Abstract
Transition metal oxides with high theoretical specific capacity, when used as anode materials in sodium-ion batteries, usually suffer from poor structural stability and inferior rate capacity. The use of hollow nanostructured metal oxides incorporated into porous carbon frameworks is a promising strategy for addressing this issue. Herein, we fabricated hollow Co3O4 nanoparticles anchored in a porous carbon nanofiber matrix (Co3O4@PCNF) by electrospinning, metal–organic framework incorporation, and two-step calcination. The porous carbon nanofiber matrix can facilitate structural stability and provide multiple channels for fast electron/ion transport. The hollow Co3O4 nanoparticles resulting from the Kirkendall effect can shorten the Na-ion transport path for achieving fast reaction kinetics. The Co3O4@PCNF exhibits a reversible specific capacity of 487 mAh g−1 at 0.05 A g−1 with a high initial Coulombic efficiency of 91.6%, outstanding rate performance (220 mAh g−1 at 5 A g−1), and stable cycling, thereby making it suitable as an anode for sodium-ion batteries. Moreover, a full cell fabricated using a Co3O4 @PCNF anode and Na3V2(PO4)2O2F cathode delivers a reversible capacity of 205 mAh g−1 at 0.5 A g−1. We believe that our approach can provide a design pathway to improve the performance of Co3O4-based anodes for sodium-ion batteries and offer a new strategy to produce hollow-structure electrode materials for other energy-storage devices.
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