Dual Z-scheme core-shell PANI-CeO2-Fe2O3-NiO heterostructured nanocomposite for dyes remediation under sunlight and bacterial disinfection.

Nowadays, environmental pollution due to discharge of organic pollutants from food, textile, and pharmaceutical industries into clean water and development of contagious diseases due to pathogenic organisms provide impetus to material researcher to fabricate novel design for efficient photocatalyst and antimicrobial agents. In this regard, designing a core-shell heterojunction catalyst based on metal oxides is considered an auspicious approach. In present study, combating the problems of singular oxides, core-shell PANI-CeO2-Fe2O3-NiO nanocomposite (PCFN) and CeO2-Fe2O3-NiO nanocomposite (CFN) was synthesized through sol-gel and oxidative polymerization route with cetyletrimethylammonium bromide (CTAB) as surfactant. The XRD, FTIR, and Raman confirmed the formation of nanocomposites with core-shell morphology composed of PANI (shell) and oxides (Core) in PCFN with a particle size of 52 nm (TEM). Surprisingly, PCFN has lower band gap, e-/h+ recombination, and larger charge transfer character than CFN. The decomposition test using MB and MO dyes showed that PCFN degraded 99%, 98%, while CFN degraded only 73% and 54%, respectively, under 50 min sunlight illumination. The reusability was assessed up to 7th cycle for PCFN. The influence of operational parameters (catalyst dose, dye concentration, pH) was tested for PCFN. Further, the antimicrobial action against S. aureus (gram + ve), E. coli (gram -ve) were also tested. The supreme performance of PCFN has been credited to heterostructure dual Z-scheme formation and core-shell morphology supported with PANI, which suppresses the e-/h+ recombination process by promoting their separation. The present finding indicated that the PCFN is a promising modifier for bacterial disinfection and acts as a superb photocatalyst through core-shell formation with PANI support.

Sunlight-induced photocatalytic degradation of various dyes and bacterial inactivation using CuO-MgO-ZnO nanocomposite.

Novel tri-phase CuO-MgO-ZnO nanocomposite was prepared using the co-precipitation technique and investigated its physical properties using characterization techniques including XRD, FTIR, Raman, IV, UV-vis, PL, and SEM. The application of grown CuO-MgO-ZnO nanocomposite for the degradation of various dyes under sunlight and antibacterial activity against different bacteria were studied. The XRD confirmed the existence of diffraction peaks related to CuO (monoclinic), MgO (cubic), and ZnO (hexagonal) with CuO phase 40%, MgO 24%, and ZnO 36%. The optical energy gap of nanocomposite was 2.9 eV, which made it an efficient catalyst under sunlight. Raman and FTIR spectra have further confirmed the formation of the nanocomposite. SEM images revealed agglomerated rod-shaped morphology. EDX results showed the atomic percentage of a constituent element in this order Cu>Zn>Mg. PL results demonstrate the presence of intrinsic defects. The photocatalytic activity against methylene blue (MB), methyl orange (MO), rhodamine-B (RhB), cresol red (CR), and P-nitroaniline (P-Nitro) dyes has shown the excellent degradation efficiencies 88.5%, 93.5%, 75.9%, 98.8%, and 98.6% at 5 ppm dye concentration and 82.6%, 83.6%, 64.3%, 93.1%, and 94.3% at 10 ppm dye concentration in 100 min, respectively, under sunlight illumination. The higher degradation is due to the generation of superoxide and hydroxyl radicals. The recyclability test showed the reusability of catalyst up to the 5th cycle. The antibacterial activity against Escherichia coli, Klebsiella pneumoniae, Proteus Vulgaris, Staphylococcus aureus, and Pseudomonas aeruginosa bacteria with the zone of inhibition 30, 31, 30, 30, and 30 mm, respectively, was achieved.