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Graphite shows great potential as an anode material for rechargeable metal-ion batteries because of its high abundance and low cost. However, the electrochemical performance of graphite anode materials for rechargeable potassium-ion batteries needs to be further improved. Reported herein is a natural graphite with superior rate performance and cycling stability obtained through a unique K+ -solvent co-intercalation mechanism in a 1 m KCF3 SO3 diethylene glycol dimethyl ether electrolyte. The co-intercalation mechanism was demonstrated by ex situ Fourier transform infrared spectroscopy and in situ X-ray diffraction. Moreover, the structure of the K-solvent+ complexes intercalated with the graphite and the conditions for reversible K+ -solvent co-intercalation into graphite are proposed based on the experimental results and first-principles calculations. This work provides important insights into the design of natural graphite for high-performance rechargeable potassium-ion batteries.
Li et al. (Thu,) studied this question.