| dc.description.abstract | Graphene has superior properties which are enormously advantageous in energy
applications. Despite graphene’s superior properties, it has limitations such as the
utilization of complicated synthesis methods and restacking. One of the effective
strategies to overcome these limitations is the synthesis of graphene derivatives.
This study reports the synthesis of porous graphene (PG) via a novel one-step/onepot
electrochemical exfoliation approach. Electrochemical exfoliation was carried
out using a graphite rod and a stainless-steel electrode as the anode and cathode.
The electrolyte used was 0.1 M (NH4)2SO4 in 1 M H2SO4 and contained 0.03 M Phytic
acid (PA). As-synthesized PG was characterized using scanning electron microscopy
(SEM), X-ray diffraction (XRD), and Fourier transform infrared (FT-IR)
spectroscopy. SEM, FT-IR, and XRD confirmed the formation of a porous structure,
the formation of new bonds in PG, and the formation of graphene derivatives
respectively. The electrochemical characterization of materials for supercapacitor
applications was carried out using electrochemical impedance spectroscopy (EIS),
cyclic voltammetry (CV), and galvanostatic charge-discharge (GCD). EIS showed that
in PG, the resistance decreased, capacitance increased, and diffusion improved. CV
confirmed that PG produced the highest specific capacitance (SC) compared to
activated carbon (AC), graphite, and graphene. The percentage increments SC of
graphene and PG compared to graphite are 42280.7 % and 93346.5 % respectively.
GCD confirmed PG has low potential drop, resistance, and good charging time. These
results collectively provide strong evidence of easy synthesis of PG via onestep/
one-pot electrochemical exfoliation. | en_US |
