Nanofibrous single metal oxides are promising electrode agents
for electrochemical supercapacitors (ESCs). However, their cycling
stability, capacitance, and rate efficiency still are required to
be promoted for practical applications. To boost electrochemical supercapacitor
(ESC) performance, it is critical to progressively develop a desirable
morphology and high-surface-area electrode material as well as to
design preferable electrode architecture. Therefore, we fabricated
the α-Fe2O3/Na2WO4 nanofibers (NFs) by one-step coaxial syringe electrospinning of
PVP-Fe(NO3)3 and PVP/Na2WO4 followed by the calcination of the product. Polyvinylidene fluoride/N-methyl-2-pyrrolidone solution containing different amounts
of as-prepared α-Fe2O3/Na2WO4 NFs with excellent processability and tolerability is prepared
followed by casting on conductive carbon cloth (CC) as a distinguished
electrode material, which satisfactorily reveals a specific capacitance
up to 265.54 F g–1 between −0.8 and 0.8 V
vs Ag/AgCl. The Cottrell and Dunn equations were applied to obtain
75.6% capacitive (non-faradaic) and 24.4% diffusion intercalation
(faradaic) current. The coin-cell-based symmetric structured ESC assembled
by two segments of CC-Fe2O3/Na2WO4 NF electrodes achieved 1.6 V operating voltage in 3.0 M Na2SO4 aqueous electrolyte and a specific capacitance
of 160 F g–1 with superficial cycling stability,
with 93% of initial capacitance retained after 200 cycles, revealing
rapid ion-captive redox reactions on Fe2O3/Na2WO4 NF surfaces. The CC-Fe2O3/Na2WO4 NF symmetric ESC can carry an energy
density of 50 Wh kg–1 at a power density of 514.28
W g–1. Our founding confirms that the CC-Fe2O3/Na2WO4 NF composite can
act as a promising ideal electrode material for high-performance symmetric
ESCs.