The energy industry has been challenged by the current high population and high energy consumption, forcing the development of effective and efficient supercapacitor devices. The crucial issues until now have been high production cost, deprived cyclic stability, and squat energy density. To resolve these problems, various approaches have been taken, such as the development of long-life electrode materials with high capacity, rapid charging, and slow discharging to overcome poor life cycle stability. In the present work we focus on fabricating cost-effective unique-morphology, high-surface-area alpha-Co(OH)₂ for application in an aqueous-electrolyte symmetric supercapacitor. In this study, hierarchical nanoflakes assembled in three-dimensional (3D) flower-shaped cobalt hydroxide (HN-3DF-α-Co(OH)₂) electrode were synthesized using the solvothermal method with sodium dodecylbenzene sulfonate (SDBS) and methanol as solvents. Spectroscopic and microscopic techniques were used to characterize fabricated HN-3DF-Co(OH)₂, which revealed that the materials electrode exhibited the alpha phase with a hierarchical flower-like structure. A half-cell electrochemical assembly (three-electrode assemble cell) and symmetric full cell (two-electrode assemble cell) were examined in an aqueous electrolyte. In three-electrode assembly cells, HN-3DF-α-Co(OH)₂ exhibited 719.5 Fg^-1 specific capacitance (C_sp) at 1 Ag^-1 with excellent cyclic retention stability of approximately 88% after 3000 cycles. In two-electrode symmetric supercapacitive systems, HN-3DF-α-Co(OH)₂ achieved a maximum C_sp of 70.3 Fg^-1 at 0.4 Ag^-1 with the highest energy density of approximately 6.25 Wh/kg at a power density of 328.94 W/kg. The fabricated two-electrode assembly cell with the HN-3DF-α-Co(OH)₂ electrode retained cyclic stability of approximately 85% after 5000 repeated charge and discharge cycles. Solvothermally-synthesized, optimized HN-3DF-α-Co(OH)₂ showed outstanding electrochemical performance results in three- and two-electrode systems. This unique aqueous symmetric supercapacitor can be used to design cost-effective symmetric capacitors based on metal hydroxide.

In this work, silver (Ag) decorated reduced graphene oxide (rGO) coated with ultrafine CuO nanosheets (Ag-rGO@CuO) was prepared by the combination of a microwave-assisted hydrothermal route and a chemical methodology. The prepared Ag-rGO@CuO was characterized for its morphological features by field emission scanning electron microscopy and transmission electron microscopy while the structural characterization was performed by X-ray diffraction and Raman spectroscopy. Energy-dispersive X-ray analysis was undertaken to confirm the elemental composition. The electrochemical performance of prepared samples was studied by cyclic voltammetry and galvanostatic charge-discharge in a 2M KOH electrolyte solution. The CuO nanosheets provided excellent electrical conductivity and the rGO sheets provided a large surface area with good mesoporosity that increases electron and ion mobility during the redox process. Furthermore, the highly conductive Ag nanoparticles upon the rGO@CuO surface further enhanced electrochemical performance by providing extra channels for charge conduction. The ternary Ag-rGO@CuO nanocomposite shows a very high specific capacitance of 612.5 to 210 Fg⁻¹ compared against rGO@CuO which has a specific capacitance of 375 to 87.5 Fg⁻¹ and the CuO nanosheets with a specific capacitance of 113.75 to 87.5 Fg⁻¹ at current densities 0.5 and 7 Ag⁻¹, respectively.

The efficiency of zinc oxide (ZnO) nanoparticles for environmental decontamination is limited by their reliance on ultraviolet (UV) light and rapid charge carrier recombination. Carbon doping has been proposed to address these challenges by potentially enhancing visible light absorption and charge separation. This study aims to introduce a novel, single-step synthesis method for carbon-doped ZnO (C-Z) nanoparticles, leveraging the decomposition of zinc nitrate hexahydrate and furfural under a nitrogen atmosphere to improve photocatalytic activity under visible light. A series of C-Z variants (C-Z-1 to C-Z-5) and an undoped sample (ZnO-0) were synthesized. The influence of furfural on the synthesis process and doping mechanism was analyzed by X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and UV-visible diffuse reflectance spectroscopy (DRS). XPS confirmed the integration of carbon within the ZnO matrix, and XRD indicated increased lattice dimensions owing to doping. DRS revealed bandgap narrowing, suggesting enhanced charge separation. Among the variants, C-Z-3 significantly outperformed the others, showing a 12-fold increase in the photocatalytic degradation rate of Rhodamine B compared to undoped ZnO. The developed single-step synthesis method for C-Z nanoparticles represents a major advancement in materials engineering for ecological applications. The enhanced photocatalytic activity under visible light, as demonstrated by C-Z-3, underscores the potential of these nanoparticles for environmental decontamination.

The fabrication of energy storage electrode materials with high specific capacitance and rapid charge–discharge capability has become an essential and major issue of concern in recent years. In the present work, sphere-shaped interconnected interlinked binder-free nickel sulfide (NiS) grown on the surface of a three-dimensional nickel foam (3DNF) was fabricated by a one-step solvothermal method under optimized synthesis conditions, including different solvents, amounts of sulfur, and experimental reaction times. The fabricated binder-free SS-NiS@3DNF-E electrodes were characterized by a range of spectroscopic and microscopic techniques and further evaluated for their comparative electrochemical supercapacitive performance in half-cell assembly cells. The optimized sphere-shaped interconnected interlinked binder-free SS-NiS@3DNF-E-3 electrode showed an outstanding specific capacitance of 694.0 F/g compared to SS-NiS@3DNF-E-1 (188.0 F/g), SS-NiS@3DNF-E-2 (470.0 F/g), and SS-NiS@3DNF-E-4 (230.0 F/g) as well as excellent cycling stability up to 88% after 6700 continuous charge–discharge cycles, with an energy density of 24.9 Wh/kg at a power density of 250.93 W/kg. The obtained results demonstrate that the interconnected interlinked binder-free NiS@nickel electrode is a potential candidate for energy storage applications.