Reversible Zinc Electrodeposition at-60 °C Using a Deep Eutectic Electrolyte for Low-Temperature Zinc Metal Batteries

被引:12
|
作者
Hawkins, Brendan E. [1 ]
Schoetz, Theresa [1 ]
Gordon, Leo W. [1 ]
Surabh, K. T. [1 ]
Wang, Jonah [1 ]
Messinger, Robert J. [1 ]
机构
[1] CUNY City Coll, Dept Chem Engn, New York, NY 10031 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2023年 / 14卷 / 09期
基金
美国国家航空航天局; 美国国家科学基金会;
关键词
PARTICLE MESH EWALD; LIQUID ELECTROLYTES; LITHIUM BATTERIES; FORCE-FIELD; PARAMETERS; HYBRID;
D O I
10.1021/acs.jpclett.3c00150
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
Rechargeable zinc (Zn) metal batteries are attractive for use as electrochemical energy storage systems on a global scale because of the low cost, high energy density, inherent safety, and strategic resource security of Zn metal. However, at low temperatures, Zn batteries typically suffer from high electrolyte viscosity and unfavorable ion transport properties. Here, we studied reversible Zn electrodeposition in mixtures of 1-ethyl-3-methyl-imidazolium bis(trifluoromethylsulfonyl)imide ([EMIm]TFSI) ionic liquid, gamma-butyrolactone (GBL) organic solvent, and Zn(TFSI)2 zinc salt. The electrolyte mixtures enabled reversible Zn electrodeposition at temperatures as low as -60 degrees C. An electrolyte composed of 0.1 M Zn(TFSI)2 in [EMIm]TFSI:GBL with a volume ratio of 1:3 formed a deep eutectic solvent that optimized electrolyte conductivity, viscosity, and the zinc diffusion coefficient. Liquid state 1H and 13C nuclear magnetic resonance (NMR) spectroscopy and molecular dynamic (MD) simulations indicate increased formation of contact ion pairs and the reduction of ion aggregates are responsible for the optimal composition.
引用
收藏
页码:2378 / 2386
页数:9
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