Research demonstrates improved storage capacity and cycle life in potassium-ion battery anode, indicating better electronic conductivity and stability.
Although Ti-based polyanion anode materials with robust structures exhibit advantages such as high reversibility and high Coulombic efficiency for alkali metal-ion storage; however, their practical application is restricted by drawbacks including limited storage sites, low capacity, and intrinsically poor electronic conductivity. Herein, we propose a strategy of fluorine substitution combined with carbon coating of KTiOPO4 (KTPF/C), along with the introduction of K+ vacancies to activate additional potassium storage sites. The resulting KTPF/C material demonstrates a high capacity of 204.7 mAh g-1, corresponding to the reversible storage of 1.27 K+ ions. The synergistic effect of K+ vacancies and fluorine substitution not only lowers the operating voltage but also results in a more disordered structure, thereby reducing the volume change during potassiation/depotassiation to 7.3%. This enables an ultralong cycle life exceeding 20,000 cycles with an extremely low capacity fade rate of 0.011‰ per cycle. Moreover, the cooperation of K+ vacancies and carbon coating facilitates the transport of K+ and electrons, allowing the material to maintain excellent rate performance of 125.1 mAh g-1 at 5 A g-1. Practical full-cell testing further confirms the material's outstanding cycling stability, high power density, and all-climate applicability over a wide temperature range from -40 to 60 °C.
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Liao et al. (2025) studied this question.
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