Photocatalysis is one of the techniques used for the eradication of organic pollutants from wastewater. In this study, Co–ZnO was tested as a photocatalyst for the degradation of methyl orange under irradiation of visible light. Co–ZnO loaded with 5%, 10%, and 15% Co was prepared by the precipitation method. The advanced techniques including X-ray diffraction, X-ray photoelectron spectroscopy, diffuse reflectance UV–visible spectroscopy, photoelectrochemical measurements, temperature-programmed desorption, photoluminescence, and fluorescence spectroscopy related to OH^• measurements were used for characterization of prepared Co–ZnO. Experiments showed that 10% Co–ZnO was a highly efficient catalyst for the photodegradation of methyl orange as compared to ZnO. The enhanced photocatalytic activity of Co–ZnO is attributed to the implantation of Co which inhibits the electron–hole recombination. A 100 mg/L solution of methyl orange dye was completely degraded within 130 min. The reaction kinetics has been described in terms of the Eley–Rideal mechanism.

Toxic antibiotic effluents and antibiotic-resistant bacteria constitute a threat to global health. So, scientists are investigating high-performance materials for antibiotic decomposition and antibacterial activities. In this novel research work, we have successfully designed ZIF-8@ZIF-67 nanocomposites via sol-gel and solvothermal approaches. The ZIF-8@ZIF-67 nanocomposite is characterized by various techniques that exhibit superior surface area enhancement, charge separation, and high light absorption performance. Yet, ZIF-8 has high adsorption rates and active sites, while ZIF-67 has larger pore volume and efficient adsorption and reaction capabilities, demonstrating that the ZIF-8@ZIF-67 nanocomposite outperforms pristine ZIF-8 and ZIF-67. Compared with pristine ZIF-8 and ZIF-67, the most active 6ZIF-67@ZIF-8 nanocomposite showed higher decomposition efficacy for ciprofloxacin (65%), levofloxacin (54%), and ofloxacin (48%). Scavenger experiments confirmed that ^•OH, ^•O^2-, and h⁺ are the most active species for the decomposition of ciprofloxacin (CIP), levofloxacin (LF), and ofloxacin (OFX), respectively. In addition, the 6ZIF-67/ZIF-8 nanocomposite suggested its potential applications in Escherichia coli for growth inhibition zone, antibacterial activity, and decreased viability. Moreover, the stability test and decomposition pathway of CIP, LF, and OFX were also proposed. Finally, our study aims to enhance the efficiency and stability of ZIF-8@ZIF-67 nanocomposite and potentially enable its applications in antibiotic decomposition, antibacterial activities, and environmental remediation.

Nanomaterials (NMs) have garnered significant attention in recent decades due to their versatile applications in a wide range of fields. Thanks to their tiny size, enhanced surface modifications, impressive volume-to-surface area ratio, magnetic properties, and customized optical dispersion. NMs experienced an incredible upsurge in biomedical applications including diagnostics, therapeutics, and drug delivery. This minireview will focus on notable examples of NMs that tackle important issues, demonstrating various aspects such as their design, synthesis, morphology, classification, and use in cutting-edge applications. Furthermore, we have classified and outlined the distinctive characteristics of the advanced NMs as nanoscale particles and hybrid NMs. Meanwhile, we emphasize the incredible potential of metal-organic frameworks (MOFs), a highly versatile group of NMs. These MOFs have gained recognition as promising candidates for a wide range of bio-applications, including bioimaging, biosensing, antiviral therapy, anticancer therapy, nanomedicines, theranostics, immunotherapy, photodynamic therapy, photothermal therapy, gene therapy, and drug delivery. Although advanced NMs have shown great potential in the biomedical field, their use in clinical applications is still limited by issues such as stability, cytotoxicity, biocompatibility, and health concerns. This review article provides a thorough analysis offering valuable insights for researchers investigating to explore new design, development, and expansion opportunities. Remarkably, we ponder the prospects of NMs and nanocomposites in conjunction with current technology.

This work incorporates a variety of conjugated donor-acceptor (DA) co-monomers such as 2,6-diaminopurine (DP) into the structure of a polymeric carbon nitride (PCN) backbone using a unique nanostructure co-polymerization strategy and examines its photocatalytic activity performance in the field of photocatalytic CO₂ reduction to CO and H₂ under visible light irradiation. The as-synthesized samples were successfully analyzed using different characterization methods to explain their electronic and optical properties, crystal phase, microstructure, and their morphology that influenced the performance due to the interactions between the PCN and the DPco-monomer. Based on the density functional theory (DFT) calculation result, pure PCN and CNU-DP_15.0 trimers (interpreted as incorporation of the co-monomer at two different positions) were extensively evaluated and exhibited remarkable structural optimization without the inclusion of any symmetry constraints (the non-modified sample derived from urea, named as CNU), and their optical and electronic properties were also manipulated to control occupation of their respective highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO). Also, co-polymerization of the donor–acceptor 2,6-diamino-purine co-monomer with PCN influenced the chemical affinities, polarities, and acid–base functions of the PCN, remarkably enhancing the photocatalytic activity for the production of CO and H₂ from CO₂ by 15.02-fold compared than that of the parental CNU, while also improving the selectivity.