Construction of flake ball-shaped Bi2WO6 embedded on phenyl functionalized g-C3N4 nanosheet for efficient degradation insight of colorless pollutants and its biological application.

A facile solvent-free solid-state method was adapted to synthesize the spherical-shaped Bi2WO6 engraved on phenyl-doped g-C3N4 nanosheet, i.e., Bi2WO6/Ph-gC3N4 (or BPCN) composites with varying weights of Bi2WO6. Several spectral analyses were used to characterize all the synthesized nanomaterials. The synthesized photocatalyst showed good absorption under visible light as confirmed by UV-visible DRS analysis. Morphological analyses like SEM and TEM determine the successful fabrication of binary heterocomposite. Further, the elements available in the fabricated binary nanocomposite were confirmed by XPS. The photocatalyst was used for the aerobic photocatalytic degradation of a few colorless pollutants like bisphenol A (BPA, 30 mg L-1), a microplastic constituent, and tetracycline (TC, 40 mg L-1), an antibiotic derivative to achieve the impressive results. The less intense PL signal obtained for the 20BPCN heterocomposite reveals the remarkable enhancement in e--h+ pair separation and recombination rate. The quenching study, alkaline terephthalic acid photoluminescence test (TA-PL), and NBT phototransformation study explain the formation of reactive species involved in the decomposition process. An oral cancer cell line (A-254) was tested for the anticancer activity analysis of the 20BPCN photocatalyst. Based on the obtained results, a Z-scheme electron transfer mechanism has been proposed for the photodegradation of model compounds.

Multifunctional electrospun nanofibrous scaffold enriched with alendronate and hydroxyapatite for balancing osteogenic and osteoclast activity to promote bone regeneration.

Electrospun composite nanofiber scaffolds are well known for their bone and tissue regeneration applications. This research is focused on the development of PVP and PVA nanofiber composite scaffolds enriched with hydroxyapatite (HA) nanoparticles and alendronate (ALN) using the electrospinning technique. The developed nanofiber scaffolds were investigated for their physicochemical as well as bone regeneration potential. The results obtained from particle size, zeta potential, SEM and EDX analysis of HA nanoparticles confirmed their successful fabrication. Further, SEM analysis verified nanofiber's diameters within 200-250 nm, while EDX analysis confirmed the successful incorporation of HA and ALN into the scaffolds. XRD and TGA analysis revealed the amorphous and thermally stable nature of the nanofiber composite scaffolds. Contact angle, FTIR analysis, Swelling and biodegradability studies revealed the hydrophilicity, chemical compatibility, suitable water uptake capacity and increased in-vitro degradation making it appropriate for tissue regeneration. The addition of HA into nanofiber scaffolds enhanced the physiochemical properties. Additionally, hemolysis cell viability, cell adhesion and proliferation by SEM as well as confocal microscopy and live/dead assay results demonstrated the non-toxic and biocompatibility behavior of nanofiber scaffolds. Alkaline phosphatase (ALP) and tartrate-resistant acid phosphatase (TRAP) assays demonstrated osteoblast promotion and osteoclast inhibition, respectively. These findings suggest that developed HA and ALN-loaded PVP/PVA-ALN-HA nanofiber composite scaffolds hold significant promise for bone regeneration applications.

Fabrication of Direct Z-Scheme CoNiWO4/Ph-gC3N4 Heterocomposites: Enhanced Photodegradation of Bisphenol A and Anticancer Activity.

Photocatalysis is realized by the design of a visible-light-active catalyst with robust redox capacity and broad absorption. In this study, a series of novel Z-scheme CoNiWO4/Ph-gC3N4 photocatalysts are synthesized to improve their redox property and photocatalytic activity toward broad visible light absorption. An intimate stable heterojunction is made between cobalt-nickel tungstate (CoNiWO4) and phenyl-doped graphitic carbon nitride (Ph-gC3N4), and its physicochemical properties are studied. The bifunctional properties of all of the synthesized materials were assessed by studying the decomposition of bisphenol A (BPA) and methyl orange (MO) dye as model pollutants, followed by an evaluation of their anticancer activity on human lung cancer cell lines. The photocatalyst with 20 wt % CoNiWO4 heterocomposite showed an enhanced response toward the removal of cancerous cells. The synthesized pristine CoNiWO4 and Ph-gC3N4 exhibit well-matched band structures and, hence, make it easier to create a Z-scheme heterocomposite. This may increase the lifetime of photoinduced charge carriers with a high redox power, thereby improving their photocatalytic and anticancer activity. An extensive analysis of the mechanism demonstrates that hydroxyl radicals (•OH) and superoxide radical anions (•O2-) are responsible for the degradation of organic compounds via Z-scheme charge transfer approach. These findings point toward a new route for creating effective Co-Ni tungstate-based direct Z-scheme photocatalysts for various redox processes, particularly the mineralization of resistant organic molecules.

Enhanced photodegradation of organic contaminants using V-ZnSQDs@TiO2 photocatalyst in an aqueous medium.

Vanadium-doped zinc sulfide quantum dots complexed with TiO2 have been designed using the sol-gel technique and characterized using analytical techniques, such as X-ray diffraction analysis (XRD), UV-Vis diffuse reflectance spectra (DRS), Fourier transforms Infra Red (FTIR), Brunauer-Emmett-Teller analysis (BET), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), and transmission electron microscopy (TEM). The X-ray diffraction analysis of the composite material showed sharp peaks corresponding to both TiO2 and ZnSQDs. The FTIR analysis exhibits a strong and broad absorption at 807 cm-1 indicating the assimilation of vanadium metal in the ZnSQDs lattice. The DRS spectra showed a bathochromic shift of 25 nm in the synthesized V-ZnSQDs@TiO2 composite compared with the pure sample. The photocatalytic performance of the synthesized composite was tested by studying the degradation of two different chromophoric organic dyes, rhodamine B (RhB), methylene blue (MB) and a drug derivative paracetamol (PCM) in aqueous suspension under UV-light illumination. Among the synthesized materials, the composite (V-ZnSQDs@TiO2) was established to be more active than the pure ZnSQDs, TiO2, and V-ZnSQDs for the degradation of compounds under investigation. The activity of the synthesized catalyst was also tested for the mineralization of all compounds by measuring the depletion in total organic carbon (TOC) at different irradiation times. The results showed that the catalyst degrades the compounds and mineralizes them efficiently. The primary reactive species involved in the photodegradation reaction were determined by quenching studies, terephthalic acid, and NBT probe methods. A probable mechanistic pathway for the decomposition of compounds has been proposed.