Na3V2(PO4)3 (NVP) materials
have emerged as a promising cathode for sodium ion batteries (SIBs).
Herein, NVP is successfully optimized by dual-doping K/Co and enwrapping
carbon nanotubes (CNTs) through a sol–gel method. Naturally,
the occupation of K and Co in the Na1 sites and V sites can efficiently
stabilize the crystal cell and provide the expanded Na+ transport channels. The existence of tubular CNTs could restrict
the crystal grain growth and effectively downsize the particle size
and provide a shorter pathway for the migration of electrons and ions.
Moreover, the amorphous carbon layers combined with the conductive
CNTs form a favorable network for the accelerated electronic transportation.
Furthermore, the ex situ XPS characterization reveals that an extra
redox reaction pair of Co2+/Co3+ is successfully
activated at the high voltage range, resulting in superior capacity
and energy density property for KC0.05/CNTs composites. Comprehensively,
the optimized KC0.05/CNTs electrode exhibits a distinctive electrochemical
property. It delivers an initial reversible capacity of 119.4 mA h
g–1 at 0.1 C, surpassing the theoretic value for
the NVP system (117.6 mA h g–1). Moreover, the KC0.05/CNT
electrode exhibits the initial capacity of 113.2 mA h g–1 at 5 C and 105.8 mA h g–1 at 10 C, and the maintained
capacities at 500 cycles are 105.8 and 100.8 mA h g–1 with outstanding retention values of 96.6 and 95.3%. Notably, it
releases capacities of 99.8 and 84.5 mA h g–1 at
50 and 100 C, and the capacity retention values at 2500 cycles are
66.2 and 58.8 mA h g–1, respectively. What is more,
the KC0.05/CNTs//Bi2Se3 asymmetric full cell
exhibits a high capacity of 191.4 mA h g–1 at 2.65
V, with the energy density being as high as 507 W h kg–1, demonstrating the eminent practical application potential of KC0.05/CNTs
in SIBs.