RESUMEN
This work introduces a novel electrolyte comprising lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) salt dissolved in bio-based γ-valerolactone (GVL) for lithium-ion batteries (LIBs). Moreover, a simple and sustainable aqueous-based recycling approach for recovering the imide-based lithium salt is proposed. Beyond the sustainable origin of the GVL solvent, this electrolyte exhibits reduced flammability risk, characterized by a flash point of 136 °C, along with favorable transport properties (conductivity of 6.2 mS cm-1 at 20 °C) and good electrochemical stability (5.0 V vs Li+/Li). Its good compatibility with graphite and lithium iron phosphate electrodes ensures remarkable cycling stability in LIB full-cells after 200 galvanostatic cycles at 1 C. Furthermore, the proposed liquid-liquid phase electrolyte recycling method allows for a nearly complete recovery of the LiTFSI salt (97-99%) and the GVL solvent (78%). The feasibility of the recycling process is validated by the reutilization of the recovered LiTFSI salt in electric double-layer capacitors, achieving performances similar to that of the pristine salt with exceptional long-term stability.
RESUMEN
A comprehensive study on the properties and implementation of glyoxylic-acetals in sodium-ion energy storage systems is presented. Electrolytes containing 1,1,2,2-tetramethoxyethane (tetramethoxyglyoxal, TMG), 1,1,2,2-tetraethoxyethane (tetraethoxyglyoxal, TEG) and a mixture of the latter with propylene carbonate (PC) exhibit increased thermal stabilities and higher flash points compared to classical electrolytes based on carbonates as solvents. Due to its favorable properties, 1â m NaTFSI in TEG/PC (3 : 7), has been selected and used for sodium-ion energy storage systems based on a Prussian Blue (PB) positive electrode and a hard carbon (HC) negative electrode. Compared to conventional electrolyte (based on a 1 : 1 mixture of ethylene carbonate, EC, and dimethyl carbonate, DMC), this glyoxylic-acetal electrolyte provides competitive capacity and prolonged cycle life. Postmortem XPS analysis indicates that the electrode-electrolyte interphases formed in presence of TEG are thicker and presumably more protective, inhibiting typical degradation processes of the electrodes. Furthermore, it is demonstrated that the suitable properties of TEG on the cycling stability can also be exploited for the construction of highly stable sodium-ion capacitors.