The Relationship between the Relative Solvating Power of Electrolytes and Shuttling Effect of Lithium Polysulfides in Lithium-Sulfur Batteries

被引:73
|
作者
Su, Chi-Cheung [1 ]
He, Meinan [1 ]
Amine, Rachid [2 ]
Chen, Zonghai [1 ]
Amine, Khalil [1 ,3 ]
机构
[1] Argonne Natl Lab, Chem Sci & Engn Div, 9700 S Cass Ave, Argonne, IL 60439 USA
[2] Argonne Natl Lab, Mat Sci Div, 9700 S Cass Ave, Argonne, IL 60439 USA
[3] Stanford Univ, Mat Sci & Engn, Stanford, CA 94305 USA
关键词
batteries; electrochemistry; NMR spectroscopy; relative solvating power; structure-activity relationships; FLUORINATED ETHER; ION BATTERIES; PERFORMANCE; COSOLVENT; LI+;
D O I
10.1002/anie.201807367
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Relative solvating power, that is, the ratio of the coordination ratios between a solvent and the reference solvent, was used to probe the quantitative structure-activity relationship of electrolyte solvents and the lithium polysulfide (LiPS) dissolution in lithium-sulfur batteries. Internally referenced diffusion-ordered nuclear magnetic resonance spectroscopy (IR-DOSY) was used to determine the diffusion coefficient and coordination ratio, from which the relative solvating power can be easily measured. The higher the relative solvating power of an ethereal solvent, the more severe will be the LiPS dissolution and the lower the coulombic efficiency of the lithium-sulfur battery. A linear relationship was established between the logarithm of relative solvating power of a solvent and the degree of LiPS dissolution, rendering relative solvating power an important parameter in choosing the electrolyte solvent for lithium-sulfur batteries.
引用
收藏
页码:12033 / 12036
页数:4
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