Abstract
Sodium iron phosphate (NaFePO(4)) has attracted significant attention because of its high theoretical capacity (155 mA h g(-1)), remarkable structural stability, and abundant elemental composition. However, the electrochemical reversibility of maricite NaFePO(4) is generally considered inactive. Herein, a nanoengineering strategy to activate the electrochemical activity of maricite NaFePO(4) is presented. This approach involves the construction of ultrasmall maricite NaFePO(4) nanoparticles encapsulated within an ultrathin carbon layer (denoted as m-NFP@C), which greatly improves the electrochemical properties of the material. Notably, the optimized m-NFP@C nanoparticles exhibit an impressive reversible capacity of 101.4 mA h g(-1) after 100 cycles at a current density of 20 mA g(-1), demonstrating a remarkable capacity retention of 90.5%. Furthermore, when coupled with the bismuth-carbon microfoam-like compound (Bi@NC-MF) anode, the fabricated sodium-ion full cell exhibits exceptional cycling stability with a capacity retention of 90.6% over 250 cycles. The remarkable electrochemical performance of this material can be attributed to its excellent structural stability, ultrafine nanostructure, and uniform carbon coating, which effectively shorten the Na(+) diffusion pathways, prevent the aggregation and fragmentation of nanoparticles, and enhance electronic conductivity. This work is anticipated to open up a new route for activating maricite NaFePO(4) and advancing the development of polyanion-type electrode materials.