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Effect of Electrolyte Composition on Performance and Stability of Lithium-Sulfur Batteries

Monday, 1 October 2018: 09:00
Galactic 7 (Sunrise Center)
Y. Ishino, K. Takahashi, W. Murata (Kogakuin University), M. Watanabe (Yokohama National University), and S. Seki (Current affiliation: Kogakuin University)
Rechargeable lithium-ion batteries (LIBs) are necessary for our life to use as a mobile phone and so on. Lithium-sulfur (Li-S) battery is expected for next generation rechargeable battery owing to have high capacity (1,645 mAh/g) compared with conventional Li-ion batteries. Cycle performances are one of the index of battery. There is strongly related with a battery lifetime. The key issues of Li-S battery for cycle performances are the dissolution of sulfur species, the positive electrode active material, as Li2Sx (lithium polysulfide). If we can suppress the dissolution of Li2Sx, the battery life should be extended. Solvate ionic liquid (SIL) is mixture of 1:1 complex from low-molecular weight ether and Li salt, which have high thermal/electrochemical stabilities owing to strong interaction of between ether oxygen and Li cation. Also SIL electrolyte can suppress the dissolution of Li2Sx. Recently, high Li salt concentration more than conventional SIL into electrolyte is important for high performance LIBs and Li-S batteries not only the high stability but also low Lewis basicity of electrolytes for low solubility of impurity with charge/discharge. Fig. 1 shows cycle performance of LiNi1/3Mn1/3Co1/3O2 | [Li(G3)x]TFSA | Li cell. Excess Li salts achieved high cycle performances and stable charge-discharge operations [1]. Fig. 2 shows Charge-discharge profiles with C/18(Li-S | [Li(G3)1]TFSA | Li cell). Over 1,000 mAh/g capacity at 1st charge-discharge, and 600 mAh/g capacity at 600 cycles were observed. We consider to importance for composition ratio glyme and LiTFSA for lithium-sulfur battery performance [2].However, quantitative analysis for dissolution of Li2Sx into various SIL ([Li(G3)x] [TFSA]) has not investigated. In this study, to clarify relationship between composition ratio and dissolution amount of Li2Sx, saturated solubility of Li2Sx was measured by electrochemical and UV-vis spectra.

All experiments were examined in a glove box with Ar atmosphere. SILs, [Li(G3)1.25]TFSA, [Li(G3)1.11]TFSA, [Li(G3)]TFSA, [Li(G3)0.9]TFSA and [Li(G3)0.8]TFSA (composition ratio of glyme (G3,tryglyme) and LiTFSA is 10:8, 10:9, 10:10, 10:9 and 10:8), were prepared. Mixture of S8 and Li2S (S8:Li2S=7:8, we defined as Li2S8) were prepared. SILs of each concentration ratio prepared with Li2S8 was stirred to a saturated state with a hot stirrer at 50 ℃. It was oxidized to S8 by holding it at 3.0V for 12h using an electrolytic cell. The electrolytic and non-electrolytic SILs were each diluted 40 times (molar ratio) with HFE, and the absorbance was measured by UV-vis spectrometer. Lithium-sulfur batteries using electrolytes of each composition were prepared and charge and discharge cycle tests were carried out.

Fig. 3 shows appearances of five LiTFSA concentration SILs with saturated Li2S8. This shows high concentration lithium salt electrolyte suppresses dissolution of Li2Sx into each SILs. Fig. 4 shows UV-vis spectra of non- or electrolytic SILs. Color strength (dark to yellow) were decreased with Li salt concentration into SILs, and considered the solubility of Li2Sx was controlled with the Li salt concentrations. We confirmed that improvement in cycle performances were observed in the lithium-sulfur batteries using various lithium salt concentration SILs. In the presentation, we will report to results of UV-vis spectra and correlation of between dissolution amount of Li2Sx and battery performances.

References:

[1] Seki et. al, RSC Adv., 6, 33049-33047 (2016).

[2] Seki et. al, Electrochem., 85, 680-682 (2017).