An interfacial dual-regulation strategy for ultra-stable 3D Zn metal anodes

被引:0
|
作者
Liu, Chen [1 ,2 ,3 ]
Zeng, Jian [1 ]
Di, Shuanlong [4 ]
Wang, Shulan [4 ]
Li, Li [1 ,2 ,3 ]
机构
[1] Northeastern Univ, Sch Met, Shenyang 110819, Peoples R China
[2] Northeastern Univ, Foshan Grad Sch Innovat, Foshan 528311, Guangdong, Peoples R China
[3] Northeastern Univ, State Key Lab Rolling & Automat, Shenyang 110819, Liaoning, Peoples R China
[4] Northeastern Univ, Coll Sci, Dept Chem, Shenyang 110819, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
Zn metal anode; Array structure; 3D electrode; Long cycling lifespan; Homogeneous Zn deposition;
D O I
10.1016/j.actamat.2024.120433
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The development of Zn metal-batteries, which are viewed as one of the most potential alternatives to lithium ion batteries, is severely hindered by sluggish ion diffusion kinetics and uncontrollable dendritic growth for anodes. Herein, we propose an interfacial dual-regulation strategy for the fabrication of 3D Zn anode through the direct in-situ treatment of benchmark Zn foil. Both rapid ion migration dynamics and homogeneous bottom-up Zn2+ deposition are achieved due to the unique open nanoarray structure with superhydrophilic and zincophilic interface to the electrolyte. Theoretical calculations and finite element simulations reveal this design can effectively redistribute Zn2+ and increase ion flux with a long-lasting 3D diffusion mode, enabling exceptional reversibility during Zn plating/stripping. The as-prepared anode therefore achieves an ultralong lifespan over 3000 h along with high rate capability even at 40 mA cm(-2) (depth of discharge approximate to 68.4%). Furthermore, its practical feasibility is validated by a superior capacity retention of 92.5% after 1000 cycles for full cell and high capacity of 112.2 mAh g(-1) for pouch cell. This study opens up new opportunities for the development of dendrite-free anodes for aqueous metal batteries.
引用
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页数:9
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