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Comparative Study of M[N(SO2F)(SO2CF3)]–[N‑Butyl‑N‑methylpyrroridinium][N(SO2F)(SO2CF3)] (M = Li, Na, K, Rb, Cs) Ionic Liquid Electrolytes

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journal contribution
posted on 15.09.2020, 03:43 by Takayuki Yamamoto, Shu Nishijima, Toshiyuki Nohira
We systematically evaluated the physicochemical properties of a series of M­[FTA]–[C4C1pyrr]­[FTA] ionic liquids (ILs) (M = alkali metal, FTA = (fluorosulfonyl)­(trifluoromethylsulfonyl)­amide, C4C1pyrr = N-butyl-N-methylpyrrolidinium) as electrolytes for alkali metal-ion batteries. First, the viscosity (η), ionic conductivity (σ), and density (ρ) of the M­[FTA]–[C4C1pyrr]­[FTA] ILs at x(M­[FTA]) = 0.20 (x(M­[FTA]) = molar fraction of M­[FTA]) were measured. The σ values ranged from 1–3 mS cm–1 at 298 K and increased as follows: Na < Li < K < Rb < Cs, which indicated that the Li-based IL did not obey the trend predicted by the charge densities of alkali metal cations. Second, the Li-based IL exhibited slightly lower vertical intercept values than the other FTA-based ILs in the Walden plots obtained using the results of η, σ, and ρ measurements. Third, the electrochemical stability of the ILs was investigated by cyclic voltammetry, and the redox potentials of the alkali metals (E(M+/M)) were determined. The E(M+/M) values of the FTA-based ILs increased as follows: Cs < Rb < K < Li < Na. Subsequently, we compared the obtained E(M+/M) values with those of other general electrolytes, such as propylene carbonate (PC)-based electrolytes and aqueous solutions. The trend in E(M+/M) values of the FTA-based ILs was similar to that of PC-based electrolytes and was significantly different from that of aqueous solutions. In particular, the FTA- and FSA-based ILs (FSA = bis­(fluorosulfonyl)­amide) presented the most negative E(Na+/Na) and E(K+/K) values among various electrolytes, which indicated that utilization of these IL electrolytes for the development of Na- and K-ion batteries would present significant advantages.

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