Water as an Effective Additive for High-Energy-Density Na Metal Batteries? Studies in a Superconcentrated Ionic Liquid Electrolyte

被引:37
作者
Ferdousi, Shammi A. [1 ]
Hilder, Matthias [1 ]
Basile, Andrew [1 ]
Zhu, Haijin [1 ]
O'Dell, Luke A. [1 ]
Saurel, Damien [2 ]
Rojo, Teofilo [2 ]
Armand, Michel [2 ]
Forsyth, Maria [1 ]
Howlett, Patrick C. [1 ]
机构
[1] Deakin Univ, IFM, Burwood, Vic 3125, Australia
[2] CIC Energigune, Alava Technol Pk,Albert Einstein 48, Minano Alava 01510, Spain
基金
澳大利亚研究理事会;
关键词
batteries; bis(fluorosulfonyl)imide; ionic liquids; sodium; water; METHYLPYRROLIDINIUM BIS(FLUOROSULFONYL)IMIDE; TRANSPORT-PROPERTIES; TRANSFERENCE NUMBER; NAFEPO4; MECHANISM; BEHAVIOR; CHALLENGES; SOLVATION; DIFFUSION; STATE;
D O I
10.1002/cssc.201802988
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The effect of water on the properties of superconcentrated sodium salt solutions in ionic liquids (ILs) was investigated to design electrolytes for sodium battery applications with water as an additive. Water was added to a 50 mol % solution of NaFSI [FSI=bis(fluorosulfonyl)imide] in the ionic liquid N-methyl-N-propylpyrrolidinium bis(fluorosulfonyl)imide (C(3)mpyrFSI). Although the thermal properties (e.g., glass transition temperature) showed little dependence on the water content, the viscosity and, in particular, the ionic conductivity were strongly affected. The Na|Na symmetrical cell cycling performance was strongly dependent on the applied current density as well as on the water content. At higher current densities (1.0 mA cm(-2)) the polarization profiles showed a water dependence, suggesting that water was actively involved in the formation of an improved solid electrolyte interface layer (SEI) for high-water-content samples (1000-5000 ppm), resulting in improved long-term cycling stability. The initial impedance of cells cycled at 1.0 mA cm(-2) (measured after 20 cycles) was elevated after water addition, and large polarizations occured for the "wet" samples. However, with further cycling the wet cells began to exhibit lower polarization and improved stability compared to the "dry" sample. The Na|NaFePO4 cell cycling performance was also demonstrated with minimal effect on the cell capacity, further highlighting the negligible activity of water in these electrolyte systems. In fact, reduced cell polarization and a more clearly defined charge profile were evident after water addition. The work shown here suggests that water may be used as a convenient and inexpensive additive for superconcentrated sodium IL electrolytes for improved device performance.
引用
收藏
页码:1700 / 1711
页数:12
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