Metal oxide nanomaterials are one of the preferences as antibacterial active materials. Due to its distinctive electronic configuration and suitable properties, ZnO is one of the novel antibacterial active materials. Nowadays, researchers are making a serious effort to improve the antibacterial activities of ZnO by forming a composite with the same/different bandgap semiconductor materials and doping of ions. Applying capping agents such as polymers and plant extract that control the morphology and size of the nanomaterials and optimizing different conditions also enhance the antibacterial activity. Forming a nanocomposite and doping reduces the electron/hole recombination, increases the surface area to volume ratio, and also improves the stability towards dissolution and corrosion. The release of antimicrobial ions, electrostatic interaction, reactive oxygen species (ROS) generations are the crucial antibacterial activity mechanism. This review also presents a detailed discussion of the antibacterial activity improvement of ZnO by forming a composite, doping, and optimizing different conditions. The morphological analysis using scanning electron microscopy, field emission-scanning electron microscopy, field-emission transmission electron microscopy, fluorescence microscopy, and confocal microscopy can confirm the antibacterial activity and also supports for developing a satisfactory mechanism. Graphical Graphical abstract showing the metal oxides antibacterial mechanism and the fluorescence and scanning electron microscopic images.

Indigenous medicinal plant of Ethiopia has been applied for the first time to investigate the synergistic influence of phytoconstituents in green copper nanoparticles (g-Cu NPs) towards the enhancement of antimicrobial properties of NPs. We report the green synthesis of Cu NPs using Hagenia abyssinica (Brace) JF. Gmel. leaf extract. The synthesized g-Cu NPs were characterized by UV-visible, UV-DRS, FT-IR, XRD, SEM, EDXA, TEM, HRTEM, and SAED techniques. The maximum absorbance, λmax, was found to be 403 nm for g-Cu NPs due to surface plasmon resonance. The energy gap, Eg of NPs, was found to be 2.19 eV. FTIR spectra confirmed the presence of polyphenols, tannins, and glycosides in the leaf extract of Hagenia abyssinica. The spectral band at 740 cm^-1 is a characteristic of interaction between Cu and biomolecules of the extract. The XRD analysis revealed that the g-Cu NPs appears to be more crystalline in nature. SEM and TEM micrographs showed a mix of spherical, hexagonal, triangular, cylindrical, and irregularly shaped Cu particles. The average particle size of NPs was found to be 34.76 nm by ImageJ analysis. EDX analysis confirmed the presence of copper in the g-Cu NPs. In addition, the SAED pattern of g-Cu NPs presented concentric circular patterns for 4 major planes of crystalline copper and its oxides. The experimental and calculated d-spacing values of one of the crystal planes (111) were found to be 0.2432 nm and 0.2444 nm, respectively. The d-spacing values of 0.2444 nm and 0.2040 nm correspond to d₁₁₁Cu₂O and d₁₁₁Cu lattice fringes, respectively. The antibacterial test conducted on E. coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Bacillus subtilis showed good zone of inhibitions 12.7, 12.7, 14.7, and 14.2 mm, respectively, proving potentiality of g-Cu NPs as a remedy for infectious diseases caused by tested pathogens.

Even though the photocatalytic processes are a good technology for treatment of toxic organic pollutants, the majority of current photocatalysts cannot utilize sunlight sufficiently to realize the decomposition of these organic pollutants. As stated by various researchers, metal oxide nanoparticles have a significant photocatalytic performance under visible light source. Among various chemical and physical methods used to synthesize nanostructured silver oxide, green synthetic route is a cheaper and environmental friendly method. To confirm the optimum production of Ag₂O NPs, effect of pH, extract concentration, metal ion concentration, and contact time were optimized. The structure, morphology, crystallinity, size, purity, elemental composition, and optical properties of obtained Ag₂O NPs were characterized by different techniques, such as scanning electron microscopy (SEM), transmission electron microscope (HRTEM), X-ray diffraction (XRD), energy dispersive spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR), and UV-visible spectrophotometer accordingly as revealed by our literature review. The photocatalytic performance of the synthesized nanocrystalline Ag₂O by photocatalytic degradation of organic dyes under visible light irradiation has been discussed thoroughly in this review. Many past studies revealed that organic dyes and pollutants are decomposed completely by green synthesized Ag₂O NPs under irradiation of visible light.

Zinc oxide (ZnO) is a fascinating semiconductor material with many applications such as adsorption, photocatalysis, sensor, and antibacterial activities. By using a poly (vinyl alcohol) (PVA) polymer as a capping agent and metal oxides (iron and manganese) as a couple, the porous PVA-aided Zn/Fe/Mn ternary oxide nanocomposite material (PTMO-NCM) was synthesized. The thermal, optical, crystallinity, chemical bonding, porosity, morphological, charge transfer properties of the synthesized materials were confirmed by DTG/DSC, UV–Vis-DRS, XRD, FT-IR, BET, SEM-EDAX/TEM-HRTEM-SAED, and CV/EIS/amperometric analytical techniques, respectively. The PTMO-NCM showed an enhanced surface area and charge transfer capability, compared to ZnO. Using the XRD pattern and TEM image analysis, the crystalline size of the materials was confirmed to be in the nanometer range. The porosity and superior charge transfer capabilities of the PTMO-NCM were confirmed from the BET, HRTEM (IFFT)/SAED, and CV/EIS analysis. The adsorption kinetics (adsorption reaction/adsorption diffusion) and adsorption isotherm test confirmed the presence of a chemisorption type of adsorbate/methylene blue dye-adsorbent/PTMO-NCM interaction. The photocatalytic performance was tested on the Congo red and Acid Orange-8 dyes. The superior ascorbic acid sensing capability of the material was understood from CV and amperometric analysis. The noble antibacterial activities of the material were also confirmed on both gram-negative and gram-positive bacteria.

This work reveals a green combustion route for the synthesis of TiO₂, Fe₂O₃ and TiO₂-Fe₂O₃ nanocomposites as photocatalysts for decolorization of Titan Yellow (TY) and Methyl Orange (MO) dyes at room temperature in aqueous solution concentration of 20 ppm under UV-light irradiation. We observed that the TiO₂-Fe₂O₃ nanocomposite shows superior photocatalytic activity for TY dye compared to pure TiO₂ and Fe₂O₃. Rate constant (k) values of TiO₂, Fe₂O₃ and TiO₂–Fe₂O₃ for TY and MO are 0.0194, 0.0159, 0.04396 and 0.00931, 0.00772 0.0119 kmin⁻¹ respectively. The surface area and pore volume of TiO₂-Fe₂O₃ nanocomposite were found to be 71.56 m²/g and 0.076 cm³/g, respectively as revealed by BET studies. From the Barrett–Joyner–Halenda (BJH) plot, the mean pore diameter of TiO₂-Fe₂O₃ nanoparticles was found to be 2.43 nm. Further, the TiO₂-Fe₂O₃ nanocomposite showed good electrochemical behavior as an electrode material for supercapacitors when compared to pure TiO₂ and Fe₂O₃ nanoparticles resulted in stable electrochemical performance with nearly 100% coulombic efficiency at a scan rate of 10 mV/s for 1000 cycles. Interestingly, the novelty of this work is that the designed supercapacitors showed stable electrochemical performance even at 1000^th cycle, which might be useful for rechargeable supercapacitor applications. The electrochemical properties of the nanocomposites were compared by the data obtained by cyclic voltammograms, charge-discharge tests and electrochemical impedance spectroscopic studies. These results demonstrated that the TiO₂-Fe₂O₃ nanocomposite showed stable performance compared to TiO₂ and Fe₂O₃ nanoparticles at current density of 5 Ag⁻¹.

The NiO-CNT and NiO-Fe-CNT composites that have been prepared from waste high density polyethylene plastic and their carbon nanotube (CNT) quality-dependent supercapacitance tuning have been reported here. Multiwalled CNT (MWCNT) formation has been confirmed from TEM and Raman spectra with an I_D/I_G ratio of 0.77, which stands for high graphitization. The specific surface area (SSA) of MWCNTs in the NiO-Fe-CNT composite was 87.8 m²/g, while in the NiO-CNT composite, it was 25 m²/g. NiO-Fe-CNT displayed higher specific capacitance and energy density (1360 Fg^-1 and 1180 W h kg^-1) than NiO-CNT (1250 Fg^-1 and 1000 W h kg^-1), which may be due to the presence of higher-quality MWCNTs in the NiO-Fe-CNT composite. NiO-Fe-CNT displayed higher contributions of electric double-layer capacitor (59%) behavior compared to NiO-CNT (38%) and represented a hybrid supercapacitor. NiO-Fe-CNT also displayed a capacitive retention of 96% after 1000 charge-discharge cycles. Furthermore, studies in acidic electrolytes revealed higher performance of NiO-Fe-CNT than NiO-CNT, displaying specific capacitances of NiO-Fe-CNT to be 1147 Fg^-1 in 2 M H₂SO₄ and 943 Fg^-1 in 2 M HCl. It has been qualitatively explored that the quality of CNTs, SSA, and quantum confinement effects in the composites may be the factors responsible for the performance difference in NiO-Fe-CNT and NiO-CNT. The present work is geared toward the low-cost fabrication of high-quality CNT composites for supercapacitors and energy storage applications. The present work also contributes quantitatively to the understanding of CNT quality as an important parameter for the performance of CNT-composite-based supercapacitors.