Sol-gel dip-coating deposition was used to create Zr-doped Bi2O4 thin films with Zr in the range of 1-5 wt%. The monoclinic Bi2O4 phase was confirmed by an X-ray diffraction (XRD) analysis. After Zr doping in Bi2O4, there was a minor change in crystallite size and a reduction in the lattice parameters. UV-VIS-NIR spectrophotometry showed a decrease in the band gap of Bi2O4. These films were useful as absorbing layers for solar cells due to their decreased band gap, which allowed them to absorb a wide range of visible portions of the electromagnetic spectrum. SEM micrographs for each film showed an almost spherical-like appearance. The agglomeration of Bi2O4 into bigger particles with a lower surface area may be the cause of the decrease of the dielectric constant with an increase in Zr concentration. The AC conductivity of thin films increased with an increase in Zr concentration. Electrochemical charge-discharge test findings revealed the specific capacitance, power density, and energy of Zr-doped Bi2O4. Magnetic measurements of Zr-doped Bi2O4 nanostructures revealed ferromagnetic ordering at the surrounding temperature. The rise in saturation magnetization that occurred with an increase in Zr doping emerged from the formation of defects in the Bi2O4 lattice caused by oxygen vacancies and structural inhomogeneity, which promoted the growth of bound magnetic polarons. Additionally, Zr doping improved the photocatalytic qualities of Bi2O4. The enhanced photocatalytic activity of Zr-doped Bi2O4 nanoparticles was attributed to the higher UV-VIS light absorption and the reduced recombination rate of the photoinduced electron-hole pair making it a promising substance for water filtration. When Bi2O4 was combined with Zr, it inhibited the growth of Staphylococcus aureus (S. aureus), which was gram-positive while, Klebsiella pneumoniae (K. pneumoniae), Pseudomonas aeruginosa (P. aeruginosa) and Escherichia coli (E. coli) were gram-negative bacterial stains. Zr doping in Bi2O4 improved its antibacterial action.
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