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Recently, the degradation of antibiotics has attracted a lot of attention all over the world, because the accumulation of these recalcitrant compounds in the environment, and their entry into the food chain have severely affected on human health. Herein, oxygen vacancy-rich CeO2 was decorated with Cu3BiS3 nanoparticles to fabricate Z-scheme CeO2-x/Cu3BiS3 photocatalysts with a simple procedure. Intriguingly, photocatalytic ability of CeO2-x/Cu3BiS3 (30%) nanocomposite in the detoxification of tetracycline hydrochloride, cephalexin, azithromycin, and rhodamine B was elevated 31.3, 28.2, 45.2, and 10.1-folds as much as CeO2, and 5.19, 5.97, 32.2, and 4.69-folds compared with the CeO2-x photocatalyst, respectively. The admirable activity of CeO2-x/Cu3BiS3 (30%) nanocomposite was ascribed to the production of many charge carriers, efficacious segregation and transfer of charges, and improved textural features, which were confirmed by UV-vis DRS, EIS, photocurrent density, PL, and BET analyses. In addition, the TC degradation pathway was investigated with LC-MS analysis, and also the biocompatibility of the purified solution was displayed with wheat seed cultivation. Regarding outstanding activity and facile synthesis, the CeO2-x/Cu3BiS3 (30%) photocatalyst could be utilized for wastewater treatment.

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RESUMEN

We demonstrated the photoredox catalytic performances of fluorescein derivatives, bearing heavy halogen atoms (Br or I) on a benzoic acid group, using photoinitiated free-radical polymerization. 4,5,6,7-Tetrabromofluorescein and 4,5,6,7-tetraiodofluorescein were used as visible-light-photoredox catalysts to initiate polymerization of poly(ethylene glycol) diacrylate and N-vinylpyrrolidone in the presence of triethanolamine under aerobic conditions. Their photocatalytic performances were evaluated by the hydrogelation of photopolymerization both on the surface of an agarose film and in a liquid solution. The polymerization degree increased considerably in the following order: tetraiodofluorescein

RESUMEN

Taking our current environmental situation in the world into consideration, people should face growing problems of air and water pollution. Heterogeneous photocatalysis is a highly promising tool to improve both air and water quality through decomposition/mineralization of contaminants directly into harmless CO2 and H2O under ambient conditions. In this contribution, we focused on the synthesis of self-assembly WO3 thin films via an electrochemical approach in the aqueous electrolyte containing fluoride ions toward air purification. The effect of preparation conditions such as applied potential (10-50 V), anodization time (15-120 min), concentration of H2SO4 (0.5-1.5 M) and NaF (0.1-1.0 wt.%) on the morphology, photocurrent response, and photocatalytic activity addressed to removal of air pollutant in the presence of as-prepared WO3 samples were thoroughly examined and presented. The results revealed the growth of nanoplatelets and their gradual transformation into flower-like structures. The oxide layers and platelet thickness of the WO3 samples were found to be proportionally related with the synthesis conditions. The photocatalytic ability toward air purification was evaluated by degradation of toluene from air mixture using low-powered LEDs as an irradiation source (λmax = 415 nm). The highest photoactivity was achieved in presence of the sample which possessed a well-ordered, regular shape and repeatable distribution of flower buds (100% of degradation). The results have confirmed that the oxide layer thickness of the anodic WO3 significantly affected the photocatalytic activity, which increased with the increasing thickness of WO3 (to 1.05 µm) and then had a downward trend. The photocurrent response evidenced that the well-organized sample had the highest ability in photocurrent generation under UV-Vis and Vis irradiation. Finally, a possible growth mechanism of WO3 NFs was also discussed.

RESUMEN

Vertically oriented, self-organized TiO2-MnO2 nanotube arrays were successfully obtained by one-step anodic oxidation of Ti-Mn alloys in an ethylene glycol-based electrolyte. The as-prepared samples were characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), UV-Vis absorption, photoluminescence spectroscopy, X-ray diffraction (XRD), and micro-Raman spectroscopy. The effect of the applied potential (30-50 V), manganese content in the alloy (5-15 wt. %) and water content in the electrolyte (2-10 vol. %) on the morphology and photocatalytic properties was investigated for the first time. The photoactivity was assessed in the toluene removal reaction under visible light, using low-powered LEDs as an irradiation source (λmax = 465 nm). Morphology analysis showed that samples consisted of auto-aligned nanotubes over the surface of the alloy, their dimensions were: diameter = 76-118 nm, length = 1.0-3.4 µm and wall thickness = 8-11 nm. It was found that the increase in the applied potential led to increase the dimensions while the increase in the content of manganese in the alloy brought to shorter nanotubes. Notably, all samples were photoactive under the influence of visible light and the highest degradation achieved after 60 min of irradiation was 43%. The excitation mechanism of TiO2-MnO2 NTs under visible light was presented, pointing out the importance of MnO2 species for the generation of e- and h⁺.

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