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Abstract Na 3 V 2 (PO 4 ) 2 F 3 is an attractive cathode for sodium‐ion batteries due to its stable structure, high voltage, and impressive energy density. Nonetheless, its practical application is constrained by sluggish Na + diffusion kinetics and inferior rate capability, stemming from insufficient electronic conductivity, strong Coulombic attraction between mobile Na + with F − , and electrostatic repulsion among neighboring ions. Herein, Li‐doped Na 2.9 Li 0.1 V 2 (PO 4 ) 2 F 3 is obtained to regulate the electronic environment within Na + diffusion channels. Theoretical calculations indicate that Li doping reduces electron density surrounding pendant F − and mitigates repulsive forces between adjacent Na + through electrostatic shielding, facilitating Na + mobility. Li doping also disrupts the ordered Na + arrangement, lowering the energy barrier for ion migration. Besides, the integration of carbon nanotube network and carbon‐coated aluminum foil substrate enhances external electronic conductivity and reduces polarization. In situ electrochemical impedance spectroscopy and distribution of relaxation times techniques confirm that these strategies lower charge transfer resistance during the sodium storage process. Hence, the optimized electrode delivers enhanced rate capability (75.27 mAh g −1 at 50C) and outstanding long‐term cycling stability (with a capacity decay of only 0.0012% per cycle over 30000 cycles at 10C) in half‐cells and excellent rate performance across wide temperature range in full‐cells.
Lin et al. (Thu,) studied this question.