The current work concentrated on the green synthesis of silver nanoparticles (AgNPs) through the use of aqueous Citruslimon zest extract, optimizing the different experimental factors required for the formation and stability of AgNPs. The preparation of nanoparticles was confirmed by the observation of the color change of the mixture of silver nitrate, after the addition of the plant extract, from yellow to a reddish-brown colloidal suspension and was established by detecting the surface plasmon resonance band at 535.5 nm, utilizing UV-Visible analysis. The optimum conditions were found to be 1 mM of silver nitrate concentration, a 1:9 ratio extract of the mixture, and a 4 h incubation period. Fourier transform infrared spectroscopy spectrum indicated that the phytochemicals compounds present in Citrus limon zest extract had a fundamental effect on the production of AgNPs as a bio-reducing agent. The morphology, size, and elemental composition of AgNPs were investigated by zeta potential (ZP), dynamic light scattering (DLS), SEM, EDX, X-ray diffraction (XRD), and transmission electron microscopy (TEM) analysis, which showed crystalline spherical silver nanoparticles. In addition, the antimicrobial and antioxidant properties of this bioactive silver nanoparticle were also investigated. The AgNPs showed excellent antibacterial activity against one Gram-negative pathogens bacteria, Escherichia coli, and one Gram-positive bacteria, Staphylococcus aureus, as well as antifungal activity against Candida albicans. The obtained results indicate that the antioxidant activity of this nanoparticle is significant. This bioactive silver nanoparticle can be used in biomedical and pharmacological fields.

The current study proposed a novel simple and environmentally friendly approach for producing silver nanoparticles (AgNPs) using an extract of Moringa oleifera leaves (MOL) and optimizing the different experimental factors required for the formation and stability of AgNPs. The formation of nanoparticles was confirmed by a color change from yellow to reddish-brown with a surface plasmon resonance band at 412 nm. The morphology, size, and elemental composition of AgNPs were investigated by zeta potential dynamic light scattering, field emission scanning electron microscopy, energy dispersive X-ray, X-ray diffraction, and transmission electron microscopy analysis, which showed crystalline and spherical AgNPs. The identification of functional groups was supported by Fourier-transform infrared spectroscopy. The photocatalytic activities of AgNPs were assessed in the degradation of organic Malachite green (MG) dye in the aqueous solution. Two kinetic adsorption models, the pseudo-first-order model and the pseudo-second-order model, and three isotherm models, the Langmuir, Freundlich, and Temkin, were used to mathematically characterize the MG degradation process. The pseudo-second-order kinetics and the Freundlich isotherm model were found to be in good agreement with the experimental data. As a result of their synergistic interaction with the MOL extract solution, the photocatalytic activity of AgNPs increases and they can successfully adapt to the photodegradation of organic dyes in industrial effluents.

This work reports the electrochemical fabrication of thin films comprising polyaniline nanofibers (PANI) in conjunction with graphene oxide (GO) and reduced graphene oxide (rGO) on ITO substrate, along with examining the electrochemical properties, with a focus on the influence of the substrate and electrolyte in the electrodeposition methods. The study explores the electrochemical characteristics of these thin films and establishes a flexible framework for their application in diverse sectors such as sensors, supercapacitors, and electronic devices. It analyzes the impact of the substrate and electrolyte in electrodeposition techniques. The effects were studied using techniques such as cyclic voltammetry and chronoamperometry. The fabrication process of PANI/GO and PANI/rGO thin films involved the integration of rGO within PANI via electropolymerization, conducted under sulfuric acid. GO was synthesized by modifying the well-known Hummers’ method and characterized by X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR). SEM showed the diameters of the formed PANI were between 40 and 150 nm, which helped to intertwine the rGO nanosheets with PANI nanofibers to form thin films. The electrochemical behavior of the PANI/rGO thin films was examined using cyclic voltammetry (CV) and chronoamperometry in different electrolytes, including sulfuric acid (H₂SO₄) and potassium nitrate (KNO₃). The CV profiles exhibited distinct oxidation and reduction peaks, with variations in the voltammogram morphology attributed to the nature of the electrolyte and the substrate employed during the electrodeposition process. These results highlight the critical role of both the substrate and electrolyte in governing the electrochemical performance of PANI/rGO thin films. The findings from this study demonstrate a versatile approach for the fabrication of PANI/graphene-based thin films with tunable electrochemical properties, and such a strategy has great application to fabricating other thin film composites for supercapacitors or other control source frameworks requiring enhanced charge storage and electrochemical responsiveness.

Due to its efficiency, eco-friendliness, non-toxicity, and cost-effectiveness, the utilisation of plant extracts in the manufacture of silver nanoparticles has garnered attention. The purpose of this study is to determine the feasibility of generating silver nanoparticles from an aqueous extract of Citrus limon leaves and their size and composition was characterized utilizing UV visible, FTIR, SEM, EDX, and Zeta seizer. Additionally, the antioxidant efficacy of Ag NPs was tested using the DPPH radical scavenging method, and their antibacterial activity was verified in vitro using the Agar well diffusion technique. Silver nanoparticles were successfully synthesized and exhibit surface plasmon resonance with an absorption maximum of 475.2 nm and the stabilization of the ions Ag to nanometric spherical negative charge particles, as verified by FTIR, MEB, EDX, and Zeta potential values. Furthermore, the silver nanoparticles created displayed a substantial bactericidal effect against the three types of bacteria (Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus) and an antifungal activity against (Candida albicans) as well as reasonable antioxidant properties.