To
meet the demand for the development of high energy storage devices,
appropriate designs of advanced carbon nanostructures (CNs) with metal
oxides are highly preferred. Herein, the surfaces of two advanced
carbon nanostructures (CNs), g-C3N4 and carbon
nanofibers, were modified by the addition of carboxyl functional groups
and then bound to TiO2 nanospheres (TNS). The surface functionalization
of CNs is an efficient approach for improving the performance of carbon-based
supercapacitors by solving the dispersion problems. Field emission
scanning electron microscopy and transmission electron microscopy
images demonstrated the sheet, fiber, and sphere morphologies of g-C3N4, carbon, and TiO2, respectively.
According to the results of Fourier transform infrared spectroscopy,
the carboxyl functional groups with CNs were confirmed. In a three-electrode
system, the supercapacitance of fictitious electrodes was evaluated
with a 4 M KOH electrolyte. The surface-functionalized hybrid electrode
showed a specific capacitance (817 F g–1) at a current
density of 0.25 A g–1 superior to those of the other
fictitious electrodes. The electrode showed stability for up to 2000
cycles, with 89.2% capacitance retention. The superior electrochemical
properties of CNs–TNS were attributed to the synergetic effects
of g-C3N4–CNF/TiO2 composition
and its excellent accessibility, conductivity, surface functionalization,
and strong chemical interface. This study positively encourages the
manufacture and design of carbon nanostructure based metal oxide nanostructures
for high-performance supercapacitor applications.