In this work, nanosized Cu and Ni Schiff-base complexes, namely ahpvCu, ahpnbCu, and ahpvNi, incorporating imine ligands derived from the condensation of 2-amino-3-hydroxypyridine, with either 3-methoxysalicylaldehyde (ahpv) or 4-nitrobenzaldehyde (ahpnb), were synthesized using sonochemical approach. The structure and properties of the new ligands and their complexes with Ni(II) and Cu(II) were determined via infrared (IR), nuclear magnetic resonance (NMR), electronic spectra (UV-Vis), elemental analysis (CHN), thermal gravimetric analysis (TGA), molar conductivity (Λ_m), and magnetic moment (μ_eff). The combined results revealed the formation of 1:1 (metal: ligand) complexes for ahpvCu and ahpvNi and 1:2 for ahpnbCu. Additionally, CuO and NiO nanoparticles were prepared by calcination of the respective nanosized Cu/Ni complexes at 500 °C, and characterized by powder X-ray diffraction (XRD) and transmission electron microscopy (TEM). Significantly, the as-prepared nanosized Schiff-base Cu/Ni complexes and their oxides showed remarkable catalytic activity towards the selective oxidation of benzyl alcohol (BzOH) in aqueous H₂O₂/ dimethylsulfoxide (DMSO) solution. Thus, catalytic oxidation of BzOH to benzaldehyde (BzH) using both ahpvCu complex and CuO nanoparticles in H₂O₂/DMSO media at 70 °C for 2 h yielded 94% and 98% BzH, respectively, with 100% selectivity.

A series of copper-based systems containing two different nanocomposites (Cu₂O/CuO and Cu₂O/Cu) was synthesized by the egg white assisted auto-combustion route. This method was distinguished by the simplicity of its steps, low cost, one-pot synthesis process at low temperature and, short time. The characterization of the as prepared nanocomposites was carried out by using X-ray diffraction (XRD), Fourier-transform infrared (FTIR), Scanning electron microscope (SEM) and transmission electron micrograph (TEM), Energy dispersive spectrometry (EDS) techniques. Surface and magnetic properties of the obtained systems were determined by using N₂ adsorption/desorption isotherms at 77 K and the vibrating sample magnetometer (VSM) technique. XRD results confirmed the formation of Cu₂O/CuO and Cu₂O/Cu nanocomposites with different ratios of well crystalline CuO, Cu₂O, and Cu phases. FTIR results of the combusted product displays the presence of both CuO and Cu₂O, respectively. SEM/EDS and TEM results confirm the formation of a porous nanocomposite containing Cu, O, and C elements. The change in concentration of the oxygen vacancies at the surface or interface of both Cu₂O/CuO and Cu₂O/Cu nanoparticles resulted in different changes in their magnetization. Based on this study, it is possible to obtain nanocomposite-based copper with multiple valances by a simple and inexpensive route which can be suitable for the fabrication of different transition metal composites.

This work presents the fabrication of polymer electrolyte membranes (PEMs) that are made of polyvinyl alcohol-methylcellulose (PVA-MC) doped with various amounts of ammonium iodide (NH₄I). The structural and electrical properties of the polymer blend electrolyte were performed via the acquisition of Fourier Transform Infrared (FTIR) and electrical impedance spectroscopy (EIS), respectively. The interaction among the components of the electrolyte was confirmed via the FTIR approach. Electrical impedance spectroscopy (EIS) showed that the whole conductivity of complexes of PVA-MC was increased beyond the addition of NH₄I. The application of EEC modeling on experimental data of EIS was helpful to calculate the ion transport parameters and detect the circuit elements of the films. The sample containing 40 wt.% of NH₄I salt exhibited maximum ionic conductivity (7.01 × 10⁻⁸) S cm⁻¹ at room temperature. The conductivity behaviors were further emphasized from the dielectric study. The dielectric constant, ε’ and loss, ε’’ values were recorded at high values within the low-frequency region. The peak appearance of the dielectric relaxation analysis verified the non-Debye type of relaxation mechanism was clarified via the peak appearance of the dielectric relaxation. For further confirmation, the transference number measurement (TNM) of the PVA-MC-NH₄I electrolyte was analyzed in which ions were primarily entities for the charge transfer process. The linear sweep voltammetry (LSV) shows a relatively electrochemically stable electrolyte where the voltage was swept linearly up to 1.6 V. Finally, the sample with maximum conductivity, ion dominance of t_ion and relatively wide breakdown voltage were found to be 0.88 and 1.6 V, respectively. As the ions are the majority charge carrier, this polymer electrolyte could be considered as a promising candidate to be used in electrochemical energy storage devices for example electrochemical double-layer capacitor (EDLC) device.

A solution cast technique was utilized to create a plasticized biopolymer-based electrolyte system. The system was prepared from methylcellulose (MC) polymer as the hosting material and potassium iodide (KI) salt as the ionic source. The electrolyte produced with sufficient conductivity was evaluated in an electrochemical double-layer capacitor (EDLC). Electrolyte systems’ electrical, structural, and electrochemical properties have been examined using various electrochemical and FTIR spectroscopic techniques. From the electrochemical impedance spectroscopy (EIS), a maximum ionic conductivity of 5.14 × 10⁻⁴ S cm⁻¹ for the system with 50% plasticizer was recorded. From the EEC modeling, the ion transport parameters were evaluated. The extent of interaction between the components of the prepared electrolyte was investigated using Fourier transformed infrared spectroscopy (FTIR). For the electrolyte system (MC-KI-glycerol), the t_ion and electrochemical windows were 0.964 and 2.2 V, respectively. Another electrochemical property of electrolytes is transference number measurement (TNM), in which the ion predominantly responsibility was examined in an attempt to track the transport mechanism. The non-Faradaic nature of charge storing was proved from the absence of a redox peak in the cyclic voltammetry profile (CV). Several decisive parameters have been specified, such as specific capacitance (C_s), coulombic efficiency (η), energy density (E_d), and power density (P_d) at the first cycle, which were 68 F g⁻¹, 67%, 7.88 Wh kg⁻¹, and 1360 Wh kg⁻¹, respectively. Ultimately, during the 400th cycle, the series resistance ESR varied from 70 to 310 ohms.

A facile methodology system for synthesizing solid polymer electrolytes (SPEs) based on methylcellulose, dextran, lithium perchlorate (as ionic sources), and glycerol (such as a plasticizer) (MC:Dex:LiClO₄:Glycerol) has been implemented. Fourier transform infrared spectroscopy (FTIR) and two imperative electrochemical techniques, including linear sweep voltammetry (LSV) and electrical impedance spectroscopy (EIS), were performed on the films to analyze their structural and electrical properties. The FTIR spectra verify the interactions between the electrolyte components. Following this, a further calculation was performed to determine free ions (FI) and contact ion pairs (CIP) from the deconvolution of the peak associated with the anion. It is verified that the electrolyte containing the highest amount of glycerol plasticizer (MDLG3) has shown a maximum conductivity of 1.45 × 10⁻³ S cm⁻¹. Moreover, for other transport parameters, the mobility (μ), number density (n), and diffusion coefficient (D) of ions were enhanced effectively. The transference number measurement (TNM) of electrons (t_el) was 0.024 and 0.976 corresponding to ions (t_ion). One of the prepared samples (MDLG3) had 3.0 V as the voltage stability of the electrolyte.

One of the emerging and environmentally friendly technologies is the photoelectrochemical generation of green hydrogen; however, the cheap cost of production and the need for customizing photoelectrode properties are thought to be the main obstacles to the widespread adoption of this technology. The primary players in hydrogen production by photoelectrochemical (PEC) water splitting, which is becoming more common on a worldwide basis, are solar renewable energy and widely available metal oxide based PEC electrodes. This study attempts to prepare nanoparticulate and nanorod-arrayed films to better understand how nanomorphology can impact structural, optical, and PEC hydrogen production efficiency, as well as electrode stability. Chemical bath deposition (CBD) and spray pyrolysis are used to create ZnO nanostructured photoelectrodes. Various characterization methods are used to investigate morphologies, structures, elemental analysis, and optical characteristics. The crystallite size of the wurtzite hexagonal nanorod arrayed film was 100.8 nm for the (002) orientation, while the crystallite size of nanoparticulate ZnO was 42.1 nm for the favored (101) orientation. The lowest dislocation values for (101) nanoparticulate orientation and (002) nanorod orientation are 5.6 × 10⁻⁴ and 1.0 × 10⁻⁴ dislocation/nm², respectively. By changing the surface morphology from nanoparticulate to hexagonal nanorod arrangement, the band gap is decreased to 2.99 eV. Under white and monochromatic light irradiation, the PEC generation of H₂ is investigated using the proposed photoelectrodes. The solar-to-hydrogen conversion rate of ZnO nanorod-arrayed electrodes was 3.72% and 3.12%, respectively, under 390 and 405 nm monochromatic light, which is higher than previously reported values for other ZnO nanostructures. The output H₂ generation rates for white light and 390 nm monochromatic illuminations were 28.43 and 26.11 mmol.h⁻¹cm⁻², respectively. The nanorod-arrayed photoelectrode retains 96.6% of its original photocurrent after 10 reusability cycles, compared to 87.4% for the nanoparticulate ZnO photoelectrode. The computation of conversion efficiencies, H₂ output rates, Tafel slope, and corrosion current, as well as the application of low-cost design methods for the photoelectrodes, show how the nanorod-arrayed morphology offers low-cost, high-quality PEC performance and durability.