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).

Activated carbons (ACs) have been the most widespread carbon materials used in supercapacitors (SCs) due to their easy processing methods, good electrical conductivity, and abundant porosity. For the manufacture of electrodes, the obtained activated carbon based on sawdust (karagash and pine) was mixed with conductive carbon and polyvinylidene fluoride as a binder, in ratios of 75% activated carbon, 10% conductive carbon black, and 15% polyvinylidene fluoride (PVDF) in an N-methyl pyrrolidinone solution, to form a slurry and applied to a titanium foil. The total mass of each electrode was limited to vary from 2.0 to 4.0 mg. After that, the electrodes fitted with the separator and electrolyte solution were symmetrically assembled into sandwich-type cell construction. The carbon’s electrochemical properties were evaluated using cyclic voltammetry (CV) and galvanostatic charge–discharge (CGD) studies in a two-electrode cell in 6M KOH. The CV and CGD measurements were realized at different scan rates (5–160 mV s⁻¹) and current densities (0.1–2.0 A g⁻¹) in the potential window of 1 V. ACs from KOH activation showed a high specific capacitance of 202 F g⁻¹ for karagash sawdust and 161 F g⁻¹ for pine sawdust at low mass loading of 1.15 mg cm⁻² and scan rate of 5 mV s⁻¹ in cyclic voltammetry test and 193 and 159 F g⁻¹ at a gravimetric current density of 0.1 A g⁻¹ in the galvanostatic charge–discharge test. The specific discharge capacitance is 177 and 131 F g⁻¹ at a current density of 2 A g⁻¹. Even at a relatively high scan rate of 160 mV s⁻¹, a decent specific capacitance of 147 F g⁻¹ and 114 F g⁻¹ was obtained, leading to high energy densities of 26.0 and 22.1 W h kg⁻¹ based on averaged electrode mass. Surface properties and the porous structure of the ACs were studied by scanning electron microscopy, energy-dispersive X-ray analysis, Raman spectroscopy, and the Brunauer–Emmett–Teller method.

Carbon nanofibers based on lignin from wood waste have a promising potential for the ability to produce electrodes that can modernize existing energy storage technology. The most important detail is that the low cost, as well as the availability of the initial products for the production of lignin, will reduce the cost of energy storage devices and contribute to improving the environment. In this study, pine sawdust and elm sawdust were used as raw materials for the production of lignin, which accumulate in large quantities in metal workshops in Almaty. Lignin extraction was carried out using an organosolvent method, which is environmentally friendly, low-cost, uses minimal amounts of strong acids and metal catalysts, does not pollute water, and does not emit sulfur dioxide (SO₂). A comprehensive study of the characteristics of the obtained lignins from wood waste was carried out. Infrared spectroscopy (IR) revealed that the obtained lignin contains aromatic, phenolic, hydroxyl, methyl, and methoxyl groups. The results of nuclear magnetic resonance (NMR) spectroscopy showed the presence of a high number of syringyl (S) links compared to guaiacyl (G), which contribute to increased efficiency in the thermal processing of lignin. Also, this study investigated the use of the obtained lignins to produce continuous fibers by electrospinning. The effect of lignin mass on the viscosity of the lignin/polyacrylonitrile (PAN) solution and the effect of the carbonization temperature on the physico-chemical characteristics of the lignin/PAN solution were investigated. The following research methods were used for this purpose: Raman spectroscopy, thermogravimetric analysis (TGA), electron scanning microscopy, energy dispersion analysis, IR, NMR, and optical microscopy. The conditions for the production of lignin-containing carbon fibers at temperatures of 800, 900, and the carbonation heating rate, is an important parameter in the production of carbon fibers as it strongly affects the characteristics of the resulting carbon fibers. The heating rate affects were studied, and it was found that, at a heating rate of 5 °C/min and a carbonation temperature of 800 °C, porous carbon nanofibers with a diameter of 47 nm are formed in a nitrogen medium for 60 min.

Carbon fiber is known for being lightweight and adaptable, making it useful for various current and future applications. However, to broaden the use of carbon fibers beyond niche applications, production costs must be lowered. A potential approach to achieving this is by using more affordable raw materials, such as lignin, which is renewable, cost-effective, and widely available compared with the materials commonly used in industry today. This study explores the impact of metal ions on the quality of carbon fiber derived from lignin, focusing on its mechanical and electrochemical properties and morphology. The effect of a specific metal ion (Ni(NO₃)₂·6H₂O) was examined by incorporating it into the spinning solution. The carbonization stage of the fiber was conducted at temperatures of 800, 900, and 1000 °C in an inert atmosphere. Scanning electron microscopy (SEM) analysis showed no defects or damage in any of the fibers. Therefore, it was concluded that moderate concentrations of Ni²⁺ ions in the fibers do not influence the stabilization or carbonization processes, thus leaving the mechanical properties of the final carbon fiber unchanged. These carbon nanofibers were also tested as a sustainable alternative to the non-renewable materials used in electrodes for energy storage and conversion devices, such as supercapacitors. Electrochemical performance was assessed in a 6 M KOH solution using a two-electrode cell configuration. Galvanostatic charge–discharge tests were performed at different current densities (0.1, 0.25, 0.5, 1.0, and 2.0 A g⁻¹). The specific capacitance of the carbon nanofibers was determined from CVA data at various scan rates: 5, 10, 20, 40, 80, and 160 mV s⁻¹. The results indicated that at 0.1 A g⁻¹, the capacitance reached 108 F g⁻¹, and at a scan rate of 5 mV s⁻¹, it was 91 F g⁻¹. The innovation of this work lies in its use of lignin, a renewable and widely available material, to produce carbon fibers, reducing costs compared with traditional methods. Additionally, the incorporation of nickel ions enhances the electrochemical properties of the fibers for supercapacitor applications without compromising their mechanical performance.