Sodium-conducting electrolytes, based on the EMIFSI, EMITFSI, N1114FSI, N1114TFSI, N1114IM14, PIP13TFSI and PIP14TFSI ionic liquids, were investigated in terms of electrochemical stability through voltammetry techniques with the aim of evaluating their feasibility in Na-ion devices. Both the anodic and cathodic sides were studied. The effect of contaminants, such as water and/or molecular oxygen, on the electrochemical robustness of the electrolytes was also investigated. Preliminary cyclic voltammetry and charge-discharge tests were carried out in Na/hard carbon and Na/α-NaMnO2 half cells using selected ionic liquid electrolytes. The results are presented and discussed in the present paper.

Silicon nanowire anodes were investigated in lithium-metal cells using different electrolyte formulations based on 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide, 1-ethyl-3-methylimidazolium bis(fluorosulfonyl)imide and N -trimethyl-N -butyl-ammonium bis(fluoro sulfonyl)imide ionic liquids. The lithium insertion process in the silicon anode was analyzed by cyclic voltammetry measurements, performed at different scan rates and for prolonged cycles, combined with impedance spectroscopy analysis. A galvanostatic charge-discharge cycling test was performed to analyze the electrochemical performances using different types of ionic liquids. A study of the Solid Electrolyte Interphase layer on the silicon nanowire electrode surface was carried out through X-ray photoelectron spectroscopy. In general, the silicon anodes in 1-ethyl-3-methylimidazolium bis(fluorosulfonyl)imide-based electrolytes show very good reversibility, reproducibility, and efficiency in the lithiation process, even at high scan rates, and exhibit a reversible capacity exceeding 1,000 mA h g-1 after 2,000 charge-discharge cycles, corresponding to 46% of the initial value.

Hard carbons (HC) from natural biowaste have been investigated as anodes for sodium‐ion batteries in electrolytes based on 1‐ethyl‐3‐methylimidazolium bis(fluorosulfonyl)imide ([EMI][FSI]) and N‐trimethyl‐N‐butylammonium bis(fluorosulfonyl)imide ([N1114][FSI]) ionic liquids. The Na⁺ intercalation process has been analyzed by cyclic voltammetry tests, performed at different scan rates for hundreds of cycles, in combination with impedance spectroscopy measurements to decouple bulk and interfacial resistances of the cells. The Na⁺ diffusion coefficient in the HC host has been also evaluated via the Randles‐Sevcik equation. Battery performance of HC anodes in the ionic liquid electrolytes has been evaluated in galvanostatic charge/discharge cycles at room temperature. The evolution of the SEI (solid electrochemical interface) layer grown on the HC surface has been carried out by Raman spectroscopy. Overall the sodiation process of the HC host is highly reversible and reproducible. In particular, a capacity retention exceeding 98 % of the initial value has been recorded in[N1114][FSI] electrolytes after more than 1500 cycles with a coulombic efficiency above 99 %, largely beyond standard carbonate‐based electrolytes. Raman, transport properties and impedance confirms that ILs disclose the formation of SEI layers with superior ability to support the reversible Na+ intercalation with the possible minor contributions from the EMI+cation.