Ferdousi Shammi A, Hilder Matthias, Basile Andrew, Zhu Haijin, O'Dell Luke A, Saurel Damien, Rojo Teofilo, Armand Michel, Forsyth Maria, Howlett Patrick C
Institute for Frontier Materials (IFM), Deakin University, Burwood, Victoria, 3125, Australia.
CIC Energigune, Alava Technology Park, Albert Einstein 48, 01510, Miñano Àlava, Spain.
ChemSusChem. 2019 Apr 23;12(8):1700-1711. doi: 10.1002/cssc.201802988. Epub 2019 Mar 28.
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 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 ) 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 (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|NaFePO 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.
研究了水对离子液体(ILs)中超浓钠盐溶液性质的影响,旨在设计以水为添加剂的钠电池应用电解质。将水添加到50 mol %的双(氟磺酰)亚胺钠(NaFSI)[FSI = 双(氟磺酰)亚胺]在离子液体N-甲基-N-丙基吡咯烷鎓双(氟磺酰)亚胺(C mpyrFSI)中的溶液中。尽管热性质(如玻璃化转变温度)对水含量的依赖性很小,但粘度,尤其是离子电导率受到强烈影响。Na|Na对称电池的循环性能强烈依赖于施加的电流密度以及水含量。在较高电流密度(1.0 mA cm )下,极化曲线显示出对水的依赖性,这表明水积极参与了高水含量样品(1000 - 5000 ppm)中改进的固体电解质界面层(SEI)的形成,从而提高了长期循环稳定性。在1.0 mA cm 下循环的电池(在20次循环后测量)的初始阻抗在加水后升高,并且“湿”样品出现大的极化。然而,随着进一步循环,与“干”样品相比,湿电池开始表现出更低的极化和更好的稳定性。还展示了Na|NaFePO电池的循环性能,对电池容量的影响最小,进一步突出了水在这些电解质体系中的活性可忽略不计。实际上,加水后电池极化降低且电荷分布更清晰。此处所示的工作表明,水可作为超浓钠IL电解质的方便且廉价的添加剂,以改善器件性能。