摘要
It is highly desirable for the promising sodium storage possessing high rate and long stable capability, which are mainly hindered by the unstable yet conventional solvent-derived organic-rich solid electrolyte interphases. Herein, an electrolyte solvation chemistry is elaborately manipulated to produce an enhanced anion-derived and inorganic components-dominated solid electrolyte interphases by introducing a low permittivity (4.33) bis(2,2,2-trifluoroethyl) ether diluent into the sodium bis(trifluoromethylsulfonyl)imide-dimethoxyethane-based high concentration electrolyte to obtain a localized high concentration electrolyte. The bis(2,2,2-trifluoroethyl) ether breaks the balance of original cation solvation structure and tends to interact with Na + -coordinated dimethoxyethane solvent rather than Na + in high concentration electrolyte, leaving an enhanced Coulombic interaction between Na + and (FSO 2 ) 2 N − , and more (FSO 2 ) 2 N − can enter the Na + solvation shell, forming a further increased number of Na + -(FSO 2 ) 2 N − -dimethoxyethane clusters (from 82.0% for high concentration electrolyte to 94.3% for localized high concentration electrolyte) at a low salt dosage. The preferential reduction of this (FSO 2 ) 2 N − -enriched clusters rather than the dimethoxyethane-dominated Na + solvation structure produces an enhanced anion-derived and inorganic components-dominated solid electrolyte interphases. The reversible charge storage process of Na is decoupled by operando Raman along with a shift of D and G peaks. Benefiting from the enhanced anion-derived electrode-electrolyte interface, the commercial hard carbon anode in localized high concentration electrolyte shows a well rate capability (5 A g −1 , 70 mAh g −1 ), cycle performance and stability (85% of initial capacity after 700 cycles) in comparison to that of high concentration electrolyte (68%) and low concentration electrolyte (only 5% after 400 cycles), indicative of uniqueness and superiorities towards stable Na storage.
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