是,加入的Ba2+在充电过程中自发形成原位BaSO4层,起到阴极电解质保护界面的作用。这些改进提高了MnO2的电导率和离子扩散,实现了MnO2/Mn2+可逆沉积/溶解反应。Zn//Ba-MnO2全电池在0.3℃下可提供355 mA h g-1的高容量,即使在3℃下也能保持超过1200次循环的超稳定循环稳定性。这项工作为azib高性能阴极的设计提供了创新的策略和深刻的理解。
Intercalation and Interface Engineering of Layered MnO2 Cathodes toward High-Performance Aqueous Zinc-Ion Batteries
Manganese-based layered compounds offer promising cathode materials for aqueous zinc-ion batteries (AZIBs) due to their high safety, low cost, and environmental friendliness. However, their sluggish reaction kinetics, poor conductivity, and irreversible manganese dissolution result in severe capacity fading. Herein, a simple two-step method is successfully proposed to intercalate Ba2+ ions into layered manganese oxide (Ba-MnO2), which were utilized as cathode materials for AZIBs. Ba2+ ions have been innovatively introduced into the MnO2 cathode, generating abundant oxygen vacancies. Notably, the incorporated Ba2+ spontaneously forms an in situ BaSO4 layer during charging, which functions as a protective cathode electrolyte interface. These improvements promote the conductivity and ion diffusion of MnO2, enabling a reversible MnO2/Mn2+ deposition/dissolution reaction. The Zn//Ba-MnO2 full battery delivers a high capacity of 355 mA h g–1 at 0.3 C and maintains an ultrastable cycling stability of over 1200 cycles even at 3 C. This work provides an innovative strategy and a profound understanding of designing high-performance cathodes for AZIBs.
期刊介绍:
The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.