Abstract

The B/C/N composites were synthesized by a very simple method, that is, carbonization at HTT = 800–1200 °C of the precursor prepared by drying a solution mixture of polyacrylamide and boric acid, followed by boiling in water to remove borate by-products. The amount of insoluble B species in the composite increased linearly from 4.8 to 18.6 mass% with raising HTT. The XRD and FT-IR revealed that turbostratic h-BN started to form at around 1000 °C as a by-product. By XPS, major B and N components in the composite were B–N bond, C–B–O type B, pyridinic N, pyrrolic N, and quaternary N. A fraction for B–N bond including h-BN in the total B or N components increased with raising HTT and it exceeded 50 at% between 900 and 1000 °C. It was suggested that in the composites formed at HTT > 1000 °C the amounts of h-BN increased, leading to reduction in other B and N components. The S BET was almost unchanged up to 1000 °C, 410–420 m 2 g −1. Large and broad redox peaks arisen from plural reactions appeared in the cyclic voltammogram (CV) measured in 1 mol dm −3 H 2SO 4 for the composites formed at HTT ≤ 1000 °C. These peaks disappeared in 1 mol dm −3 solutions of Na 2SO 4 and Li 2SO 4. By comparing CV with that for C/N composite formed from PAA by the MgO template method, the pseudo-capacitance owing to reactions of B–N and C–B–O components with protons was found to be added to commonly observed pseudo-capacitance for nitrogen-doped carbons. The capacitances for the composites formed at 850–950 °C exceeded 300 F g −1 at 2 mV s −1 in the acid electrolyte and the retention at 50 mV s −1 was 78–80%. The shape of CV in the neutral electrolytes was trapezoid and the current density increased with lowering potential, suggesting adsorption and desorption of Na + and Li + ions. This was considered to be due to doped nitrogen, indicating the development of pseudo-capacitance. The capacitance per S BET was 0.33–0.74 F m −2 and 0.17–0.32 F m −2, larger for lower HTT, in the acid and neutral electrolytes, respectively.

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