Tunning solvation structure in non-flammable, localized high-concentration electrolytes with enhanced stability towards all aluminum substrate-based K batteries

Abstract

Although metallic potassium or graphite anode with low redox potentials are desirable for potassium-ion batteries (PIBs), the severe capacity decay caused by consecutive reduction reactions on the aggressively reactive anode surface is inevitable because of the scarcity of an effective passivation layer. Additionally, the development of PIBs faces potential safety hazards due to the usage of reactive anodes with flammable electrolytes. Herein, a fire-retardant localized high-concentration electrolyte (LHCE) is formulated by adding a low-polarity co-solvent of highly fluorinated ether into the concentrated potassium bis(fluorosulfonyl)imide/trimethyl phosphate. A unique electrolyte solvation environment with the enhanced anion-cation interaction in an LHCE facilitates a durable anion-derived solid electrolyte interphase (SEI) with self-accelerated interfacial kinetics and minimizes the SEI dissolution compared to the conventional carbonate-based electrolyte. Consequently, the unmodified Al substrate could sustain stable potassium metal cycling above 3400 h (over 800 cycles) with high reversibility (98%), and the graphite anode retains prolonged cyclic stability (over 300 cycles) with a high reversible capacity (257.6 mAh g−1) and capacity retention (92.6 % at 0.2 C). Meanwhile, Al corrosion at high voltage is significantly suppressed, and the electrochemical window is extended due to less free solvents in an LHCE, enabling good electrolyte compatibility with high-voltage cathodes. Coupling non-flammable solvents and the concept of LHCE could facilitate a better understanding of electrolyte chemistry and offer more opportunities to use K or graphite anode for all Al substrate-based PIBs highlighted with high performance and superb safety.