Stabilizing zinc anodes by a solvation sheath modification with toluenesulfonate additive

被引:6
作者
Liu, Hengshuo [1 ]
Zhang, Dongdong [1 ,2 ]
Chanajaree, Rungroj [3 ]
Wu, Xiang [1 ]
Zhang, Xinyu [2 ]
Qin, Jiaqian [3 ]
Cao, Jin [4 ]
机构
[1] Shenyang Univ Technol, Sch Mat Sci & Engn, Shenyang 110870, Peoples R China
[2] Yanshan Univ, State Key Lab Metastable Mat Sci & Technol, Qinhuangdao 066004, Peoples R China
[3] Chulalongkorn Univ, Met & Mat Sci Res Inst, Bangkok 10330, Thailand
[4] China Three Gorges Univ, Coll Mat & Chem Engn, Yichang 443002, Hubei, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Aqueous zinc-ion batteries; Side reactions; Dendrite-free; Additives; Solvation structure; PERFORMANCE;
D O I
10.1016/j.jpowsour.2024.235667
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
As an advanced electrochemical energy storage device, aqueous zinc-ion batteries offer high theoretical capacity and energy density, employing water-based electrolytes to reduce fire and explosion risks. However, zinc tends to form dendrites during charge-discharge processes, leading to reduced electrode surface area and shortened cycling lifespan. In this study, we propose the use of a commonly used and cost-effective additive, sodium ptoluenesulfonate (OTM), to stabilize zinc anodes. Experimental and theoretical simulations demonstrate that OTM can enter the solvation sheath of Zn2+, reduce the activity of nearby H2O molecules, facilitate uniform Zn2+ deposition, and suppress zinc dendrite formation. Therefore, Zn//Zn symmetric batteries utilizing ZnSO4 (ZSO) electrolytes containing OTM achieved outstanding long-term performance exceeding 1700 h at 1 mA cm- 2 , significantly surpassing those employing ZSO electrolytes. Additionally, Zn//VO2 full batteries with OTM additives exhibited enhanced cycling stability and an initial discharge capacity of 180 mAh g- 1 at 3 A g- 1 , demonstrating its superior application potential.
引用
收藏
页数:7
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