Nature-inspired interfacial engineering for highly stable Zn metal anodes

被引:36
作者
Deng, Canbin [1 ,2 ,3 ]
Li, Yang [4 ]
Liu, Sijing [4 ]
Yang, Jinglei [4 ]
Huang, Baoling [4 ]
Liu, Jiapeng [5 ]
Huang, Jiaqiang [1 ,2 ,3 ]
机构
[1] Hong Kong Univ Sci & Technol Guangzhou, Sustainable Energy & Environm Thrust, Guangzhou 511400, Guangdong, Peoples R China
[2] Hong Kong Univ Sci & Technol, Interdisciplinary Programs Off, Clear Water Bay, Hong Kong, Peoples R China
[3] HKUST Shenzhen Hong Kong Collaborat Innovat Res In, Shenzhen 518045, Guangdong, Peoples R China
[4] Hong Kong Univ Sci & Technol, Dept Mech & Aerosp Engn, Clear Water Bay, Hong Kong, Peoples R China
[5] AI Sci Inst, Beijing 100080, Peoples R China
基金
中国国家自然科学基金;
关键词
Battery biomimicry; Zn metal anodes; Interfacial engineering; Humic acid; Chelation; Desolvation; HUMIC-ACID; PERFORMANCE; DESOLVATION; DEPOSITION; DESIGN;
D O I
10.1016/j.ensm.2023.03.028
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 zinc-ion batteries (ZIBs) emerge as a potential candidate for large-scale energy storage applications, due to their low cost, eco-friendliness, and high safety. However, nowadays, ZIBs still suffer from poor cycling sta-bility, owing largely to the severe dendrite growth, corrosion, and hydrogen evolution at the electrolyte/anode interface. Herein, inspired by the biomolecule-assisted cationic transport mechanism in nature, we apply humic acid (HA, a natural ingredient of soil) on the Zn surface for stabilizing the anode/electrolyte interface. Density functional theory calculations indicate that the tuned interactions between Zn2+ and the segments of HA possibly facilitate the desolvation of Zn2+. The theoretical results are supported by the electrochemical analyses, where the HA-induced interfacial layer promotes the reversible Zn deposition kinetics and suppresses the corrosion and hydrogen evolution. The improved electrochemical performance is validated by Zn/MnO2 coin and pouch cells. These findings not only provide insights into engineering electrolyte/electrode interfaces but also suggest that a broader family of materials, structures, and mechanisms in nature can be leveraged for more sustainable batteries.
引用
收藏
页码:279 / 286
页数:8
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