Search Results (147)

A C/Zn-ZnO/TiO₂/Fe-Fe_xO_y (C/ZTF) nanocomposite photocatalyst with magnetic recoverability was synthesized by liquid-phase plasma (LPP) processing. Structural and surface analyses revealed that the photocatalyst consisted of TiO₂, Zn-ZnO, and Fe-Fe_xO_y domains integrated with a turbostratic-like carbon matrix and accompanied by defect-rich surface features. These structural characteristics are considered to support broader light absorption and more efficient interfacial charge migration. Under LED irradiation, C/ZTF achieved 95.8% degradation of methylene blue (MB) within 60 min at pH 7, while 92.5% degradation of tetracycline (TC) was achieved within 100 min at pH 9. Photoelectrochemical and photophysical analyses indicated that C/ZTF promoted charge separation and reduced carrier recombination more effectively than the individual component photocatalysts. Scavenger experiments suggested that •OH was the dominant reactive species in MB degradation, while •O₂⁻, h⁺, and e⁻ also contributed to the reaction. The enhanced photocatalytic performance of C/ZTF is associated with improved charge separation and interfacial charge-transfer behavior in the multicomponent heterostructure. The carbonaceous phase is considered to contribute to this process, and the overall photocatalytic behavior is discussed in relation to a dual Z-scheme-like pathway. These results provide design insight for recyclable multicomponent photocatalysts for environmental remediation. Full article

A Ce-doped photocatalytic composite with easy solid–liquid separation capability was prepared and a heterojunction was constructed between BiVO₄ and Fe₃O₄ via a co-precipitation method. A variety of characterization techniques were employed, such as X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), ultraviolet–visible spectroscopy (UV-vis), transmission electron microscopy (TEM) and energy-dispersive X-ray spectroscopy (EDS), as well as other related methods. Its photocatalytic performance for the degradation of Rhodamine B (RhB) was also studied. The results indicate that the photocatalytic efficiency of BiVO₄/Fe₃O₄ is 1.4 times that of the pure BiVO₄ matrix. In particular, the photocatalytic efficiency of Ce_1.5%-BiVO₄/Fe₃O₄ was 2.2 times higher than that of the pure BiVO₄ matrix, and a 100% degradation rate of RhB was achieved within 30 min. The introduction of Fe₃O₄ not only forms a heterojunction with BiVO₄, increasing the active sites and surface oxygen vacancies of the material and effectively suppressing the recombination of photogenerated electron (e^-)-hole (h⁺) pairs, but it also enables the rapid separation of the material from the wastewater solution by the magnetic properties of Fe₃O₄. Additionally, the partial substitution of Ce for Bi in the BiVO₄ lattice reduces the bandgap energy, which enhances the utilization efficiency of visible light and improves the photocatalytic performance of the composite material. The mechanism of RhB degradation by Ce_1.5%-BiVO₄/Fe₃O₄ composite materials is also analyzed in this study. Quenching experiments and EPR tests revealed that h⁺ and ${·\mathrm{O}}_2^{-}$ were the primary reactive species in the degradation process. Full article

A synergistic and magnetically recoverable NiFe₂O₄–MWCNT–CA nanocomposite was developed for efficient UV-driven photodegradation of hazardous organic pollutants. Biogenic NiFe₂O₄ nanoparticles synthesized using Costus speciosus extract exhibited a crystallite size of 32.5 nm, which increased to 83.6 nm upon incorporation into the MWCNT–cellulose acetate matrix. XRD confirmed the preservation of the cubic spinel structure, while VSM analysis showed maintained ferrimagnetic behavior with a saturation magnetization of 9.64 emu/g, enabling rapid magnetic separation. Although BET analysis revealed a reduction in surface area from 112.46 to 30.99 m²/g due to hybridization, the conductive MWCNT network significantly enhanced charge separation and interfacial electron transport. The composite displayed a widened optical bandgap of 5.3 eV, necessitating UV excitation for photocatalytic activity. Under UV irradiation, it achieved rapid degradation of methylene blue (97%) and Congo red (91%) at 20 mg/L, with corresponding rate constants of 0.119 and 0.076 min⁻¹. Scavenger experiments confirmed hydroxyl radicals (•OH) as the dominant reactive species, followed by photogenerated holes (h⁺). These results demonstrate a robust and synergistically engineered photocatalyst with high efficiency in removing organic pollutants under UV illumination. Full article

Recent advancements in nanotechnology and materials science have enabled the development of magnetic photocatalysts with improved efficiency, stability, and reusability, offering a promising approach for wastewater treatment. The integration of magnetic nanoparticles (MNPs) into photocatalytic processes has gained significant attention as a sustainable method for addressing emerging pollutants—such as antibiotics and pharmaceutical compounds—which pose environmental and public health risks, including the proliferation of antibiotic resistance. Surface modification techniques, specifically applied to MNPs, are employed to enhance their photocatalytic performance by improving surface reactivity, reducing nanoparticle agglomeration, and increasing photocatalytic activity under both visible and ultraviolet (UV) light irradiation. These modifications also facilitate the selective adsorption and degradation of target contaminants. Importantly, the modified nanoparticles retain their magnetic properties, allowing for facile separation and reuse in multiple treatment cycles via external magnetic fields. This review provides a comprehensive overview of recent developments in surface-modified MNPs for wastewater treatment, with a focus on their physicochemical properties, surface modification strategies, and effectiveness in the removal of antibiotics from aqueous environments. Furthermore, the review discusses advantages over conventional treatment methods, current limitations, and future research directions, emphasizing the potential of this technology for sustainable and efficient water purification. Full article

Photocatalytic degradation of organic molecules using TiO₂ has attracted attention in wastewater treatment because it can decompose organic compounds that are difficult to decompose by other methods. Meanwhile, efficient photocatalytic water treatment is difficult because it is not easy to separate nano-sized photocatalysts from water. In this review, we have described two approaches to solve the water separation challenge in the suspension type TiO₂ photocatalysts, which are uniformly distributed in water: magnetic TiO₂/SiO₂/Fe₃O₄ nanoparticles and TiO₂-polystyrene beads. The preparation, characterization, and photocatalytic performance of the two types of photocatalysts and their application are discussed. Finally, we compare two types of photocatalysts while focusing on the respective advantages and disadvantages of each, and the future direction of research. Full article

Photocatalytic water sterilization has emerged as a promising sustainable technology for addressing microbial contamination across diverse sectors including healthcare, food production, and environmental management. This review examines the fundamental mechanisms and recent advances in photocatalytic water sterilization, with a particular emphasis on the differential bactericidal pathways against Gram-negative and Gram-positive bacteria. Gram-negative bacteria undergo a two-step inactivation process involving initial outer membrane lipopolysaccharide (LPS) degradation followed by inner membrane disruption, whereas Gram-positive bacteria exhibit simpler kinetics due to direct oxidative attacks on their thick peptidoglycan layer. Escherichia coli has long been used as the gold standard in photocatalytic sterilization studies owing to its aerobic nature and suitability for the colony-counting method. In contrast, Lactobacillus casei, a facultative anaerobe, can be cultured statically and evaluated rapidly using turbidity-based optical density measurements. Therefore, both organisms serve complementary roles depending on the experimental objectives—E. coli for precise quantification and L. casei for rapid, practical assessments of Gram-positive bacterial inactivation under laboratory conditions. We also describe sterilization using light alone while comparing it to photocatalytic sterilization and then discuss two innovative suspension-based photocatalyst systems: polystyrene bead-supported TiO₂/SiO₂ composites offering balanced reactivity and separability and magnetic TiO₂-SiO₂/Fe₃O₄ nanoparticles enabling rapid magnetic recovery. Future research directions should prioritize enhancing visible-light efficiency using metal-doped TiO₂ such as Cu-doped systems; improving catalyst durability; developing new applications of photocatalysts, such as protecting RO membranes; and validating scalability across diverse industrial and medical water treatment applications. Full article

Alkaline treatment in 0.2 and 0.4 M NaOH solutions successfully generated controlled mesoporosity into ZSM-5 (Zeolite Socony Mobil-5) zeolite, resulting in average mesopore diameters of approximately 15 and 25 nm, respectively, while preserving the crystalline structure of the zeolite framework. Parent ZSM-5 and its mesoporous derivatives obtained by desilication were used to prepare (Fe species)@(zeolite matrix) composites. The synthesis was carried out by co-precipitating Fe²⁺/Fe³⁺ ions onto both parent and desilicated ZSM-5 matrices under oxygen-free conditions. Comprehensive characterization by X-ray diffraction, scanning electron microscopy, N₂ adsorption, vibrating-sample magnetometry, ⁵⁷Fe Mössbauer spectroscopy, and diffuse reflectance UV–Vis spectroscopy revealed that the degree of introduced mesoporosity dramatically influences the size, dispersion, phase composition, and oxidation state of the iron-containing nanospecies. On purely microporous ZSM-5, relatively large (~15 nm) partially oxidized magnetite nanoparticles are formed predominantly on the external surface, exhibiting superparamagnetism at room temperature (Mₛ = 11 emu/g) and a band gap of 2.12 eV. Increasing mesoporosity leads to progressively smaller and more highly dispersed iron(III) oxo/hydroxo clusters with significantly lower blocking temperatures and reduced magnetization (down to 0.7 emu/g for Fe@ZSM-5_0.4). All composites display strong visible-light absorption confirming their potential as magnetically separable visible-light-driven photocatalysts for environmental remediation. Full article

A Fe/CoFe₂O₄ nanocomposite was synthesized in one step by a hydrothermal method by processing the created iron and cobalt hydroxocomplexes. For precise characterization of the structure and morphology, X-ray diffraction (XRD), Fourier transform infrared spectroscopy, scanning electron microscopy, and ultraviolet–visible diffuse reflectance spectroscopy (UV-vis-DRS) were used. It was found that the obtained samples have a pronounced spinel crystalline structure, with the presence of metallic iron. The crystal size was determined by various methods and was 93–104 nm. The saturation magnetization, determined from the hysteresis loop, was 189.24 Emu/g, and the force coefficient was 602 Oe. UV-vis-DRS studies showed a band gap of 2.1 eV. The photocatalytic degradation of ibuprofen, streptocide, furacilin, methylene blue, and tetracycline was investigated under the influence of UV radiation in the presence of a photocatalyst. It was confirmed that the rate of degradation of pollutants obeys pseudo-first-order kinetics. Analysis of the constant rate of reactions showed that in order of decreasing stability, pharmaceutical drugs can be dissolved as follows: ibuprofen → streptocide → furatsilin → methylene blue → tetracycline. It was found that the ratio of photocatalyst and hydrogen peroxide concentrations is important for the destruction of more stable pollutants. The effect of hydrogen peroxide and catalyst concentrations is extremely strong. For unstable compounds, the most influential factor is the duration of treatment. Full article

The development of advanced photocatalysts that are efficient, recyclable and sustainable represents a significant challenge in the face of the growing presence of persistent organic contaminants in industrial wastewaters. This paper presents a novel approach based on the design of new heterostructures synthesized from BiOI and magnetic materials, using not only synthetic magnetite, but also magnetic compounds extracted from mine tailings, transforming environmental liabilities in active supporting materials through valorization strategies in line with the circular economy. Through precise control of composition, it was established that a proportion of 6% by mass of the magnetic phase allows the formation of a heterostructure that is highly photocatalytically efficient. These compounds were evaluated using caffeic acid, an organic contaminant of agroindustrial origin, as a target compound. Experiments were carried out under simulated solar radiation for 120 min. Among the materials synthesized, the BiOI/MMA heterostructure, derived from industrial tailing A, displayed an outstanding photodegradation efficiency of over 89.4 ± 0.25%, attributed to an effective separation of photoinduced charges, a broad active surface and a synergic interface interaction between its constituent phases. Furthermore, BiOI/MMA exhibited excellent structural stability and magnetic recovery capacity, which allowed for its reuse through two consecutive cycles without any significant losses to its photocatalytic performance. Thus, this study constitutes a significant contribution to the design of functional photocatalysts derived from industrial tailings, thus promoting clean, technological solutions for the treatment of wastewater and reinforcing the link between environmental remediation and circular economy. Full article

Zinc oxide (ZnO), a wide-bandgap semiconductor, has garnered significant interest for photocatalytic applications due to its excellent chemical stability, non-toxicity, and strong oxidative capability. In this study, density functional theory (DFT) calculations were employed to explore the impact of ruthenium (Ru) doping on the structural, electronic, and magnetic properties of wurtzite ZnO. The introduction of Ru leads to bandgap narrowing and the emergence of impurity states, thereby enhancing visible light absorption. Charge density analysis reveals enhanced electron delocalization, while the projected density of states (PDOS) indicates strong hybridization between the Ru 4d orbitals and the ZnO electronic states. The density of states at the Fermi level, N(EF), exhibits a notable dependence on doping concentration and magnetic configuration. For non-magnetic states, N(EF) reaches 11 states/eV and 9.5 states/eV at 12.5% and 25% Ru concentrations, respectively. In ferromagnetic configurations, these values decrease to 0.65 states/eV and 1.955 states/eV, while antiferromagnetic states yield 4.945 states/eV and 0.65 states/eV. These variations highlight Ru’s crucial role in regulating electronic density, thereby affecting electrical conductivity, magnetic properties, and photocatalytic efficiency. The results offer theoretical guidance for designing high-performance Ru-doped ZnO photocatalysts. Full article

Magnetically separable TiO₂-based composite photocatalysts have gained significant interest in the past two decades; however, the optimization of their synthesis and the stabilization of the magnetic iron oxide within the composite is still an open challenge. The present study investigates the photocatalytic behavior and recyclability of TiO₂-Fe₃O₄ composites, with emphasis on a possible correlation between pollutant degradation efficiency, recyclability, iron oxide stability, and the phase composition of the chosen TiO₂ base. Magnetite nanoparticles were synthesized under varied temperature and alkaline conditions to identify optimal parameters for achieving the desirable magnetic properties. The magnetic nanoparticles were integrated into composite systems with either commercial TiO₂ (Evonik Aeroxide P25 with anatase–rutile mixed phase) or a hydrothermally synthesized anatase TiO₂. The P25-based composite removed 99% paracetamol from aqueous solutions under UV-A irradiation and demonstrated successful recyclability, maintaining 96% paracetamol degradation efficiency after four uses. In contrast, the anatase TiO₂-based magnetic composite exhibited a lower performance (70%) and a significantly hindered recyclability (45% after four cycles). The difference in performance was attributed to variations in the phase composition of the employed TiO₂ in the composites and, consequently, in their charge separation mechanisms. Full article

Environmental pollution driven by socioeconomic development has intensified the need for advanced and sustainable wastewater treatment technologies. Herein, TiO₂-based photocatalysis emerged as a promising solution due to its oxidative potential, chemical stability, and eco-friendliness but does have unavoidable immobilized recoverability challenges. Therefore, this study explored the challenges and prospects of TiO₂-based photocatalysis for the degradation of emerging contaminants in wastewater. A comprehensive keyword analysis was conducted by using a decade of publications retrieved from Google Scholar, Scopus, and Web of Science (WOS) databases via Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) framework. From a pool of 518 refined publications, 318 significant keyword occurrences related to TiO₂-based photocatalysis advanced oxidation processes (AOPs) were revealed. The review delved into various types of AOP mechanisms and catalysts and highlighted the synergistic effect of process parameters and magnetization as recoverability potential for TiO₂-based photocatalysts. Furthermore, emerging strategies including surface modifications, doping, and hybrid AOP integrations were discussed to improve photocatalysis performance and industrial scalability. The study underscores the economic opportunity and environmental sustainability of degrading persistent organic pollutants by integrating a TiO₂-based photocatalytic system with a regenerative magnetic field into the water sector. Full article

Due to its persistence and potential negative effects on ecosystems and human health, microplastic pollution in aquatic environments has become a major worldwide concern. Photocatalytic degradation is a sustainable manner to degrade microplastics to non-toxic by-products. In this review, comprehensive discussion focuses on the synergistic effects of various photocatalytic materials including TiO₂, ZnO, WO₃, graphene oxide, and metal–organic frameworks for producing heterojunctions and involving multidimensional nanostructures. Such mechanisms can include the generation of reactive oxygen species and polymer chain scission, which can lead to microplastic breakdown and mineralization. The advancements of material modifications in the (nano)structure of photocatalysts, doping, and heterojunction formation methods to promote UV and visible light-driven photocatalytic activity is discussed in this paper. Reactor designs, operational parameters, and scalability for practical applications are also reviewed. Photocatalytic systems have shown a lot of development but are hampered by shortcomings which include a lack of complete mineralization and production of intermediary secondary products; variability in performance due to the fluctuation in the intensity of solar light, limited UV light, and environmental conditions such as weather and the diurnal cycle. Future research involving multifunctional, environmentally benign photocatalytic techniques—e.g., doped composites or composite-based catalysts that involve adsorption, photocatalysis, and magnetic retrieval—are proposed to focus on the mechanism of utilizing light effectively and the environmental safety, which are necessary for successful operational and industrial-scale remediation. Full article

This study employs density functional theory (DFT) to investigate the electronic and optical properties of molybdenum (Mo) and chalcogen (S, Se, Te) co-doped anatase TiO₂. Two co-doping configurations were examined: Model 1, where the dopants are adjacent, and Model 2, where the dopants are farther apart. The incorporation of Mo into anatase TiO₂ resulted in a significant bandgap reduction, lowering it from 3.22 eV (pure TiO₂) to range of 2.52–0.68 eV, depending on the specific doping model. The introduction of Mo-4d states below the conduction band led to a shift in the Fermi level from the top of the valence band to the bottom of the conduction band, confirming the n-type doping characteristics of Mo in TiO₂. Chalcogen doping introduced isolated electronic states from Te-5p, S-3p, and Se-4p located above the valence band maximum, further reducing the bandgap. Among the examined configurations, Mo–S co-doping in Model 1 exhibited most optimal structural stability structure with the fewer impurity states, enhancing photocatalytic efficiency by reducing charge recombination. With the exception of Mo–Te co-doping, all co-doped systems demonstrated strong oxidation power under visible light, making Mo-S and Mo-Se co-doped TiO₂ promising candidates for oxidation-driven photocatalysis. However, their limited reduction ability suggests they may be less suitable for water-splitting applications. The study also revealed that dopant positioning significantly influences charge transfer and optoelectronic properties. Model 1 favored localized electron density and weaker magnetization, while Model 2 exhibited delocalized charge density and stronger magnetization. These findings underscore the critical role of dopant arrangement in optimizing TiO₂-based photocatalysts for solar energy applications. Full article

The widespread contamination of aquatic environments by tetracycline antibiotics (TCs) poses a substantial threat to public health and ecosystem stability. Although photo-Fenton processes have demonstrated remarkable efficacy in degrading TCs, their practical application is limited by challenges associated with catalyst recyclability. This study reports the development of a novel magnetic recoverable SrFe₁₂O₁₉/g-C₃N₄ heterostructure photocatalyst synthesized via a facile one-step co-calcination method using industrial-grade precursors. Comprehensive characterization revealed that nitrogen defects and the formation of heterojunction structures significantly suppress electron (e⁻)–hole (h⁺) pair recombination, thereby markedly enhancing catalytic activity. The optimized 7-SFO/CN composite removes over 90% of oxytetracycline (OTC) within 60 min, achieving degradation rate constants of 0.0393 min⁻¹, which are 9.1 times higher than those of SrFe₁₂O₁₉ (0.0043 min⁻¹) and 4.2 times higher than those of g-C₃N₄ (0.0094 min⁻¹). The effectively separated e⁻ play three critical roles: (i) directly activating H₂O₂ to generate ·OH radicals, (ii) promoting the redox cycling of Fe²⁺/Fe³⁺ ions, and (iii) reducing dissolved oxygen to form ·O₂⁻ species. Concurrently, h⁺ directly oxidize OTC molecules through surface-mediated reactions. Furthermore, the 7-SFO/CN composite exhibits exceptional operational stability and applicability, offering a transformative approach for scalable photocatalytic water treatment systems. This work provides an effective strategy for designing efficient and recoverable photocatalysts for environmental remediation. Full article