Porous carbon materials (specific area over 2400 m² g⁻¹) were obtained from birch wood chips, the waste of its thermochemical processing water-insoluble lignocellulosic pyrolysis tar, and their mixture, by thermochemical activation with NaOH at 800 °C. Raw materials were carbonized by two methods: pyrolysis (500 °C) and hydrothermal (250 °C) treatment. The elemental and chemical composition of precursors and the effect of these parameters on the obtained carbon materials’ structure and porosity were studied. Results of the study showed that the carbonization method has little effect on the activated carbons’ specific surface area values; however, it allows for the regulation of pore size distribution.

Carbonization of biomass residues followed by activation has great potential to become a safe process for the production of various carbon materials for various applications. Demand for commercial use of biomass-based carbon materials is growing rapidly in advanced technologies, including in the energy sector, as catalysts, batteries and capacitor electrodes. In this study, carbon materials were synthesized from hardwood using two carbonization methods, followed by activation with H₃PO₄, KOH and NaOH and doping with nitrogen. Their chemical composition, porous structure, thermal stability and structural order of samples were studied. It was shown that, despite the differences, the synthesized carbon materials are active catalysts for oxygen reduction reactions. Among the investigated carbon materials, NaOH-activated samples exhibited the lowest Tafel slope values, of −90.6 and −88.0 mV dec^–1, which are very close to the values of commercial Pt/C at −86.6 mV dec^–1.

The goal of this research was to synthesize activated nitrogen-doped nanocarbons with high specific surface area and adjustable pore size distribution using wood charcoal as a raw material. The resulting carbon materials were tested for possible application as oxygen reduction reaction catalysts in alkaline media. Activated carbons were obtained using a thermochemical activation method with NaOH. Nitrogen was introduced into activated carbons using dicyandiamide solution. It was demonstrated that the content of introduced nitrogen depends on oxygen content in the structure of the activated carbon. The oxygen reduction reaction activity of the activated and nitrogen-doped carbon material was comparable with a commercial 20% Pt/C catalyst. Electrocatalytic properties of the synthesized N-doped wood-derived carbon catalysts may be associated with the highly developed surface area, specific ratio of micro- and mesopores, as well as the high percentage of pyridinic nitrogen.

Fuel cells, batteries and supercapacitors are critical to meet the rising global demand for clean, sustainable energy. Biomass-derived activated carbon can be obtained with tailored properties to fulfil the extensive need for low-cost, high-performance, catalyst and electrode materials. To investigate the possibility of nanoporous nitrogen-doped carbon materials as catalysts in fuel cells and electrodes in lithium-ion batteries, biomass precursors were thermochemically activated with NaOH at 800 °C, nitrogen was introduced using dicyandiamide and doping was performed at 800 °C. The chemical composition, porous structure, texture and electrochemical properties of the obtained materials change depending on the biomass precursor used. It has been found that the most promising precursor of the obtained materials is wood char, both as an oxygen reduction catalyst in fuel cells, which shows better properties than the commercial 20% Pt/C catalyst, and as an anode material in Li-ion batteries. However, catalysts based on black liquor and hybrid material have comparable properties with commercial 20% Pt/C catalyst and can be considered as a cheaper alternative.