Nitrogen-enriched hierarchically porous carbons (HPCs) were synthesized from a novel nitrile-functionalized benzoxazine based on benzoxazine chemistry using a soft-templating method and a potassium hydroxide (KOH) chemical activation method and used as electrode materials for supercapacitors. The textural and chemical properties could be easily tuned by adding a soft template and changing the activation temperature. The introduction of the soft-templating agent (surfactant F127) resulted in the formation of mesopores, which facilitated fast ionic diffusion and reduced the internal resistance. The micropores of HPCs were extensively developed by KOH activation to provide large electrochemical double-layer capacitance. As the activation temperature increased from 600 to 800 °C, the specific surface area of nitrogen-enriched carbons increased dramatically, micropores were enlarged, and more meso/macropores were developed, but the nitrogen and oxygen content decreased, which affected the electrochemical performance. The sample HPC-800 activated at 800 °C possesses a high specific surface area (1555.4 m(2) g(-1)), high oxygen (10.61 wt %) and nitrogen (3.64 wt %) contents, a hierarchical pore structure, a high graphitization degree, and good electrical conductivity. It shows great pseudocapacitance and the largest specific capacitance of 641.6 F g(-1) at a current density of 1 A g(-1) in a 6 mol L(-1) KOH aqueous electrolyte when measured in a three-electrode system. Furthermore, the HPC-800 electrode exhibits excellent rate capability (443.0 F g(-1) remained at 40 A g(-1)) and good cycling stability (94.3% capacitance retention over 5000 cycles).

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Template-free preparation of layer-stacked hierarchical porous carbons from cheap pitch precursors for high-performance all-solid-state supercapacitors.

Polyvinylidene fluoride homopolymer thin films have been prepared by the Langmuir-Blodgett technique, and their electrical properties have comprehensively been studied. The polyvinylidene fluoride homopolymer films show better ferroelectricity with higher polarization and higher breakdown electric field than that of the poly(vinylidene fluoride-trifluoroethylene) copolymer films. Inspection on the thickness dependence of the coercive field of the polyvinylidene fluoride films suggests an extrinsic polarization switching occurs in the thickness range from 200 to 45 nm, and a non-extrinsic switching is observed in the range between 45 and 11 nm, which is ascribed to the transition range from extrinsic to intrinsic switching.

Ozone associated with hydrogen peroxide as an advanced oxidation process had been employed to remove dibenzothiophene (DBT) in model oil in an ionic liquid (IL) system. DBT was oxidized availably by ozone and hydroxyl radicals that were generated by ozone and hydrogen peroxide. The oxidative productions of DBT were extracted to the IL phase because of their high polarity. The IL can be recycled 5 times without a significant decrease in desulfurization activity.

Nitrogen-rich porous carbons (NPCs) were synthesized from 1,5-dihydroxynaphthalene, urea, and formaldehyde based on benzoxazine chemistry by a soft-templating method with KOH chemical activation. They possess high surface areas of 856.8-1257.8 m(2) g(-1), a large pore volume of 0.15-0.65 cm(3) g(-1), tunable pore structure, high nitrogen content (5.21-5.32 wt%), and high char yields. The amount of the soft-templating agent F127 has multiple influences on the textural and chemical properties of the carbons, affecting the surface area and pore structure, impacting the compositions of nitrogen species and resulting in an improvement of the CO2 capture performance. At 1 bar, high CO2 uptake of 4.02 and 6.35 mmol g(-1) at 25 and 0 °C was achieved for the sample NPC-2 with a molar ratio of F127:urea = 0.010:1. This can be attributed to its well-developed micropore structure and abundant pyridinic nitrogen, pyrrolic nitrogen and pyridonic nitrogen functionalities. The sample NPC-2 also exhibits a remarkable selectivity for CO2/N2 separation and a fast adsorption/desorption rate and can be easily regenerated. This suggests that the polybenzoxazine-based NPCs are desirable for CO2 capture because of possessing a high micropore surface area, a large micropore volume, appropriate pore size distribution, and a large number of basic nitrogen functionalities.