Alluaudite-type Na2+2xFe2-x(SO4)3 (NFS) with high theoretical energy density is regarded as the promising cathode of sodium-ion batteries (SIBs), while practical rate and cyclic performances are still hindered by intrinsic poor conductivity. Here, a facile method is developed, collaborating high-boiling organic solvents assisted colloidal synthesis (HOS-CS) with sintering for tailoring Na2Fe2(SO4)3 nanocrystals decorated by conductive carbon network toward high-rate-capability cathode of SIBs. Impressively, the as-prepared Na2Fe2(SO4)3@MC provides 60.6 and 46.9 mAh g-1 of reversible capacities even at ultrahigh rates of 20 and 30 C, respectively, ranking the superior state among the current NFS-based cathode. More importantly, Na2Fe2(SO4)3@MC achieves 73% of capacity retention at 20 C after 500 cycles, highlighting its potential for application as a fast chargeable cathode. As a bonus, the full-cell configuration constructed with Na2Fe2(SO4)3@MC cathode and commercial hard carbon (HC) anode delivers 45.6 mAh g-1 at 10 C and 68.3 mAh g-1 of initial capacity with ≈79.4% of retention after 100 cycles at 2 C. Also, Na2Fe2(SO4)3@MC||HC full cell supplies as high as 140 Wh kg-1 of practical energy density. This work offers a novel approach to prepare NFS cathode for SIBs with both high energy density and fast-charging ability.
Keywords: alluaudite‐type Na2+2xFe2‐x(SO4)3; colloidal synthesis; high energy density; high‐rate capability; sodium‐ion batteries.
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