Microfluidic-oriented assembly of Mn3O4@C/GFF cathode with multiscale synergistic structure for high-performance aqueous zinc-ion batteries

被引:13
|
作者
Li, Chang [1 ,2 ]
Hu, Chaoquan [1 ,2 ]
Song, Yang [1 ,2 ]
Gao, Ning [1 ]
Yang, Weisheng [3 ]
Xu, Xuebing [1 ,2 ]
机构
[1] Nanjing IPE Inst Green Mfg Ind, Nanjing 211135, Jiangsu, Peoples R China
[2] Inst Proc Engn, Chinese Acad Sci, State Key Lab Multiphase Complex Syst, Beijing 100190, Peoples R China
[3] Nanjing Forestry Univ, Coll Mat Sci & Engn, Nanjing 210037, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Zinc -ion battery; Microfluidic assembly; Freestanding cathode; Multiscale synergistic; Long-term stability; OXIDE; MNO2; CAPABILITY; MN3O4;
D O I
10.1016/j.carbon.2023.03.058
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
The electrochemical activity and long-term stability of cathodic materials, as well as active ion transport, are key factors for efficient energy storage in aqueous zinc-ion batteries (ZIBs). Here, a freestanding Mn3O4@C nanowireimplanted graphene-based fiber fabric (Mn3O4@C/GFF) cathode with a multiscale synergistic structure was fabricated using a facile microfluidic assembly method. In this architecture, Mn3O4 nanowires are hosted by a conductive carbon layer and then anchored in the interlayer of a self-assembled graphene-based fiber framework. The hierarchical structure enhances electrical conductivity and relieves ion leaching, thereby boosting the electrochemical activity and long-term stability of cathodic materials. Furthermore, the layer-by-layer assembled structure of the Mn3O4@C/GFF cathode provides ample available channels for active ion transport, accelerating the electrochemical kinetics. Consequently, the Mn3O4@C/GFF cathode exhibits enhanced electrochemical performance with a high capacity of 374.8 mAh g-1 at 0.2 A g-1 and ultralong cycle life (158.7 mAh g-1 retained over 5000 cycles at 2 A g-1). Therefore, this study provides a multiscale synergistic strategy for fabricating advanced cathodes for high-performance ZIBs.
引用
收藏
页码:247 / 254
页数:8
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