Copper ions-intercalated manganese dioxide self-supporting mesoporous carbon electrode for aqueous zinc-ion batteries

被引:2
|
作者
Jin, Richeng [1 ]
Fang, Yuan [1 ]
Gao, Beibei [1 ]
Wan, Ying [1 ]
Zhou, Yi [1 ]
Rui, Guofeng [1 ]
Sun, Wei [1 ]
Qiu, Pengpeng [1 ]
Luo, Wei [1 ]
机构
[1] Donghua Univ, Inst Funct Mat, Coll Mat Sci & Engn, State Key Lab Modificat Chem Fibers & Polymer Mat, Shanghai 201620, Peoples R China
来源
INDUSTRIAL CHEMISTRY & MATERIALS | 2025年 / 3卷 / 01期
基金
中国国家自然科学基金; 上海市自然科学基金;
关键词
NANOSPHERES; NANOSHEETS;
D O I
10.1039/d4im00042k
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
In aqueous zinc-ion batteries (AZIB), layered manganese dioxide (delta-MnO2) is considered to be a suitable cathode material due to its high theoretical capacity, suitable operating voltage and Zn2+/H+ co-intercalation mechanism. However, the strong coulomb interaction between Zn2+ and delta-MnO2 results in the slow diffusion dynamics of Zn2+ in the electrochemical process, which affects the structural stability of the cathode. Herein, we report a structural design that stabilizes the delta-MnO2-layered structure by pre-intercalation of Cu2+ to expand the layer spacing, and thus improve H+-transfer kinetics. Compared with the bulk delta-MnO2, the modified cathode showed excellent electrochemical performances, including a highly reversible capacity of 280 mA h g-1 at 1 A g-1 and 62.5% capacity retention after 1500 cycles at 5 A g-1. The results shown above confirmed the possibility of increasing the capacity contribution of H+ through structural design, and provides a novel idea for the development of high-performance cathode materials.Keywords: Aqueous zinc-ion batteries; Layered manganese dioxide; Pre-intercalation; Self-supporting electrode.
引用
收藏
页码:87 / 96
页数:10
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