posted on 2018-07-26, 00:00authored byChanderpratap Singh, Amit Paul
We report transformation
of a cost-effective nonporous carbon (<b>NC</b>) to an immense
microporous carbon (<b>IMC</b>) employing
a simple chemical activation route at 750 °C. N<sub>2</sub> adsorption/desorption
experiments revealed a remarkable increase in BET surface area (80–3030
m<sup>2</sup> g<sup>–1</sup>) for successor nanomaterial (<b>IMC</b>) in comparison to precursor nanomaterial (<b>NC</b>) 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<sup>–1</sup> at 0.5 A g<sup>–1</sup> current density) was observed in
2 M H<sub>2</sub>SO<sub>4</sub> using a three-electrode configuration.
Further, a massive specific capacitance of 1177 F g<sup>–1</sup> with a remarkable energy density of 163 Wh kg<sup>–1</sup> has been achieved by addition of hydroquinone in electrolyte with <b>IMC</b> (<b>IMC@H</b><sub><b>2</b></sub><b>Q)</b> 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 <b>IMC@H</b><sub><b>2</b></sub><b>Q</b> prevented chemical decomposition
of benzoquinone and thus also provided efficient routes for electron/proton
transport eluding annihilation of charge carriers.