Copper oxide (CuO) nanoparticles (NPs) were decorated on reduced graphene oxide (rGO) through the effective synthetic route method. Powder X-ray diffraction, Fourier transform infrared, ultraviolet-visible absorption, and scanning electron microscopy techniques were used to analyze the chemical structure, functional groups, absorbance, and morphology. Under visible light illumination, the CuO/rGO nanocomposites have higher catalytic activity compared to the bare CuO NPs which were suitable for degradation of methylene blue (MB) and Congo red (CR) dyes. According to the findings, the CuO/rGO nanocomposites possess excellent photocatalytic efficiency. Thus, the synthesized CuO/rGO nanocomposite is a promising photocatalyst for the deterioration of organic pollutants in water and wastewater treatment.

Several different evaluation methods (EM) to obtain the band gap energy (E_g) of semiconductors via UV/Vis diffuse reflectance spectroscopy (DRS) are used in literature and no clear consensus which EM to use is established. By using P25 as a model semiconductor, evaluating 32 literature sources and our own experiments, we show that the determined E_g energy is heavily influenced by the EM (differences in E_g of up to 0.87 eV). For P25 loaded with CuO even contradictive effects of metal loading on the E_g are observed using different EM. Different phase compositions of TiO₂ are also shown to yield EM‐dependent results. This paper thus comprehensively investigates the most common EM on different relevant photocatalyst material classes, illustrates their mathematical and graphical determination, gives recommendations which method to use based on a quantitative indicator and illustrates common pitfalls in determining E_g via UV/Vis DRS.

Novel green bismuth oxybromide (BiOBr-G) nanoflowers were successfully synthesized via facile hydrolysis route using an Azadirachta indica (Neem plant) leaf extract and concurrently, without the leaf extract (BiOBr-C). The Azadirachta indica leaf extract was employed as a sensitizer and stabilizer for BiOBr-G, which significantly expanded the optical window and boosted the formation of photogenerated charge carriers and transfer over the BiOBr-G surface. The photocatalytic performance of both samples was investigated for the degradation of methyl orange (MO) and phenol (Ph) under the irradiation of visible light. The leaf extract mediated BiOBr-G photocatalyst displayed significantly higher photocatalytic activity when compared to BiOBr-C for the degradation of both pollutants. The degradation rate of MO and Ph by BiOBr-G was found to be nearly 23% and 16% more when compared to BiOBr-C under visible light irradiation, respectively. The substantial increase in the photocatalytic performance of BiOBr-G was ascribed to the multiple synergistic effects between the efficient solar energy harvesting, narrower band gap, high specific surface area, porosity, and effective charge separation. Furthermore, BiOBr-G displayed high stability for five cycles of photocatalytic activity, which endows its practical application as a green photocatalyst in the long run.