The ionic liquid (IL) N -methyl- N -butylmorpholinium bis(fluorosulfonyl)imide (C 4 mmor FSI) is examined from physical and electrochemical perspectives. Pulsed field gradient NMR spectroscopy shows that ion diffusivities are low compared with similar, non-ethereal ILs. Ionicity values indicate that above room temperature, less than 50% of ions contribute to conductivity. Lithium cycling in symmetrical cells using a C 4 mmor FSI-based electrolyte is best demonstrated at elevated temperatures. Specific capacities of 130 mAh g −1 are achieved in a Li−LiFePO 4 battery at 85 °C. FT-IR spectroscopic investigations of lithium electrodes suggest the presence of alkoxide species in the solid electrolyte interphase (SEI), implying a ring-opening reaction of C 4 mmor with lithium metal. In contrast, the SEI derived from N -methyl- N -propylpiperidinium FSI lacks the alkoxide signature but shows signs of alkyl unsaturation, and the activation energy for Li + transport through this SEI is slightly lower than that for the C 4 mmor-derived SEI. Our detailed findings give insight into the capabilities and limitations of rechargeable lithium metal batteries utilizing a C 4 mmor FSI electrolyte.
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Lane et al. (2010) studied this question.
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