Enhanced cycling stability achieved by the nitrogen doped carbon coating layer for electrodeposited Mn3O4 in aqueous zinc ion batteries

被引:22
|
作者
Zhou, Zixiang [1 ]
Liu, Shuling [1 ]
Wang, Jie [1 ]
Wu, Yili [1 ]
Yang, Yifan [1 ]
Li, Yvpei [1 ]
Wang, Jinlian [1 ]
Wang, Chao [1 ]
机构
[1] Shaanxi Univ Sci & Technol, Youth Innovat Team Shaanxi Univ, Shaanxi Collaborat Innovat Ctr Ind Auxiliary Chem, Dept Chem & Chem Engn,Key Lab Auxiliary Chem & Tec, Xian 710021, Shaanxi, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Zn-ion batteries; N-doped carbon; Capacity; Electrochemical performance; MANGANESE-DIOXIDE; CATHODE MATERIAL; PERFORMANCE; MECHANISMS; NANORODS; HYBRID; GROWTH;
D O I
10.1016/j.apsusc.2022.156259
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
Aqueous rechargeable Zn-ion batteries (ZIBs) are promising candidates for large scale energy storage. Unfortu-nately, their application is hindered by the quick capacity fading. Herein, the Mn3O4@N-doped carbon coated carbon cloth electrodes (Mn3O4@NC/CC) are prepared by electrodeposition and calcination and are used as the cathode for ZIBs. The thickness of the electrodeposited Mn3O4 is -200 nm, and the NC layer is -10 nm. The ZIB with Mn3O4@NC/CC displays the capacity of 265.8 mAh g-1 at 0.2 A g-1, and has a high reversible capacity of 165.6 mAh g-1 after 2000 charged -discharged cycles at 3 A g-1. The capacitive-controlled processes contribute mainly to the charge storage mechanism. The introduction of NC layer can effectively prevent the disintegration of active material during charge-discharge cycling. The NC layer can also hinder the diffusion of Zn2+ and enhance Rct, that leads to suppressed Zn ion insertion/extraction and possibly milder change in crystal structure. Ex-situ characterization shows that the Mn3O4 is irreversibly converted to R-MnO2 after multiple charge -discharge cycles, and both H+ and Zn2+ participate in the charge storage processes.
引用
收藏
页数:9
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