Bearing in mind that commercial LiBs use carbonate electrolytes which are recognized to pose safety issues and have been identified to suffer from degradation during charge-discharge cycles, we explored in this study the performance of Si anode in ionic liquid electrolytes based on phosphonium and pyrrolidinium cations, systems that are currently the most studied in the field of Li batteries [3-4]. Ionic liquid electrolytes are an appealing alternative to carbonates mainly because of their low volatility and better stability.
In the recent years, good electrochemical behavior has been observed in ionic liquids with high salt concentration [3-5]. In this work, we were able to demonstrate better electrochemical performance of Si anode in ionic liquid electrolytes with 3.2 m LiFSI compared to conventional carbonate electrolytes in terms of capacity and capacity retention at 50°C. Electrochemical performance obtained in the phosphonium and pyrrolidinium systems are compared for different concentrations and temperatures. Moreover, initial investigation of the SEI using NMR and XPS spectroscopy revealed that less degradation products are formed upon cycling in ionic liquid electrolytes compared to usual carbonates electrolytes. Overall, these results highlight the stability of ionic liquids which translate to good cycling performance and show promising potential of Si anode as a high-capacity material for high-energy and high-temperature applications. Cyclability and capacity retention for the phosphonium and pyrrolidinium system will be discussed in terms of ionic liquids components degradation and SEI formation and evolution, as probed by combined 19F, 7Li MAS-NMR, XPS and impedance spectroscopy.
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