The presence of non-biodegradable, toxic, and harmful organic pollutants in various environmental mediums poses significant threats to ecosystems and human health. This study investigates the impact of transition metal (TM) doping on the photocatalytic performance of copper oxide nanoparticles (CuO NPs) in degrading methylene blue (MB) dye under sunlight irradiation. CuO NPs are synthesized using the co-precipitation method. X-ray diffraction (XRD) analysis revealed a monoclinic structure with space group C2/c for undoped and TM–doped CuONPs, with crystalline sizes ranging from 13 nm for undoped to 36 nm for Zn-doped CuO. Based on UV–Visible Spectroscopy data, the band gap energies and the nature of electronic band transitions are determined using a new simplified calculation method. Accordingly, direct band gap energy exhibits a slight red-shift as a result of doping with Ni, Mn or Fe, from 1.427 eV for undoped to 1.402 eV for Fe-doped CuO. While Co or Zn doping, induces a trivial blue-shift to 1.468 eV and 1.434 eV respectively. The CuO particles show a heterogenous distribution size and shape. The mean grain size raised from 34.3 nm for undoped to about 100 nm for TM-doped CuONPS, excluding the Co-doped CuO for which the mean grain size reached 154.532 nm with highest standard deviation heterogeneity of 125.737 nm. Furthermore, photocatalytic experiments demonstrated that TM-doping significantly enhanced the degradation rate of MB dye under sunlight irradiation. Co-doped CuO is the most efficient catalyst. This makes TM-doping a promising pathway for the use of CuO NPs in wastewater decontamination applications.
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