Search Results (132)

Commercially available bismuth subcarbonate (Bi₂O₂CO₃) was treated with nitric acid and the surfactant cetyltrimethylammonium bromide. The treated catalysts exhibited enhanced photocatalytic activity compared to pure Bi₂O₂CO₃ in the decolorization of rhodamine B (RhB) under visible light irradiation. The absorbance at 554 nm gradually decreased over time and disappeared completely within 80 min. The crystal structure, morphology, and optical properties of the samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-Vis diffuse reflectance spectroscopy (DRS), and photoluminescence (PL) spectroscopy. The improved photocatalytic activity of the treated catalysts was attributed to partial carbonate removal and the formation of Bi⁵⁺ species. Scavenger experiments indicated that superoxide radicals (·O₂⁻) and photogenerated holes (h⁺) played significant roles in the photocatalytic decolorization of RhB. Full article

Water pollution caused by increasing industrial and human activity remains a serious environmental challenge, especially due to the persistence of organic contaminants in aquatic systems. Photocatalysis offers a promising and eco-friendly solution, but in the case of bismuth oxide (Bi₂O₃) there is still a limited understanding of how structural and morphological features influence photocatalytic performance. In this work, a straightforward hydrothermal synthesis method followed by controlled calcination was developed to produce phase-pure α- and β-Bi₂O₃ with tunable morphologies. By varying the hydrothermal temperature and reaction time, distinct structures were successfully obtained, including flower-like, broccoli-like, and fused morphologies. XRD analyses showed that the final crystal phase depends solely on the calcination temperature, with β-Bi₂O₃ forming at 350 °C and α-Bi₂O₃ at 500 °C. SEM and BET analyses confirmed that morphology and surface area are strongly influenced by the hydrothermal conditions, with the flower-like β-Bi₂O₃ exhibiting the highest surface area. UV–Vis spectroscopy revealed that β-Bi₂O₃ also has a lower bandgap than its α counterpart, making it more responsive to visible light. Photocatalytic tests using Rhodamine B showed that the flower-like β-Bi₂O₃ achieved the highest degradation efficiency (81% in 4 h). Kinetic analysis followed pseudo-first-order behavior, and radical scavenging experiments identified hydroxyl radicals, superoxide radicals, and holes as key active species. The catalyst also demonstrated excellent stability and reusability. Additionally, Methyl Orange (MO), a more stable and persistent azo dye, was selected as a second model pollutant. The flower-like β-Bi₂O₃ catalyst achieved 73% degradation of MO at pH = 7 and complete removal under acidic conditions (pH = 2) in less than 3 h. These findings underscore the importance of both phase and morphology in designing high-performance Bi₂O₃ photocatalysts for environmental remediation. Full article

Over efficient photocatalysts, CO₂ photoreduction typically converts CO₂ into low-carbon chemicals, which serve as raw materials for downstream synthesis processes. Here, an efficient composite photocatalyst heterojunction (Cu₂O-u/g-C₃N₄) has been fabricated to reduce CO₂. Graphitic carbon nitride (g-C₃N₄) was synthesized via thermal polymerization of urea at 550 °C, while pre-dispersed Cu₂O derived from urea pyrolysis (Cu₂O-u) was prepared by thermal reduction of urea and CuCl₂·2H₂O at 180 °C. The heterojunction Cu₂O-u/g-C₃N₄ was subsequently constructed through hydrothermal treatment at 180 °C. This heterojunction exhibited a bandgap of 2.10 eV, with dual optical absorption edges at 485 nm and above 800 nm, enabling efficient harvesting of solar light. Under 175 W mercury lamp irradiation, the heterojunction catalyzed liquid-phase CO₂ photoreduction to formic acid, acetic acid, and methanol. Its formic acid production activity surpassed that of pristine g-C₃N₄ by 3.14-fold and TiO₂ by 8.72-fold. Reaction media, hole scavengers, and reaction duration modulated product selectivity. In acetonitrile/isopropanol systems, formic acid and acetic acid production reached 579.4 and 582.8 μmol·h⁻¹·g_cat⁻¹. Conversely, in water/triethanolamine systems, methanol production reached 3061.6 μmol·h⁻¹·g_cat⁻¹, with 94.79% of the initial conversion retained after three cycles. Finally, this work ends with the conclusions of the CO₂ photocatalytic reduction to formic acid, acetic acid, and methanol, and recommends prospects for future research. Full article

Titanium dioxide (TiO₂), a widely used semiconductor in photocatalysis owing to its adequate potential for water hydrolysis, chemical stability, low toxicity, and low cost. However, its efficiency is limited by fast charge-carrier recombination and poor visible light absorption. Coupling TiO₂ with a p-type semiconductor, such as nickel oxide (NiO), forming a p-n heterojunction, decreases the recombination of charge carriers and increases photocatalytic activity. In this work, the surface of TiO₂ modified with NiO nanoparticles (NPs) induced by radiolysis for photocatalytic hydrogen production was studied. The photocatalytic activity of NiO/TiO₂ was evaluated using methanol as a hole scavenger under UV–visible light. All modified samples presented superior photocatalytic activity compared to bare TiO₂. The dynamics of the charge carriers, a key electronic phenomenon in photocatalysis, was investigated by time-resolved microwave conductivity (TRMC). The results highlight the crucial role of Ni-based NPs modification in enhancing the separation of the charge carrier and activity under UV–visible irradiation. Furthermore, the results revealed that under visible irradiation, NiO-NPs inject electrons into the conduction band of titanium dioxide. Full article

This study investigates the catalytic potential of silver nanoparticles (AgNPs) synthesized using aqueous Cymbopogon citratus (lemongrass) extract for the degradation of toxic textile dyes, offering an eco-friendly solution to industrial wastewater treatment. The green-synthesized AgNPs demonstrated remarkable degradation efficiency (>94%) for multiple dyes, such as rhodamine B, methyl red, methyl orange, methylene blue, eosin yellow, and Eriochrome black T, in the presence of sodium borohydride. Optimization studies employing a one-factor-at-a-time approach revealed the critical influence of AgNPs and reductant concentration, temperature, and pH. Kinetic analysis confirmed pseudo-first-order degradation behavior. Reactive species scavenging experiments established that hydroxyl radicals and holes played dominant roles in the degradation mechanism. Notably, the AgNPs retained catalytic activity across eight reuse cycles with negligible performance loss, demonstrating strong potential for repeated application. Comparative analysis with data from the literature highlights the superior performance of C. citratus-derived AgNPs in terms of reaction rate and efficiency. This work underscores the value of plant-extract-mediated AgNPs synthesis not only for its environmental compatibility but also for its catalytic effectiveness. The study advances the practical applicability of green nanotechnology in wastewater remediation and supports its integration into sustainable industrial practices. Full article

Tetracycline hydrochloride pollution poses a serious environmental threat; however, it is difficult to deal with by conventional methods. In this study, the Z-scheme BiOCl/Bi₂WO₆ composite was hydrothermally synthesized and evaluated for its ability to decompose tetracycline hydrochloride under visible light. The composite material was systematically characterized by XRD, SEM, TEM/HRTEM, XPS, FTIR, BET, PL, UV-Vis DRS, and EPR to analyze its structure, morphology, and optical/electrochemical properties. Characterization revealed that the composite featured a flower-ball structure with broader light absorption and higher solar energy efficiency. A narrow bandgap further facilitated charge separation, boosting photocatalytic performance. Among the synthesized materials, the 20% BiOCl/Bi₂WO₆ composite exhibited the best performance, removing 94% of tetracycline hydrochloride in 60 min, which was 5.2 times and 1.4 times higher than pure BiOCl and Bi₂WO₆, respectively. The rate constant was 10.8 times and 2.5 times higher than that of pure BiOCl and Bi₂WO₆. After five cycles, it maintained the 88.7% removal rate, with X-ray diffraction analysis confirming its structural stability and well mechanical properties. Electron paramagnetic resonance and radical scavenging experiments identified photogenerated holes (h⁺) and superoxide radicals (·O₂⁻) as the primary active species. This work highlights the fact that the prepared Z-scheme BiOCl/Bi₂WO₆ composite exhibited excellent photocatalytic performance in the degradation of tetracycline hydrochloride, demonstrating promising potential for practical applications. Full article

Graphene quantum dots (GQDs) show significant promise as antibacterial agents, but their application is hindered by several limitations, including potential cytotoxicity at high concentrations, as well as concerns regarding aggregation and reusability. In this study, sodium titanate (NTO) ultralong nanotubes were utilized as both a photocatalyst and support for GQDs. The NTO/GQDs heterojunction was formed by embedding GQDs nanoplates onto the walls of NTO nanotubes. This integration significantly improved the visible light absorption and enhanced the separation and transfer of electron–hole pairs, leading to an efficient photocatalytic antibacterial process. The NTO/GQD-8 self-supporting membrane composed of these ultralong nanotubes demonstrated outstanding antibacterial efficiency (99.99%) against E. coli and exhibited remarkable cycling stability. Radical scavenging experiments revealed that ∙OH and e⁻ were the primary reactive species driving the photocatalytic antibacterial process. Notably, NTO and NTO/GQDs-8 exhibited distinct antibacterial outcomes. After photocatalytic treatment with NTO/GQDs-8, E. coli cells were completely fragmented, with no intact cell structures remaining due to the synergy effect of GQDs’ physical cutting during photocatalytic treatment. Full article

Cu₂O, a narrow-bandgap semiconductor with visible light absorption capabilities, faces limitations in photocatalytic applications due to photocorrosion from hole self-oxidation and insufficient light absorption. In this work, a series of novel spherical Cu₂O/FePO₄ Z-scheme heterojunctions were successfully synthesized via self-assembly to overcome these challenges. The photocurrent, electrical impedance spectroscopy (EIS), and photoluminescence (PL) tests showed that Cu₂O/1.5FePO₄ (CF1.5) had excellent electron hole separation efficiency. Subsequently, photocatalytic degradation was utilized as a probing technique to further confirm the above conclusions, with the kinetic reaction constants of CF1.5 being 2.46 and 11.23 times higher than those of Cu₂O and FePO₄, respectively. After five cycles of experiments and XPS analysis, it was found that the content of Cu(I) in CF1.5 did not significantly decrease after the reaction, indicating that it has superior anti-photocorrosion performance compared to single Cu₂O, which is also due to the establishment of a Z-scheme heterojunction. Systematic studies using radical scavenging experiments and ESR tests identified ·OH and ·O₂⁻ as the main active species involved in photocatalysis. The formation of a Z-scheme heterojunction not only enhances the photocatalytic activity of the CF1.5 composite but also effectively suppresses the photocorrosion of Cu₂O, thereby offering a promising approach for enhancing anti-photocorrosion of Cu₂O. Full article

Furazolidone, a nitrofuran antibiotic, has been broadly used in aquaculture and veterinary medicine, and its presence in water poses considerable environmental and health hazards due to its toxicity. This study investigated a hybrid photocatalytic process for the removal of furazolidone, employing graphitic carbon nitride (g-C₃N₄) and persulfate anions (PS) under both laboratory and pilot-scale conditions. The synergistic effect of g-C₃N₄ and PS enhanced the generation of reactive species, facilitating the efficient degradation of FZ in two different aqueous matrices. Through scavenging studies, positive holes were determined to be the dominant reactive species, followed by sulfate radicals. Seven transformation products of FZ were tentatively identified via UHPLC-LTQ/Orbitrap MS analysis. The optimized photocatalytic system (g-C₃N₄/PS) achieved a 100% removal of furazolidone in less than 60 min under simulated solar light, demonstrating its potential for large-scale application in wastewater remediation. Furthermore, pilot-scale experiments using real secondary treated municipal wastewater proved that the applied process is capable of achieving an 86.2% removal of furazolidone (k = 0.017 min⁻¹) as well as a 90% decrease in effluent ecotoxicity within 120 min of UV_A irradiation. This study provides insights into sustainable processes for the removal of antibiotic contaminants from wastewater and underscores the role of g-C₃N₄-based photocatalytic approaches in upper-scale applications. Full article

This work examines the solar photocatalytic degradation of the antibiotic sulfamethoxazole (SMX) using molybdenum telluride (MoTe₂)-promoted bismuth oxychloride (BiOCl). Different loadings of molybdenum telluride in the 0–1% range on BiOCl were synthesized and evaluated. Although the presence of MoTe₂ did not alter either the adsorption capacity or the energy gap of BiOCl, the synthesized photocatalyst demonstrated higher photocatalytic activity due to the enhanced separation of photogenerated pairs. The 0.5MoTe₂/BiOCl photocatalyst achieved a kinetic constant nearly 2.8 times higher than that of pure BiOCl, leading to the elimination of 500 μg/L SMX within 90 min. The system’s performance was enhanced under neutral to acidic conditions and lower SMX concentrations. Based on experiments with radical scavengers, photogenerated holes appeared to be the dominant species, with the contribution of reactive species following the order ${\mathrm{h}}^{+}>{\mathrm{O}}_2^{•-}/{\mathrm{e}}^{-}>$¹${\mathrm{O}}_2{>\mathrm{H}\mathrm{O}}^{•}$. Interestingly, in different water matrices, photocatalytic activity was not diminished and even increased by 20%, likely because of the action of photogenerated holes and the selectivity of secondary generated radicals. The photocatalyst retained > 90% of its activity after three sequential experiments. Finally, four transformation products from SMX photodegradation were identified via UHPLC-TOF-MS, and a degradation pathway is proposed. Full article

The textile industry is a major contributor to environmental pollution, primarily through the discharge of wastewater loaded with dyes and contaminants that disrupt natural ecosystems. This study aims to develop a hybrid material by functionalizing carbon nanodots (CNDs) with the donor-π-acceptor organic dye L1 via amide coupling. By chemically modifying the surface of CNDs, we can enhance their multifunctionality and tailor their molecular composition. This innovative approach seeks to replace expensive dyes with cost-effective CNDs synthesized from citric acid and ethylenediamine using a domestic microwave oven, potentially improving the stability of the resulting hybrid. Additionally, TiO₂ anatase particles were synthesized as a metal oxide platform and sensitized with both pristine materials and the CND-L1 hybrid. A range of physicochemical methods was employed to analyze the elemental, structural, and optical properties of these materials. In photocatalytic degradation tests of methyl orange, the sensitized catalysts demonstrated significantly improved efficiency compared to TiO₂ alone. While CNDs exhibited good stability and enhanced L1’s stability, scavenger experiments revealed that holes and hydroxyl radicals play crucial roles in the degradation mechanism. This research underscores the promise of CND hybrids in advancing pollutant degradation technologies while reducing reliance on costly photocatalysts. Full article

Photocatalytic technology holds significant promise for sustainable development and environmental protection due to its ability to utilize renewable energy sources and degrade pollutants efficiently. In this study, BiOI nanosheets (NSs) were synthesized using a simple water bath method with varying amounts of mannitol and reaction temperatures to investigate their structural, morphological, photoelectronic, and photocatalytic properties. Notably, the introduction of mannitol played a critical role in inducing a transition in BiOI from an n-type to a p-type semiconductor, as evidenced by Mott–Schottky (M-S) and band structure analyses. This transformation enhanced the density of holes (h⁺) as primary charge carriers and resulted in the most negative conduction band (CB) position (−0.822 V vs. NHE), which facilitated the generation of superoxide radicals (·O²⁻) and enhanced photocatalytic activity. Among the samples, the BiOI-0.25-60 NSs (synthesized with 0.25 g of mannitol at 60 °C) exhibited the highest performance, characterized by the largest specific surface area (24.46 m²/g), optimal band gap energy (2.28 eV), and efficient photogenerated charge separation. Photocatalytic experiments demonstrated that BiOI-0.25-60 NSs achieved superior methylene blue (MB) degradation efficiency of 96.5% under simulated sunlight, 1.14 times higher than BiOI-0-70 NSs. Additionally, BiOI-0.25-60 NSs effectively degraded tetracycline (TC), 2,4-dichlorophenol (2,4-D), and rhodamine B (Rh B). Key factors such as photocatalyst concentration, MB concentration, and solution pH were analyzed, and the BiOI-0.25-60 NSs demonstrated excellent recyclability, retaining over 94.3% of their activity after three cycles. Scavenger tests further identified ·O²⁻ and h⁺ as the dominant active species driving the photocatalytic process. In this study, the pivotal role of mannitol in modulating the semiconductor characteristics of BiOI nanomaterials is underscored, particularly in promoting the n-type to p-type transition and enhancing photocatalytic efficiency. These findings provide a valuable strategy for designing high-performance p-type photocatalysts for environmental remediation applications. Full article

Piezocatalytic materials have attracted widespread attention in the fields of clean energy and water treatment because of their ability to convert mechanical energy directly into chemical energy. In this study, γ-AlON particles synthesised using carbothermal reduction and nitridation (CRN) were used for the first time as a novel piezocatalytic material to degrade dye solutions under ultrasonic vibration. The γ-AlON particles exhibited good performance as a piezocatalytic material for the degradation of organic pollutants. After 120 min under ultrasonic vibration, 40 mg portions of γ-AlON particles in 50 mL dye solutions (10 mg/L) achieved 78.06%, 67.74%, 74.29% and 64.62% decomposition rates for rhodamine B (RhB), methyl orange (MO), methylene blue (MB) and crystal violet (CV) solutions, respectively; the fitted k values were 13.35 × 10⁻³, 10.79 × 10⁻³, 12.09 × 10⁻³ and 8.00 × 10⁻³ min⁻¹, respectively. The piezocatalytic mechanism of γ-AlON particles in the selective degradation of MO was further analysed in free-radical scavenging activity experiments. Hydroxyl radicals (•OH), superoxide radicals (•O₂⁻), holes (h⁺) and electrons (e⁻) were found to be the main active substances in the degradation process. Therefore, γ-AlON particles are an efficient and promising piezocatalytic material for the treatment of dye pollutants. Full article

With the intensification of the energy crisis and the growing concern over environmental pollution, particularly the discharge of organic dye pollutants in industrial wastewater, photocatalytic degradation of these contaminants using solar energy has emerged as an effective, eco-friendly solution. In this study, we successfully synthesized 2D/2D g-C₃N₄/BiOI p-n heterojunctions via a simple precipitation method and a high-temperature calcination method. The unique 2D structures of g-C₃N₄ nanosheets (NSs) and BiOI NSs, coupled with the synergistic effect between the two materials, significantly enhanced the photocatalytic degradation performance of the heterojunctions under simulated sunlight. The band structures, as determined by Tauc curves, Mott–Schottky curves and XPS-VB analysis, revealed a Z-scheme charge transfer mechanism that efficiently reduced charge carrier recombination and improved electron–hole separation. The photocatalytic activity of 2D/2D g-C₃N₄/BiOI p-n heterojunctions for rhodamine B (Rh B) degradation reached 99.7% efficiency within 60 min, a 2.37-fold and 1.27-fold improvement over pristine BiOI NSs and g-C₃N₄ NSs, respectively. Furthermore, the heterojunction exhibited excellent recyclability stability, with the degradation efficiency decreasing by only 1.2% after five cycles. Radical scavenging experiments confirmed the involvement of superoxide radicals (∙O₂⁻) and hydroxyl radicals (∙OH) as the primary reactive species in the degradation process. This work highlights the potential of 2D/2D g-C₃N₄/BiOI p-n heterojunctions for efficient photocatalytic applications in environmental remediation. Full article

Anodic TiO₂ nanotube arrays decorated with Ni, Cu, and NiCu alloy thin films were investigated for the first time for the photocatalytic degradation of paracetamol in water solution under UV irradiation. Metallic co-catalysts were deposited on TiO₂ nanotubes using magnetron sputtering. The influence of the metal layer composition and thickness on the photocatalytic activity was systematically studied. Photocatalytic experiments showed that only Cu-rich co-catalysts provide enhanced paracetamol degradation rates, whereas Ni-modified photocatalysts exhibit no improvement compared with unmodified TiO₂. The best-performing material was obtained by sputtering a 20 nm thick film of 1:1 atomic ratio NiCu alloy: this material exhibits a reaction rate more than doubled compared with pristine TiO₂, enabling the complete degradation of 10 mg L⁻¹ of paracetamol in 8 h. The superior performance of NiCu-modified systems over pure Cu-based ones is ascribed to a Ni and Cu synergistic effect. Kinetic tests using selective holes and radical scavengers unveiled, unlike prior findings in the literature, that paracetamol undergoes direct oxidation at the photocatalyst surface via valence band holes. Finally, Chemical Oxygen Demand (COD) tests and High-Resolution Mass Spectrometry (HR-MS) analysis were conducted to assess the degree of mineralization and identify intermediates. In contrast with the existing literature, we demonstrated that the mechanistic pathway involves direct oxidation by valence band holes. Full article