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Mechanisms of ion insertion in hard carbon and the corresponding structural impact on the graphene layer.

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Various electrochemical methods have been applied to establish the electrochemical characteristics of the electrical double layer capacitor consisting of the activated carbon material based electrodes and 1 M triethylmethylammonium tetrafluoroborate solution in acetonitrile and 1-ethyl-3-methylimidazolium tetrafluoroborate ionic liquid as the electrolytes. Activated carbon material used for the preparation of electrodes has been synthesized from hydrochar prepared via hydrothermal carbonization process of granulated white sugar solution in H2O, followed by activation with ZnCl2 with a mass ratio of 1:4 at the temperature 700°C. High porosity and Brunauer-Emmett-Teller specific surface area (SBET = 2100 m2 g−1), micropore surface area (Smicro = 2080 m2 g−1) and total pore volume (Vtot = 1.05 cm3 g−1) have been achieved for the granulated white sugar derived carbon (GWS carbon) material. Wide region of ideal polarizability (ΔE ≤ 3.0 V), short characteristic relaxation time (0.5 s and 4.0 s), high specific series capacitance (125 F g−1 and 140 F g−1) and high energy density (39 W h kg−1 and 48 W h kg−1) have been calculated for the GWS carbon material in 1 M triethylmethylammonium tetrafluoroborate solution in acetonitrile and 1-ethyl-3-methylimidazolium tetrafluoroborate ionic liquid, respectively, demonstrating that these systems are very promising for energy storage devices.

In this study, several peat-derived carbons (PDC) were synthesized using various carbonization protocols. It was found that depending on the carbonization method, carbons with very different surface morphologies, elemental compositions, porosities, and oxygen reduction reaction (ORR) activities were obtained. Five carbons were used as carbon supports to synthesize Co-N/PDC catalysts, and five different ORR catalysts were acquired. The surface analysis revealed that a higher nitrogen content, number of surface oxide defects, and higher specific surface area lead to higher ORR activity of the Co-N/PDC catalysts in acidic solution. The catalyst Co-N/C-2(ZnCl2), which was synthesized from ZnCl2-activated and pyrolyzed peat, showed the highest ORR activity in both rotating disk electrode and polymer electrolyte membrane fuel cell tests. A maximum power density value of 210 mW cm−2 has been obtained. The results of this study indicate that PDCs are promising candidates for the synthesis of active non-platinum group metal type catalysts.

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Using different carbonization protocols, five peat derived carbon materials were synthesized. These carbons have very different surface morphology confirmed by HR-SEM and different porosities and pore size distributions obtained by N2 sorption method. The ORR activity of the peat derived carbons also differs significantly in 0.1 M HClO4 solution. Additionally, co-doping the peat derived carbons with cobalt and nitrogen enhanced their catalytic activity considerably. The most active ORR catalyst was achieved using the carbon support where the dry milled peat was mixed with ZnCl2 and pyrolyzed in Ar for 2 h at 700 °C. Interestingly, the activity of the initial carbon powder does not seem to be a clear indicator of the final activity of the M-N/C catalysts synthesized from it.