Manipulating amorphous and crystalline hybridization of Na3V2(PO4)3/C for enhancing sodium-ion diffusion kinetics

Na3V2(PO4)3 (NVP) has attracted considerable attention as a promising cathode material for sodium-ion batteries (SIBs). But its insufficient electronic conductivity, limited capacities, and fragile structure hinder its extended application, particularly in scenarios involving rapid charging and prolonged cycling. A hybrid cathode material has been developed to integrate both amorphous and crystalline phases, with the objective of improving the rate performance and Na storage capacity by leveraging bi-phase coordination. Consequently, the combination of amorphous and crystalline phases enhanced the kinetics of Na-ion diffusion, resulting in a 1–2 orders of magnitude enhancement in diffusion dynamics. Furthermore, the existence of amorphous states has been demonstrated to elevate the active Na2 site content, resulting in an increased reversible capacity. This assertion is substantiated by evidence derived from solid-state nuclear magnetic resonance (ss-NMR) and electrochemical characteristics. The innovative bi-phase collaborative material provides a specific capacity of 114 mAh/g at 0.2 C, exceptional rate performance of 82 mAh/g at 10 C, and remarkable long-term cycle stability, retaining 95 mAh/g at 5 C even after 300 cycles. In conclusion, the homogeneous hybridization of amorphous and crystalline phases presents itself as a promising and effective strategy for improving Na-ion storage capacity of cathodes in SIBs.