Search Results (4,069)

A homogeneous photocatalyst on a stable substrate is required for photocatalytic reactors in wastewater treatment. ZnO films were synthesized on stainless steel prepared by the spray pyrolysis technique at different deposition temperatures (350 to 500 °C in steps of 50 °C). Scanning electron microscopy showed microflowers formed by nanopetals with an average size of 2 μm. The ZnO wurtzite structure and its defects were studied by Raman spectroscopy, X-ray diffraction, diffuse reflectance, and photoluminescence spectroscopy. A deposition temperature of 400 °C was chosen due to the presence of a higher number of vibrational modes, better distribution of microflowers, smaller crystallite size and a higher number of defects than the other options. Lanthanides were incorporated into ZnO by solution spraying, and then thermal treatment was performed at 600 °C. The photocatalytic evaluation of ZnO showed the best photocatalytic activity under UV light at 365 nm with a 69.34% degradation efficiency at 120 min. Photocatalytic activity toward methylene blue degradation was enhanced in ZnO:Ce³⁺ (2 and 4 atom%) and ZnO:Nd³⁺ (0.05 and 2 atom%) samples, achieving degradation efficiencies above 90% within 30 min of UV–visible light irradiation. Full article

The synthetic industry has shortened human lifespans because of environmental contamination. Numerous physicochemical methods can be used to decompose the released organic contaminants, but heterogeneous photocatalysis stands out among them. The creation of a novel sunlight-active heterogeneous photocatalyst, ZVI@MnFe₂O₄/PTh, for possible degradation of RhB dye is discussed in this study. The nanocomposite was fabricated using the hydrothermal method and in situ polymerization of thiophene. The ternary composite photocatalyst (ZVI@MnFe₂O₄/PTh) and photocatalysts (ZVI@MnFe₂O₄ and MnFe₂O₄/PTh) were well characterized in terms of structure (Fourier transform infrared spectroscopy), morphology (scanning electron microscopy), composition (energy-dispersive X-ray), and crystallinity (X-ray diffraction). UV–visible spectroscopic analysis (Tauc plot) was used to determine the energy bandgaps of catalysts. The characterization study supports the successful assembly of ZVI@MnFe₂O₄ nanoparticles and polythiophene. To evaluate the photocatalytic performance, the photocatalytically helped degradation of Rhodamine B dye from wastewater was also investigated over the new catalysts. The designed heterojunction enhances photogenerated charge separation and stimulates the photocatalytic process. The proposed study’s findings demonstrated that the novel composite’s sunlight-active photocatalytic effectiveness (99% in 90 min at pH 4) was enhanced against the degradation of Rhodamine B dye. Different models were utilized to predict the reaction’s kinetics, and RSM was utilized as a statistical technique to examine the individual and then interaction effects of the influencing parameters. The RSM results were supported by the numerical values of the optimized parameters, which were pH = 4, H₂O₂ = 10 mM, and composite dose = 20 mg/50 mL, utilizing a 100 ppm RhB solution. Full article

Using bismuth oxide (Bi₂O₃) as the matrix and employing a doping modification strategy to introduce the rare-earth element La, this study prepared La/Bi₂O₃ visible-light-responsive photocatalysts with different doping ratios. The research systematically investigated the regulation mechanisms of La doping on the material’s phase structure, microstructure, band structure characteristics, and visible-light photocatalytic performance. The results indicate that an appropriate amount of La³⁺ equivalently substitutes Bi³⁺ in the lattice, inducing the complete transformation of pure α-Bi₂O₃ into the tetragonal β-Bi₂O₃ phase while maintaining the integrity of the crystal framework. Meanwhile, the modulation of the local electronic structure caused by La³⁺ substitution effectively narrows the bandgap width and broadens the visible-light response range; it also acts as an electron trap to significantly suppress the recombination of photo-generated electron–hole pairs, thereby enhancing charge transport efficiency. Visible-light catalytic degradation experiments confirmed that 4% La/Bi₂O₃ exhibits the optimal degradation kinetics for RhB, achieving a 72.88% degradation rate of Rhodamine B within 60 min of visible-light irradiation. The first-order reaction rate constant was 23 times that of pure Bi₂O₃, and the material demonstrated good stability under repeated cycles. Radical trapping experiments indicated that the order of contribution of active species was ·O₂⁻ > h⁺ > ·OH, with the superoxide radical (·O₂⁻) being the dominant active species. This study confirms that appropriate lattice doping with La can synergistically optimize the structure and optoelectronic properties of Bi₂O₃, providing experimental evidence and theoretical references for the rational design of highly efficient and stable visible-light-responsive Bi₂O₃-based photocatalytic materials. Full article

Adaptive feedback can destabilize a loop that would be stable under any fixed gain, so the speed at which the gain adapts is itself a design parameter. We study this effect in a minimal three-dimensional model motivated by the photocatalytic degradation of microplastics: a pollutant concentration is driven toward a setpoint by an ultraviolet (UV) actuator whose gain adapts online. The model has a single bilinear nonlinearity, so the local analysis can be carried out in closed form. Under an explicit feasibility condition, the system has a unique positive equilibrium. The Routh–Hurwitz criterion shows that this equilibrium is locally asymptotically stable below an explicit critical adaptation speed ${\kappa }_c$ and unstable above it. At $\kappa ={\kappa }_c$, a purely imaginary eigenvalue pair crosses the imaginary axis transversally, and a Hopf bifurcation occurs, with an explicit onset frequency. The first Lyapunov coefficient is computed in closed form; it separates a supercritical onset, for well-damped actuators, from a subcritical onset with hysteresis, for weakly damped actuators. Numerical experiments confirm the predicted limit cycle and the classification. All the stability results established here are local. Full article

The persistence of antibiotics like ciprofloxacin (CIP) in aquatic environments necessitates the development of efficient, low-cost wastewater treatment technologies. This study investigates a low-temperature fabrication strategy for mixed-phase copper oxide (CuO/Cu₂O) coatings synthesized via co-precipitation and immobilized using electrophoretic deposition (EPD). A critical finding was that a 25 min precursor aging time (T25) preserved a metastable mixture of CuO and Cu₂O phases, which is highly advantageous for creating heterojunction interfaces that enhance charge separation. In contrast, extended aging (T35) promoted phase consolidation toward bulk CuO, reducing catalytic surface area. During the EPD process, applied voltage acted as an influence to the relative phase composition and deposition behavior of the deposited coatings; 1.0 V was identified as the optimal condition, balancing high phase fidelity with enhanced crystallinity (average crystallite size of 30.6 nm) and mechanical stability. Photocatalytic experiments demonstrated significant CIP degradation, with the 0.9 V and 1.0 V films outperforming the 1.2 V film, possibly due to more favorable surface chemistry and phase diversity. While the 0.9 V film achieved the highest mineralization efficiency (18% TOC removal), the 1.0 V film offered the best balance between photocatalytic activity, structural stability, and phase selectivity for practical applications. High-Performance Liquid Chromatography-Mass Spectrometry HPLC-MS analysis suggested that degradation proceeds through oxidative pathways involving piperazine ring cleavage and defluorination. Full article

Organic pollutants in industrial wastewater present a severe threat to both the environment and human health. Photocatalytic technology, recognized for its eco-friendliness and high efficiency, has become a leading approach for degrading such pollutants. In this work, BiOCl nanosheets were first synthesized using a hydrothermal method. Subsequently, an anion exchange reaction with TAA in an oil bath generated a Bi₂S₃ intermediate layer on the BiOCl surface, followed by the in situ growth of ZIS nanostructures, successfully constructing a BiOCl@Bi₂S₃@ZIS double Z-scheme heterojunction. By adjusting the amount of BiOCl, the interface contact and dispersion of the heterojunction were optimized. Characterization results demonstrate that the BiOCl@ZIS-25 heterojunction possesses the highest specific surface area (103.5 m²·g⁻¹) and the most efficient charge separation. Under visible light irradiation, it achieved 97.88% degradation of methylene blue within 20 min, with a reaction rate constant 8 and 4 times higher than those of pure BiOCl and ZIS, respectively. Mechanistic investigations indicate that Bi₂S₃ interlayer acts as an electron-transfer bridge between BiOCl and ZIS, establishing a double Z-scheme charge transfer pathway that significantly enhanced the separation and utilization efficiency of photogenerated charge carriers. This study offers valuable insights for designing highly efficient and stable photocatalytic composite materials. Full article

Photocatalytic degradation technology has been widely acknowledged for its low cost and high degradation efficiency. However, the loss, migration and difficult recovery of powdered catalysts are still critical bottlenecks for practical applications. In this study, silver nanoparticles (Ag NPs)/polyvinylidene fluoride (PVDF) photocatalytic composite membranes were in situ fabricated by incorporating AgNO₃ into a PVDF casting solution, followed by electrospinning and UV post-treatment. The resulting membranes exhibited sustained photocatalytic capability towards dyes and antibiotics. The optimal membrane achieved 89.6% and 83.0% degradation efficiency for chloramphenicol (CAP) and rhodamine B within 16 h under UV irradiation, respectively. Free radical trapping experiments revealed that the superoxide radical (·O₂⁻) dominated the photocatalytic degradation of CAP, and the mechanism of photocatalytic degradation was explored. Additionally, the Ag NPs/PVDF photocatalytic membrane demonstrated a distinct antibacterial efficacy against Staphylococcus aureus (S. aureus) with a distinct inhibition zone of 20 mm, effectively inhibiting bacterial proliferation. Full article

The immobilization of photocatalysts onto biodegradable polymeric supports has emerged as an effective strategy to overcome catalyst recovery limitations associated with conventional slurry photocatalytic systems. In this study, chitosan/TiO₂ composite beads with different chitosan properties and TiO₂ loadings were synthesized and evaluated for the photocatalytic removal of Reactive Black 5 (RB5), a recalcitrant azo dye commonly encountered in textile wastewater. The effects of chitosan molecular weight, degree of deacetylation, and crosslinking treatment on the structural characteristics and photocatalytic performance of the composite beads were systematically investigated. The synthesized composites were characterized through physical property measurements, point of zero charge (pH_pzc) determination, and FTIR analyses. Photocatalytic performance was evaluated under various operational conditions, including pH, catalyst dosage, initial dye concentration, and temperature. Among the prepared materials, the crosslinked chitosan/TiO₂ composite bead produced from chitosan with an 85% degree of deacetylation exhibited the highest mineralization efficiency, achieving 76.23% total organic carbon (TOC) removal. FTIR analyses performed before and after treatment indicated that RB5 removal occurred through the combined effects of adsorption and photocatalytic oxidation. The effects of operational parameters revealed that acidic conditions significantly enhanced RB5 removal, while increasing temperature improved reaction kinetics and overall degradation efficiency. Kinetic studies indicated that the photocatalytic degradation process was best described by the pseudo-first-order kinetic model, with correlation coefficients ranging from 0.9841 to 0.9976. Arrhenius analysis yielded an apparent activation energy of 11.76 kJ mol⁻¹, indicating a low energy barrier for the degradation process. The results demonstrate that crosslinked chitosan/TiO₂ composite beads are promising, environmentally friendly, and sustainable photocatalytic materials for the treatment of dye-containing wastewater and advanced water purification applications. Full article

SrTiO₃/Nb₂O₅ composite materials with 1 and 10 wt.% Nb₂O₅ were prepared by a sol–gel route and characterized by XRD, Raman spectroscopy, SEM, BET, UV-Vis DRS, photoluminescence, and dielectric spectroscopy. The photocatalytic activity was evaluated via degradation of rhodamine B and tetracycline under UV and visible light. The addition of Nb₂O₅ resulted in a significant reduction in specific surface area (from 22.7 to 3.1 m²/g), a narrowing of the optical band gap (from 3.22 to 2.49 eV), and a decrease in photoluminescence intensity. Despite these changes, the photocatalytic performance decreased with increasing Nb₂O₅ content. For rhodamine B degradation, the UV rate constant fell from 0.0136 min⁻¹ for pristine SrTiO₃ to 0.0035 min⁻¹ for SrTiO₃/10% Nb₂O₅. The lower activity is mainly ascribed to the loss of active sites, surface carbonate formation, and enhanced non-radiative recombination at interface defects, which suppress charge transfer to the surface. The results demonstrate that careful control of the composite microstructure is essential for achieving efficient photocatalysis, even when heterojunction formation is thermodynamically favorable. Full article

The photocatalytic degradation of Acid Orange 7 (AO7) in aqueous solution in the presence of exfoliated C₃N₄ (n-C₃N₄) as a photocatalyst was investigated under simulated solar light irradiation. The n-C₃N₄ photocatalyst was synthesized by polymerization of urea as a precursor and characterized by UV/Vis and FTIR spectroscopy, and transmission electron microscopy. Degradation products were identified by high-performance liquid chromatography with high-resolution mass spectrometry (LC–HRMS). It was found that AO7 undergoes a series of oxidation steps mediated by radicals generated during light absorption by n-C₃N₄, as well as through a photosensitization process initiated by light absorption by AO7. This results in decolorization and the formation of aromatic and aliphatic intermediates, which undergo further oxidation to simpler compounds. Full article

The coordination chemistry of “salen-type” Schiff bases with the uranyl ion, trans-{U^VIO₂}²⁺, attracts the interest of several inorganic chemistry groups worldwide for a variety of reasons. The full synthetic investigation of the {UO₂}²⁺/H₂L reaction system, where H₂L is bis(2-hydroxyacetophenone)ethylenediamine, has provided access to complexes [UO₂(L)(EtOH)] (1) and [UO₂(L)(DMF)] (2) in moderate to good yields. The molecular structures of the two complexes are similar. The U^VI atoms are bonded to five oxygen and two nitrogen atoms in a distorted pentagonal bipyramidal geometry. The two uranyl oxo(or oxido) atoms occupy the axial positions, and the {O=U=O}²⁺ moiety is almost linear. The equatorial donor atoms are the two oxygens and the two nitrogens from the tetradentate chelating (1.1111 using Harris notation) L²⁻ ligand, and the oxygen atom of the coordinated solvent molecule. H-bonded dimers of 1 exist in its crystal structure. The complexes were fully studied in the solid state by IR, Raman, UV/Vis (diffuse reflectance) and emission spectroscopies, and the data are discussed in terms of the known structural data of the complexes and the coordination modes of the ligands. The structures of the complexes persist in solution as evidenced by NMR (¹H, ¹³C{¹H}) and UV/Vis spectroscopies, as well as by molar conductivity data. Complexes 1 and 2 exhibit moderate photocatalytic activity towards the degradation of the model organic dye methylene blue under continuous UV irradiation in aqueous media. The reaction kinetics were fitted using the Langmuir-Hinshelwood pseudo-first-order model. Combined IR and powder X-ray diffraction data show that the photocatalyst 1 remains unchanged after the photocatalytic experiment, whereas 2 undergoes DMF leaching. Based on literature reports, a simplified single-electron transfer mechanism has been proposed for the photocatalytic activity. Full article

Photocatalytic fuel cells (PFCs) integrate photocatalysis with fuel cell technology to enable simultaneous wastewater treatment and energy recovery. This review examines recent advances in PFC cathode materials, focusing on design strategies, reduction mechanisms, and applications. The cathode governs electron transfer and interfacial reactions, including oxygen reduction (4e⁻ or 2e⁻ pathways), direct pollutant electroreduction, and oxidant activation for radical generation. Cathodic materials including transition metal oxides/sulfides, carbon-based materials, metal–organic frameworks and their derivatives, are systematically summarized, evaluating their respective activities, stabilities and costs. Rational design via heterojunction engineering, defect modulation, and composite construction enables tunable reaction pathways and enhanced performance. Furthermore, representative applications are reviewed, with particular attention to the effective degradation of organic pollutants, and reduction of heavy metals and radionuclides in PFCs. Future efforts should prioritize long-term stability, scalable fabrication, and multi-functional cathode integration. Full article

The contamination of water bodies with organic pollutants has emerged as one of the most pressing environmental and public health challenges of the modern era. The continuous discharge of dyes, pesticides, agricultural runoff, and pharmaceutical residues into the aquatic ecosystem degrades water quality. Long-term exposure to these organic pollutants poses a severe risk to human and aquatic life. ZnO and TiO₂ have emerged as promising photocatalysts, particularly for degrading organic waste in wastewater. However, their photocatalytic activity is limited to the UV region due to their wide band gaps. To improve nanoparticle efficiency, polydopamine (PDA) is incorporated as a modifying agent. PDA-modified ZnO and TiO₂ nanocomposites exhibit enhanced photocatalytic activity in the degradation of various organic pollutants under visible light, compared with their unmodified counterparts. Furthermore, they exhibit improved antibacterial activity against a variety of waterborne pathogens; this is advantageous as wastewater contains both chemical pollutants and microorganisms. Thus, the combined photocatalytic and antibacterial properties of PDA-modified ZnO and TiO₂ make them promising materials for next-generation wastewater treatment. Full article

While silver halides (AgX) are promising visible-light photocatalysts for water remediation, their practical deployment is severely hindered by intrinsic photocorrosion, rapid charge recombination, and macroscopic recovery challenges. Here, we demonstrate a monolithic AgX/biomass carbon aerogel composite platform, constructed by anchoring AgX nanocrystals in situ onto a 3D hierarchical carbon skeleton. The carbon network not only suppresses nanoparticle aggregation but also plays contrasting optical roles: amplifying the intrinsic visible-light absorption of AgBr while endowing the otherwise UV-confined AgCl with substantial visible-light response. Consequently, the optimal 30 wt% AgBr/CA composite achieves a 95.68% methylene blue degradation efficiency within 60 min—outperforming pristine AgBr by 2.6-fold—while establishing robust activity against two additional, structurally distinct pollutants: rhodamine B and the colorless antibiotic ciprofloxacin. Notably, the free-standing monolith retains exceptional activity over six consecutive cycles. Mechanistic investigations reveal that the carbon aerogel functions as an electron-accepting reservoir, which accelerates interfacial charge separation and steers electron flow toward superoxide radical generation. Notably, XRD and XPS analyses confirm that no detectable metallic Ag⁰ is present in the as-prepared composites. This work establishes a sustainable and scalable architectural paradigm for designing highly efficient, stable, and easily recyclable photocatalytic systems. Full article

Synthetic azo dyes are the largest class of industrial colorants having widespread application in textile, food, cosmetic, and pharmaceutical industries. Moreover, they are persistent and toxic, threatening aquatic environments as well as human health. Disperse red 1 (DR1), a mono-azo dye belonging to the disperse dye group and widely used in polyester dyeing, cosmetics, and other applications, is of particular concern due to its mutagenic potential and resistance to conventional treatment processes. The present study investigated an integrated DR1 removal strategy using thermotolerant Bacillus licheniformis Tol1 as well as its EPS-stabilized biogenic silver nanoparticles (AgNPs). With a maximum tolerable concentration of 0.5 g L⁻¹, B. licheniformis Tol1 showed a maximum decolorization of 70.86% (0.2 g L⁻¹, 55 °C). However, response surface methodology (RSM) based on the Box–Behnken design showed an actual decolorization efficiency of 73.13%. The artificial neural network (ANN) model predicted an accuracy of R² = 0.9933, confirming the robustness and reliability of the experimental findings. To enhance dye removal efficiency, Tol1 EPS-stabilized AgNPs were synthesized via a green method and characterized using UV-Vis, SEM-EDAX, TEM, AFM, FTIR, DLS and zeta potential. Characterization of AgNP confirmed the formation of spherical stable AgNPs with an average size of 19.99 ± 0.38 nm, indicating polydisperse colloids nature with moderate electrostatic stability. A sunlight/H₂O₂-assisted process (photocatalytic experiments) demonstrated DR1 decolorization (80.72 ± 1.72% within 5 h under sunlight) following pseudo-first-order kinetics (k = 0.271 h⁻¹). Furthermore, FTIR analysis confirmed the degradation of the chemical structure of DR1 through the disappearance of the characteristic azo (–N=N–) bond, indicating cleavage of the dye molecule. Overall, the present study provides a dual biological–nanotechnological approach for DR1 decolorization using single bacteria as well as its polysaccharide-stabilized AgNP, a sustainable eco-friendly future approach. However, further studies on complete mineralization, transformation products, toxicity evaluation, detailed catalyst reusability, and silver (Ag) leaching are needed to facilitate the practical implementation for wastewater treatment. Full article