In this study, we systematically study the efficient production method and electrochemical characteristics of activated carbons (AC) derived from rice husk (RH) and walnut shell (WS). In particular, the effectiveness of physical activation using carbon dioxide (CO₂) was investigated and compared with the more common chemical activation method using potassium hydroxide (KOH). The results show that the KOH–activated samples have remarkable specific capacities, reaching 157.8 F g⁻¹ for RH and 152 F g⁻¹ for WS at 1 A g⁻¹. However, the rate capability of AC obtained via KOH decreases significantly as the scanning rate increases, retaining only 51.5% and 68% of their original capacities for RH–KOH and WS–KOH, respectively, at 20 A g^–1. In contrast, CO₂–activated samples show a superior rate performance with a capacity retention of 75.6% for WS and 80% for RH at the same current density. In addition, electrochemical impedance spectroscopy (EIS) analysis shows that AC obtained via CO₂ has a lower charge transfer resistance compared to its KOH counterparts. CO₂–activated RH and WS electrodes show Rct values of 0.1 Ω and 0.24 Ω, respectively, indicating improved ion transport kinetics and surface area utilization. These results highlight the importance of activation techniques in tailoring the electrochemical behavior of biomass–derived carbon. This study not only expands the understanding of the interaction between activation, morphology, and performance but also indicates the potential of CO₂ activation as an environmentally friendly and efficient alternative. As the field of sustainable energy storage advances, this work provides valuable guidance for the development of high–performance supercapacitor electrodes with less environmental impact.

Biomass-based carbon nanofibers (CNF) were synthesized using lignin extracted from sawdust and polyacrylonitrile (PAN) (30:70) with the help of the electrospinning method and subsequent stabilization at 220 °C and carbonization at 800, 900, and 1000 °C. The synthesized CNFs were studied by scanning electron microscopy, energy-dispersive X-ray analysis, Raman spectroscopy, and the Brunauer–Emmett–Teller method. The temperature effect shows that CNF carbonized at 800 °C has excellent stability at different current densities and high capacitance. CNF 800 in the first test cycle at a current density of 100 mA/g shows an initial capacity of 798 mAh/g and an initial coulomb efficiency of 69.5%. The CNF 900 and 1000 show an initial capacity of 668 mAh/g and 594 mAh/g, and an initial Coulomb efficiency of 52% and 51%. With a long cycle (for 500 cycles), all three samples at a current density of 500 mA/g show stable cycling in different capacities (CNF 800 in the region of 300–400 mAh/g, CNF 900 and 1000 in the region of 100–200 mAh/g).

This study investigates the hydrogen adsorption performance of activated carbon (AC) derived from rice husks and modified with magnesium and nickel salts. Adsorption isotherms were recorded at 25 °C and 50 °C up to 80 bar, simulating practical storage conditions. The unmodified AC exhibited the highest hydrogen uptake (0.62 wt% at 25 °C), attributed to its high surface area and dominant ultramicroporosity (<0.9 nm). Modifications with Mg and Ni reduced adsorption capacity, likely due to partial pore blockage and decreased surface functionality, as confirmed by FTIR, Raman, and XRD analyses. Despite this, all samples demonstrated stable cyclic adsorption–desorption behavior and consistent isotherm profiles. Hysteresis observed in the modified samples suggests capillary condensation within mesopores. Thermodynamic analysis confirmed the exothermic nature of hydrogen adsorption. Among the modified materials, ACM10 (Mg-modified) exhibited the best performance (0.54 wt%), highlighting the importance of optimizing the metal content. The obtained results indicate that the micropore size distribution and accessible surface functionality critically govern the hydrogen storage capacity, suggesting that unmodified AC is a promising candidate for low-temperature hydrogen storage systems.

Hierarchical AC/Si/MXene composite anode integrates conductivity, porosity, and high capacity, ensuring stability and efficiency for next-generation lithium-ion batteries.

The article presents the results of comparative research on the physicochemical characteristics and catalytic activity of copper oxide supported on synthetic SiO₂ and SiO₂ (RH) from rice husk. SiO₂ (RH) is more hydrophobic compared to SiO₂, which leads to the concentration of copper oxide on its surface in the form of a “crust”, which is very important in the synthesis of low-percentage catalysts. According to SEM, XRD, and TPR-H₂, the use of SiO₂ (RH) as a carrier leads to an increase in the dispersion of copper oxide particles, which is the active center of ethanol dehydrogenation.