Highly Concentrated NaN(SO2F)2/3-Methylsulfolane Electrolyte Solution Showing High Na-Ion Transference Number under Anion-Blocking Conditions

被引:9
作者
Tatara, Ryoichi [1 ,4 ]
Okamoto, Yukihiro [1 ]
Ugata, Yosuke [1 ]
Ueno, Kazuhide [1 ,2 ]
Watanabe, Masayoshi [1 ,2 ]
Dokko, Kaoru [1 ,2 ,3 ]
机构
[1] Yokohama Natl Univ, Dept Chem & Life Sci, Hodogaya Ku, 79-5 Tokiwadai, Yokohama, Kanagawa 2408501, Japan
[2] Yokohama Natl Univ, Adv Chem Energy Res Ctr ACERC, Inst Adv Sci, Hodogaya Ku, 79-5 Tokiwadai, Yokohama, Kanagawa 2408501, Japan
[3] Kyoto Univ, Unit Elements Strategy Initiat Catalysts & Batter, Nishikyo Ku, Goryo Ohara, Kyoto 6158245, Japan
[4] Tokyo Univ Sci, Dept Appl Chem, Shinjuku Ku, 1-3 Kagurazaka, Tokyo 1628601, Japan
基金
日本学术振兴会;
关键词
Sodium Batteries; Ligand Exchange; Transference Number; Concentration Polarization; SUPERCONCENTRATED ELECTROLYTES; NEGATIVE ELECTRODES; SODIUM; SOLVATION;
D O I
10.5796/electrochemistry.21-00095
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The performance of a sodium-ion (Na) battery is significantly influenced by its electrolyte characteristics. In particular, the transport properties of the electrolyte have considerable effects on the discharge rate capability. During discharging of a Na battery at high current densities, a concentration gradient of Na salt develops because both cations and anions are mobile in the liquid electrolyte. Concentration polarization can be suppressed by increasing the Na+ transference number (t(Na+)) of the electrolyte. This study demonstrates that highly concentrated NaN(SO2F)(2) dissolved in 3-methylsulfolane (MSL) exhibits a high t(Na+) value of >0.6 under anion-blocking conditions. Raman spectroscopy revealed that Na+ ions formed complexes with MSL and anions in the electrolyte. Na+ ions exchange ligands dynamically and move faster than the ligands, resulting in a high t(Na+). The high t(Na+ )enables a high-rate discharge of the Na battery, despite the low ionic conductivity of the highly concentrated electrolyte. (C) The Author(s) 2021. Published by ECSJ.
引用
收藏
页码:590 / 596
页数:7
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