Considering the worldwide market of batteries and supercapacitors, the (partial or total) replacement of conventional fossil-derived carbonates with bio-based ones in electrolyte formulations would allow the production of safer and more sustainable devices. In this work, embracing the 7th principle of green chemistry, glycerol derivatives (namely glycerol carbonate and solketal carbonate) are tested as solvents and additives for electrolyte formulations. Glycerol carbonate is innovatively employed as promising electrolyte solvent for electric double-layer capacitors with excellent performances. On the other hand, a solketal carbonate-laden liquid electrolyte is investigated for potassium-based batteries, showing a rather stable electrochemical behaviour and performance close to those of commercial oil-derived alternatives.

Here, the hierarchical mesoporous-activated carbon particles obtained by KOH activation from pistachio shell wastes are modified by both the sulfonation process and CuO doping by hydrothermal heating (CuO@S-doped PSAC) for use as a supercapacitor. It is predicted that the electrochemical performance of the porous carbon electrode material obtained by such CuO doping and sulfonation process will be significantly increased with increased Faradaic capacitance. The electrochemical performance of CuO@S doped PSAC composite is systematically investigated by electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), and galvanostatic charge/discharge (GCD) in the presence of 1 M H2SO4, 1 M Na2SO4, and 1 M NaOH as electrolytes. The CuO@S doped PSAC-based electrode shows excellent stability with high specific capacitance up to 397.16 F/g at 0.1 A/g and 92.64% retention. Furthermore, FTIR, SEM, XRD, EDS, and nitrogen adsorption/desorption analyses are used for the characterisation of the obtained composites. Based on a significant supercapacitor performance, the synthesis strategy of carbon-based electrode material containing sulfonation and CuO modifications derived from agricultural biomass waste material is predicted to be a valuable example.

Herein, we report for the first time a simple strategy to design a hierarchical chemically exfoliated magnesium diboride and guar gum network structure decorated with Ru nanoparticles (eMgB2-GG@Ru) as an electrode to evaluate its electrochemical performance for the application of supercapacitor. The eMgB2 and functionalized eMgB2-GG@Ru materials were thoroughly examined using XRD, TGA, DLS, FE-SEM, STEM, AFM, XPS, and BET techniques. The combined eMgB2-GG@Ru electrode exhibits a network structure morphology with an increased interlayer distance of eMgB2 nanolayers along with a uniform distribution of spherical Ru nanoparticles. The electrochemical performance of eMgB2-GG@Ru and its pristine materials was studied through CV, GCD, and EIS to determine their supercapacitor performance. The eMgB2-GG@Ru electrode demonstrates higher specific capacitance (352 F/g) than its eMgB2@Ru (258.9 F/g), and MgB2 (214.5 F/g) counterparts at a current density of 0.5 A/g in a three-electrode setup using 3 M KOH electrolyte. The hierarchical eMgB2-GG@Ru solid-state symmetric devices maintained higher capacity retention of 89 % even after 7000 cycles, achieving a maximum energy density of 26.12 kW/kg at the power density of 450 W/kg at 0.5 A/g. Therefore, the innovative eMgB2-GG@Ru electrode offers superior electrochemical performance with efficient electrolyte ion mobility for energy storage applications.

Zinc Cobaltite (ZCO) and Nickel Oxide (NiO) nanoparticles (NPs) were synthesized using a sol-gel technique, and their composites with different weight ratios were prepared using a straightforward sonication method. The NiO and ZCO NPs had small crystallite size of 10 nm and 18 nm, respectively. According to the ultraviolet-visible (UV-Vis) spectra, pure NiO and ZCO NPs exhibited band gaps of ∼3.5 eV and 3.3 eV. Antibacterial activity against gram-positive (Staphylococcus aureus) and gram-negative (Escherichia coli) bacterial strains was also tested for the composite counterpart and its equivalents. Compared to pure NPs, the composite of 30 % ZCO-NiO (NZ3) had higher antibacterial activity with zone of inhibition of ∼13 mm against E. coli. The electrical and electrochemical properties were also explored and it was found that the composite of 50 % ZCO-NiO (NZ5) shows high specific capacitance of 188 F/g.

Two-dimensional nanosheets, with their distinct characteristics, are widely used in various applications such as water splitting, supercapacitors, catalysis etc. In this research, we produced Cu-BDC MOF nanosheets by using Cu2O nanotubes for metal ions and H2BDC as the organic linker. We combined these Cu-BDC MOF nanosheets with reduced graphene oxide (rGO) to form a nanocomposite. The collaboration between Cu-BDC MOF and rGO boosts both the catalytic reduction of 4-nitrophenol and the electrochemical capabilities. The conversion of 4-nitrophenol to 4-aminophenol is achieved using sodium borohydride as both a reducing agent and a catalyst. The study explores the impact of different concentrations of 4-nitrophenol and sodium borohydride on catalytic efficiency. The increase in sodium borohydride concentration enhances catalytic efficiency by providing more BH4- ions and electrons for the reduction process. The catalytic reduction process adheres to the Langmuir-Hinshelwood mechanism with apparent pseudo-first-order kinetics. Specifically, Cu-BDC MOF and rGO/Cu-BDC MOF exhibit specific capacities of 468.4 mA h/g and 656.4 mA h/g at a current density of 2 A/g, respectively, while also enhancing the operating voltage window. Therefore, electrodes based on rGO/Cu-BDC MOF nanosheets present a novel approach for environmental remediation and energy storage applications across various fields.

To improve the electrochemical performance of positive electrode materials, constructing graded nanostructures is a worthwhile approach. This study successfully synthesized nitrogen-doped graphene quantum dots (NGQD) modified (Ni0.5Co0.5)3V2O8 on a carbon nanotube (CNT) substrate to construct self-supporting electrodes for high-performance supercapacitors. The (Ni0.5Co0.5)3V2O8 nanosheets were successfully wrapped onto the CNT surface through a solution impregnation process, which increased the specific surface area and interlayer spacing of the material. Furthermore, the electrochemical properties of the electrode material underwent significant enhancement due to the synergistic interplay between metal ions and the numerous redox centers. The embedding of the NGQD enriched the materials with active sites and further improved its specific capacity without compromising the structure intergrity of the layer configuration. Using CNT as the substrate ensured the self-supporting nature of the electrode. Consequently, the (Ni0.5Co0.5)3V2O8/NGQD@CNT composite exhibits an ultra-high specific capacitance of 3018.2 F g-1 at 1 A g-1 and 2332 F g-1 at 10 A g-1. The asymmetric supercapacitor constructed with (Ni0.5Co0.5)3V2O8/NGQD@CNT and activated carbon (AC) presented an impressive energy density of 160.2 Wh kg-1 at a power density of 800 W kg-1. After 8000 charge-discharge cycles, the capacity retention rate was 78.5 %, with a Coulo mbic efficiency consistently above 98 %.

Two-dimensional covalent organic frameworks (COFs) are ideal electrode materials for electrochemical energy storage devices due to their unique structures and properties, and the accessibility and utilization efficiency of the redox-active sites within COFs are critical determinants of their pseudocapacitive performance. Via introducing meticulously designed phenolic hydroxyl (Ar-OH) groups with hydrogen-bond forming ability onto the imine COF skeletons, DHBD-Sb-COF exhibited improved hydrophilicity and crystallinity than the parent BD-Sb-COF, the redox-active sites (SbPh3 moieties) in COF electrodes could thus be highly accessed by aqueous electrolyte with a high active-site utilization of 93%. DHBD-Sb-COF//AC provided an excellent supercapacitive performance with an energy density of 78 Wh Kg-1 at the power density of 2553 W Kg-1 and super cycling stability, exceeding most of the previously reported pristine COF electrode-based supercapacitors. The \"two-in-one\" strategy of introducing hydroxyl groups onto imine COF skeletons to enhance both hydrophilicity and crystallinity provides a new avenue to improve the electrochemical performance of COF-based electrodes for high-performance supercapacitors.

This study describes the fabrication of composite electrodes comprising TiO2and reduced graphene oxide layers using a moderate-temperature hydrothermal method. The morphology, crystalline structure, chemical composition, and optical features of the prepared composites were analyzed by FE-SEM, x-ray diffraction, FTIR, and UV-visible spectroscopy. The cyclic voltammetry (CV) and Nyquist plots were used to assess the electrochemical and impedance responses of the composite electrodes, respectively. The analysis revealed that the incorporation of RGO reduced the TiO2bandgap to 3.87 eV 3.02 eV and improved the specific capacitance, enhancing the TiO2-RGO electrode\'s supercapacitive performance. CV studies highlight that the TiO2-RGO composite has a high specific capacitance of 152 F g-1at a substantially faster scan rate of 25 mV s-1in a 1.0 M-KOH dilute electrolyte. These findings confirmed the applicability of the fabricated electrodes as prospective supercapacitor electrodes.

Heterostructures and the introduction of heterogeneous elements have been regarded as effective strategies to promote electrochemical performance. Herein, sulfur species are introduced by a simple hydrothermal vulcanization method, which constructs the open heterostructure Fe7S8/Mn(OH)2 as a bifunctional material. The open cordyceps-like morphology can make the material contact more sufficiently with the electrolyte, exposing a large number of reaction sites. Furthermore, the introduction of the heterogeneous element S successfully constructs a heterogeneous interface, the interface-modulated composite material consists of Mn atoms contributing the main density of states (DOS) near the Fermi energy level from the density functional theory (DFT) calculations, which optimizes the adsorption energy of oxygen-containing intermediates during the oxygen evolution reaction (OER) process and reduces the reaction energy barrier, being conducive to the improvement of the material\'s electrochemical properties. As predicted, the Fe7S8/Mn(OH)2 material exhibits remarkable electrochemical properties, such as an overpotential of 202 mV at 10 mA cm-2 for the oxygen evolution reaction and even a specific capacitance of 2198 F g-1 at 1 A g-1. This work provides new insights into the role of introducing sulfur species and controlling the structure of the material, and exemplifies novel design ideas for developing bifunctional materials for energy storage and conversion.

Intensifying the synergy between confined carbon nanopores and ionic liquids (ILs) and a deep comprehension of the ion behavior is required for enhancing the capacitive storage performance. Despite many theoretical insights on the storage mechanism, experimental verification has remained lacking due to the intricate nature of pore texture. Here, a compressed micropore-rich carbon framework (CMCF) with tailored monolayer and bilayer confinement pores is synthesized, which exhibits a compatible ionophilic interface to accommodate the IL [EMIM][BF4]. By deploying in situ Raman spectroscopy, in situ Fourier-transform infrared spectroscopy, and solid-state nuclear magnetic resonance, the effect of the pore textures on ions storage behaviors is elucidated. A voltage-induced ion gradient filling process in these ionophilic pores is proposed, in which ion exchange and co-ion desorption dominate the charge storage process. Moreover, it is established that the monolayer confinement of ions enhances the capacity, and bilayer confinement facilitates the charging dynamics. This work may guide the design of nanoconfinement carbon for high-energy-density supercapacitors and deepen the understanding of the charge storage mechanism in ionophilic pores.