The impediments confronted by flexible batteries for
fabrication
methodologies and lower specific power for real-time applications
ameliorate the stand of flexible supercapacitors as a novel impartial
executor in the storage of energy. The commendable attributes of specific
energy, long-cycle stability, and rapid ion transport make supercapacitors
a crucial candidate in the devices of storage of energy. Eying on
these recompenses of supercapacitors, Ni4CuO5-mw-CNT and rGO-FeVO3 are fabricated for higher energy
asymmetric solid-state supercapacitors through a facile solvothermal
procedure delineated. The typical morphology of bimetallic oxides
with crystallinity variation depicts a high surface area that grossly
supersedes the sites of redox-active, which influences the diffusion
of electrolyte ions and the variable-valence redox reaction with ion
embolism. The synthesized oxide is investigated using X-ray diffraction,
X-ray photoelectron, and Raman spectroscopy to affirm the phase and
inspected by electron microscopy for structural features with BET.
The Hirshfeld surface simulation analysis assists in grasping the
electronic interaction to explicate the experimental consequences.
An asymmetric supercapacitor (ASC) device comprising Ni4CuO5-mw-CNT as a cathode and rGO-FeVO3 as an
anode is assembled. The electrochemical response of Ni4CuO5-mw-CNT and rGO-FeVO3 electrodes exhibits
higher specific capacitances of ∼778.8 and ∼478 F/g
at a current density of 0.4 A/g, respectively, superior long-cycle
stabilities, and rate capabilities. Moreover, the convened ASC device
achieves a maximum specific energy of ∼29.2 Wh/kg and a specific
power density of ∼3201.6 W/kg, along with a retention of the
capacitance of ∼82.6% after 10,000 cycles. The associated porous
morphology network affords instantaneous accessibility of the electrolytic
ions that utterly revamp the proficiency of the electrodes in the
field of energy storage.