Over the past decades, the KOH-involved
activation has been established
to obtain porous carbons for supercapacitors. However, from the perspective
of economic efficiency and practicability, it is significant yet urgent
to explore a simple way to minimize the use of corrosive KOH for efficient
fabrication of supercapacitive carbons without sacrificing electrochemical
properties. Herein, we first develop a simple yet efficient activation
strategy from the inside out, where the KOH activator (∼40
wt %) is uniformly located in poly(vinyl alcohol) (PVA) hydrogel as
the precursor, to fabricate a three-dimensional hierarchically porous
carbon framework (denoted as PC-K). Compared with the porous carbon
obtained by physically mixing KOH and PVA, the PC-K with hydrophilic
surface is endowed with an even larger specific surface area, a higher
pore volume, and higher-content mesopores, ensuring abundant active
sites and rapid ion/electron transport. Such attractive merits result
in encouraging electrochemical capacitances of the PC-K electrode
with a loading of 5 mg cm–2 both in symmetric devices
and three-electrode systems with 6 M KOH and 1 M H2SO4 as aqueous electrolytes, which is particularly better than
other carbons synthesized with more KOH addition. More significantly,
the contribution here provides a guiding methodology for the feasible
commercial synthesis of advanced porous carbons toward next-generation
supercapacitors.