Design principles of underpotential deposition chemistry for highly reversible multivalent metal anodes

被引:0
|
作者
Zhang, Yu [1 ]
Ge, Yanzeng [1 ]
Xu, Hengyue [2 ]
Tang, Si [1 ]
Li, Jing [1 ]
Zhang, Hui [1 ]
Tian, Xinlong [1 ]
Yang, Jinlin [1 ]
机构
[1] Hainan Univ, Sch Marine Sci & Engn, Sch Chem & Chem Engn, Haikou 570228, Peoples R China
[2] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
基金
中国国家自然科学基金;
关键词
Multivalent metal batteries; Aqueous batteries; Underpotential deposition; Heterointerface; CHALLENGES;
D O I
10.1016/j.ensm.2024.103991
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 multivalent metal batteries have high theoretical capacities and are cost-effective; however, the low electrochemical reversibility caused by the notorious parasitic reactions of metal anodes hinders their practical application. In this study, an underpotential deposition (UPD) strategy for designing heterogeneous metal substrates to regulate the multivalent metal plating/stripping behavior was developed. Using Al as a model system, a theory-to-application metric to screen proper heterogeneous metal was established through the theoretical and experimental evaluation of eight common metals according to their thermodynamics stability and kinetics aluminophilicity. Specifically, Sn metal has a strong binding affinity for Al3+ ions and can effectively alleviate the hydrogen evolution reaction, thus enabling highly reversible underpotential Al plating/stripping for over 2800 h at 1 mA cm-2, considerably longer than that of Al metal. Furthermore, the UPD strategy could be extended to other multivalent metals, including divalent Mg and Sn and trivalent In. This study provided an effective strategy for improving the reversibility of metal plating/stripping and constructing high-stability multivalent metal batteries.
引用
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页数:9
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