posted on 2018-07-26, 00:00authored byChanderpratap Singh, Amit Paul
We report transformation
of a cost-effective nonporous carbon (NC) to an immense
microporous carbon (IMC) employing
a simple chemical activation route at 750 °C. N2 adsorption/desorption
experiments revealed a remarkable increase in BET surface area (80–3030
m2 g–1) for successor nanomaterial (IMC) in comparison to precursor nanomaterial (NC) presumably due to enhanced accessibility of reaction surface area
on carbon material for oxidants to react. In consequence, 250 times
specific capacitance enhancement (2.5–605 F g–1 at 0.5 A g–1 current density) was observed in
2 M H2SO4 using a three-electrode configuration.
Further, a massive specific capacitance of 1177 F g–1 with a remarkable energy density of 163 Wh kg–1 has been achieved by addition of hydroquinone in electrolyte with IMC (IMC@H2Q) employing a two-electrode configuration. Notably, a simple electrode
potential dependent chemical reversibility for hydroquinone redox
chemistry in the long term cyclic experiment (95% capacitance retention
after 5000 cycles) has been demonstrated wherein a strong electric
field helped to avoid agglomeration of hydroquinone molecules inside
the nanomaterial while hydrogen bond formation in IMC@H2Q prevented chemical decomposition
of benzoquinone and thus also provided efficient routes for electron/proton
transport eluding annihilation of charge carriers.