Continuous side reactions between the biomass-derived hard carbon surface and the electrolyte affect its cycling stability and fast-charging performance. Therefore, constructing a stable solid electrolyte interface (SEI) while facilitating easier desolvation of sodium ions in the electrolyte is key to achieving stable fast charging. Theoretical calculations confirm that Na3P can induce the formation of a Na+ solvation structure with low solvent coordination, thus achieving a lower desolvation energy barrier and faster Na+ diffusion capability through the SEI. We used bamboo powder, partially de-lignified, as a precursor for hard carbon. After sublimating red phosphorus in a sealed tube and cooling deposition, a phosphide layer was constructed on the hard carbon surface. During charge-discharge cycling, a SEI enriched with Na3P components was formed on the surface. The final full cell assembled with HC-3wt% P matched with the cathode exhibited excellent rate performance, with a reversible discharge capacity of 78 mAh g-1 at 10 C, significantly outperforming the performance of recently reported bamboo powder-based hard carbon. The assembled pouch cell maintained stable cycling for 1000 cycles at 0.5 C. This work provides guidance from the perspective of SEI regulation and design for enhancing the fast-charging performance of biomass-derived hard carbon anodes in sodium-ion batteries.
