Dendrite-Free Sn Anode with High Reversibility for Aqueous Batteries Enabled by "Water-in-Salt" Electrolyte

被引:12
|
作者
Ouyang, Jiaxing [1 ]
Wang, Yingming [1 ]
Wu, Nian [1 ]
Wang, Gongwei [1 ]
Xiao, Li [1 ]
Lu, Juntao [1 ]
Zhuang, Lin [1 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, Hubei Key Lab Electrochem Power Sources, Wuhan 430072, Peoples R China
来源
ACS APPLIED ENERGY MATERIALS | 2020年 / 3卷 / 05期
基金
中国国家自然科学基金;
关键词
tin anode for aqueous batteries; water-in-salt" electrolyte; dendrite-free; highly improved reversibility; Sn2+ hydrolysis; Sn/LiFePO4; cell; HYDROGEN EVOLUTION; HOLLOW CARBON; TIN; IMPEDANCE; MECHANISM; GROWTH;
D O I
10.1021/acsaem.0c00557
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
Metallic tin (Sn) has always been considered as an anode candidate for nonaqueous lithium-ion batteries (LIBs). Nevertheless, there were hardly any attempts to use Sn as an anode material in aqueous batteries. Although Sn possesses relatively high specific capacity (451.54 mAh/g, two-electron transfer reaction), mild electrode potential (-0.1375 V vs the standard hydrogen electrode, Sn2+ + 2e(-) = Sn), high hydrogen overpotential, and environmental friendliness, it also suffers from bad reversibility and low Coulombic efficiency (CE) in common aqueous electrolytes. In this work, a dendrite-free Sn anode with highly improved reversibility in an aqueous electrolyte was realized using a type of "water-in-salt" electrolyte (1 m Sn(OTf)(2) + 20 m LiTFSI). The results of Fourier transform infrared (FTIR) spectra and density functional theory (DFT) calculations have verified the significant impact of highly concentrated LiTFSI salt on Sn2+ hydrolysis, which is the key factor in improving the reversibility of the Sn anode and suppressing the dendrite formation. A Sn/LiFePO4 cell applying this electrolyte was acquired with a discharge plateau at around 0.6 V. In the cyclability test, the Sn anode exhibited a stable discharge capacity of more than 107 mAh/g with a Coulombic efficiency (CE) of 95% for 35 cycles (0.2C rate).
引用
收藏
页码:5031 / 5038
页数:8
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