Electrochemical one-step synthesis of Mn3O4 with tunable oxygen defects for high-performance aqueous zinc-ion batteries

被引:14
作者
He, Yuling [1 ]
Pu, Yi [1 ]
Zhu, Bin [1 ]
Zhu, Haijiang [1 ]
Wang, Chao [2 ]
Tang, Wu [1 ]
Tang, Hui [1 ]
机构
[1] Univ Elect Sci & Technol China, Sch Mat & Energy, Chengdu 611731, Peoples R China
[2] China Acad Engn Phys, Inst Machinery Mfg Technol, Mianyang 621900, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
Aqueous Zinc -ion batteries; Electrochemical corrosion; Oxygen defects; Manganese oxides; ENERGY-STORAGE; CATHODE; COMPOSITE; OXIDES;
D O I
10.1016/j.jallcom.2022.167933
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Manganese-based oxides have been widely studied as promising aqueous zinc-ion battery cathodes. However, the development of manganese oxides still faces great challenges due to rapid capacity decline and sluggish reaction kinetics. Oxygen-defect manganese oxides cathodes can improve electrochemical activity and inherent stability by changing the bulk electronic structure and the surface properties. In this work, oxygen-defect Mn3O4 nanosheets were synthesized by a facile electrochemical corrosion method, and the concentrations of oxygen vacancies were controlled by adjusting alternating current (AC) and direct current (DC) superimposed power supply. The oxygen vacancy concentration impacted the electrochemical performance of the Mn3O4 cathodes. The aqueous zinc-ion battery with Mn3O4 cathode with the optimal oxygen vacancy concentration exhibited a high specific capacity (456 mA h g-1 at 0.1 A g-1) and long-cycle stability with high reversible capacity (94 % retained after 2000 cycles at 1.0 A g-1). Furthermore, the conversion mechanism with complex phase transformations was explored by ex-situ characterization after the charge/discharge cycling, indicating the co-insertion of H+ and Zn2+ in the Mn3O4 electrode.(c) 2022 Elsevier B.V. All rights reserved.
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页数:9
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