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This paper reports the development of new ZnO/carbon xerogel composites (XZn w) for photocatalytic applications. The use of black wattle tannin as a precursor to the carbon xerogel aimed at reducing costs and environmental impacts. The composites were characterized by diffuse reflectance spectroscopy (DRS), BET surface area, scanning electron microscopy (FEG-SEM), X-ray photoelectron spectroscopy (XPS), energy dispersive spectroscopy (EDS), infrared spectroscopy (IR), and X-ray diffraction (XRD). The photocatalytic performance of the materials was evaluated in the decomposition process of methylene blue, a known toxic pollutant. The impacts of the catalyst dosage and calcination temperature on the photocatalytic process were also examined systematically. The X-ray profiles of the XZn w evidenced the existence of the hexagonal structure of the zinc oxide (wurtzite) in the composites. The XPS and XRD analyses confirmed the incorporation of carbon in the zinc oxide crystalline structure. The higher carbon content resulted in a larger surface area. All composites presented the ability to absorb radiation in less energetic wavelengths, contrary to pure zinc oxide that only absorbs radiation of wavelengths below 420 nm. The optimal dosage and calcination temperature were found to be 0.2 g L−1 and 300 °C. All the developed composites displayed significant photocatalytic activities in the decomposition of methylene blue under both visible and solar light. The composites had superior photocatalytic efficiency under visible light when compared to pure zinc oxide. The XZn 0.5 presented the best degradation efficiency under visible radiation. All materials presented similar photocatalytic responses under solar light, evidencing the synergy between the carbon xerogel and the zinc oxide. The photocatalytic mechanism was evaluated by trapping experiments to be mainly controlled by the electron vacancies that are generated during the photoexcitation of the composites.

This work explores the development of hybrid Nb2O5/carbon xerogel photocatalysts. The precursor materials used, such as tannin and recycled niobium scraps, enhance the economic and environmental aspects of the synthesis. The materials were characterized by diffuse reflectance spectroscopy, scanning electron microscopy, dispersive energy spectroscopy, infrared spectroscopy, Raman spectroscopy and X-ray diffraction. The photocatalytic action of the material was evaluated by methylene blue decomposition as determined by UV–visible spectroscopy. Anhydrous niobium oxide has a hexagonal structure. The X-ray profiles of the materials developed (XC-wNb) are similar to Nb2O5, confirming the presence of inorganic oxide in the matrix of these composites. The chemical elements that compose the samples are homogeneously distributed on the surface of the samples, confirming the dispersion of the oxide in the carbonaceous matrix. The XC-wNb absorbs radiation in a considerably wider range than inorganic oxides, in this case, for the entire wavelength range used in the experiments, thereby suggesting the synergistic effect of xerogel and niobium oxide on the optical properties of the XC-wNb samples. All XC-wNb presented photocatalytic activity under visible radiation, evidencing the beneficial coupling effect on the photocatalytic properties of the material. The XC-24Nb was the most effective photocatalyst at the wavelength used due its composition, morphological and photochemical properties. The methylene blue photodegradation is controlled to a greater extent by reaction with the OH • radical. The XC-24Nb also presents high stability and reusability, which are optimal properties for industrial application.