In this work, different mass percent ratios of CoFe₂O₄ coupled g-C₃N₄ (w%-CoFe₂O₄/g-C₃N₄, CFO/CN) nanocomposites were integrated through a hydrothermal process for the sonocatalytic eradication of tetracycline hydrochloride (TCH) from aqueous media. The prepared sonocatalysts were subjected to various techniques to investigate their morphology, crystallinity, ultrasound wave capturing activity and charge conductivity. From the investigated activity of the composite materials, it has been registered that the best sonocatalytic degradation efficiency of 26.71 % in 10 min was delivered when the amount of CoFe₂O₄ was 25% in the nanocomposite. The delivered efficiency was higher than that of bare CoFe₂O₄ and g-C₃N₄. This enriched sonocatalytic efficiency was credited to the accelerated charge transfer and separation of e^--h⁺ pair through the S-scheme heterojunctional interface. The trapping experiments confirmed that all the three species i.e. ^•OH, h⁺ and ^•O₂^- were involved in the eradication of antibiotics. A strong interaction was shown up between CoFe₂O₄ and g-C₃N₄ in the FTIR study to support charge transfer as confirmed from the photoluminescence and photocurrent analysis of the samples. This work will provide an easy approach for fabricating highly efficient low-cost magnetic sonocatalysts for the eradication of hazardous materials present in our environment.

This work incorporates a variety of conjugated donor-acceptor (DA) co-monomers such as 2,6-diaminopurine (DP) into the structure of a polymeric carbon nitride (PCN) backbone using a unique nanostructure co-polymerization strategy and examines its photocatalytic activity performance in the field of photocatalytic CO₂ reduction to CO and H₂ under visible light irradiation. The as-synthesized samples were successfully analyzed using different characterization methods to explain their electronic and optical properties, crystal phase, microstructure, and their morphology that influenced the performance due to the interactions between the PCN and the DPco-monomer. Based on the density functional theory (DFT) calculation result, pure PCN and CNU-DP_15.0 trimers (interpreted as incorporation of the co-monomer at two different positions) were extensively evaluated and exhibited remarkable structural optimization without the inclusion of any symmetry constraints (the non-modified sample derived from urea, named as CNU), and their optical and electronic properties were also manipulated to control occupation of their respective highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO). Also, co-polymerization of the donor–acceptor 2,6-diamino-purine co-monomer with PCN influenced the chemical affinities, polarities, and acid–base functions of the PCN, remarkably enhancing the photocatalytic activity for the production of CO and H₂ from CO₂ by 15.02-fold compared than that of the parental CNU, while also improving the selectivity.

Amorphous CuO is considered as an excellent cocatalyst, owing to its large surface area and superior conductivity compared with its crystalline counterpart. The current work demonstrates a facile method to prepare amorphous CuO, which is grown on the surface of graphitic carbon nitride (g-C₃N₄) and is then applied for the photocatalytic degradation of tetracycline hydrochloride. The prepared CuO/g-C₃N₄ composite shows higher photocatalytic activities compared with bare g-C₃N₄. Efficient charge transfer between g-C₃N₄ and CuO is confirmed by the photocurrent response spectra and photoluminescence spectra. This work provides a facile approach to prepare low-cost composites for the photocatalytic degradation of antibiotics to safeguard the environment.

Sonocatalysis has attracted excellent research attention to eradicate hazardous pollutants from the environment effectively. This work synthesised an organic/inorganic hybrid composite catalyst by coupling Fe₃O₄@MIL-100(Fe) (FM) with ZnS nanoparticles using the solvothermal evaporation method. Remarkably, the composite material delivered significantly enhanced sonocatalytic efficiency for removing tetracycline (TC) antibiotics in the presence of H₂O₂ compared to bare ZnS nanoparticles. By adjusting different parameters such as TC concentration, catalyst dosage and H₂O₂ amount, the optimized composite (20 %Fe₃O₄@MIL-100(Fe)/ZnS) removed 78.25% antibiotic in 20 min at the cost of 1 mL of H₂O₂. These much superior activities are attributed to the efficient interface contact, effective charge transfer, accelerated transport capabilities and strong redox potential for the superior acoustic catalytic performance of FM/ZnS composite systems. Based on various characterization, free radical capture experiments and energy band structures, we proposed a mechanism for the sonocatalytic degradation of tetracycline based on S-scheme heterojunctions and Fenton like reactions. This work will provide an important reference for developing ZnS-based nanomaterials to study sonodegradation of pollutants.

In this work, ZnIn₂S₄/g-C₃N₄ (ZIS/CN) composites were synthesized by in-situ growth method, which showed excellent photocatalytic activity in the degradation of tetracycline and hydrogen production from water under visible light irradiation. ZnIn₂S₄ quantum dots (ZIS QDs) tightly combined with sheet g-C₃N₄ (CN) to accelerate the separation and transportation of photogenerated charges for enhanced photocatalytic activity. Among the prepared nanocomposites, 20%ZnIn₂S₄ QDs/g-C₃N₄ (20%ZIS/CN) delivered the highest photocatalytic activity. After 120 min of irradiation, the degradation rate of tetracycline with 20%ZIS/CN was 54.82%, 3.1 times that of CN while the rate of hydrogen production was 75.2 μmol·g⁻¹·h⁻¹. According to the optical and electrochemical characterization analysis, it was concluded that the excellent photocatalytic activities of the composite materials were mainly due to the following three points: enhancement in light absorption capacity, acceleration in the charge transport, and reduction in the carrier recombination rate through the formation of S-scheme heterojunction in the composite system. The high photocatalytic activity of ZIS/CN composites provides a new idea to develop highly efficient photocatalysts.