Search Results (1,309)

An optimum In_0.2Cd_0.8S composition was synthesized with graphene to enhance photocatalytic performance. Graphene incorporation altered the morphology from compact grains to a loosely aggregated structure without affecting the crystal phase, as confirmed by XRD. XPS analysis indicated surface-level interaction between graphene and the In–Cd–S matrix, rather than lattice integration. Mott–Schottky and Kubelka–Munk analyses revealed n-type semiconducting behavior and a slight band gap increase from 2.46 to 2.51 eV upon graphene blending. UV–Vis and IPCE measurements showed enhanced light absorption, with IPCE values of 9.33% and 5.01% at 380 nm and 480 nm, respectively. The 3.85 wt% graphene-modified photocatalyst achieved a hydrogen evolution rate of 4.97 μmolh⁻¹cm⁻², more than triple that of pristine In_0.2Cd_0.8S. These enhancements are attributed to improved charge transport and interfacial activity provided by the graphene. Full article

With the rapid development of the edible fungus industry, the environmental pressure and resource waste caused by the massive generation of fungal residue have become increasingly prominent. Meanwhile, heavy metal wastewater pollution and the growing demand for clean energy pose dual challenges to sustainable development. This study focuses on Auricularia cornea var. Li. fungal residue, exploring the establishment of a multi-level resource utilization pathway integrating “porous carbon material preparation—heavy metal adsorption—photocatalytic hydrogen evolution.” Firstly, the Auricularia cornea var. Li. residue-based porous carbon material was examined by combining hydrothermal carbonization, activation and slow pyrolysis. In optimal conditions, the porous carbon obtained yielded a surface area of 675.56 m²/g and formed a composite pore structure consisting of micropores with coexisting micropore and mesopore. Secondly, we performed batch adsorption experiments to study the effects of solution pH, adsorbent dosage and contact time and the adsorption behavior via fitting adsorbing kinetic models. Under optimal conditions, Cd(II) removal efficiency reached 92.36% and an equilibrium adsorption capacity of 92.47 mg/g. We used Cd(II) adsorbed porous carbon as a cadmium source and converted into a CdS photocatalyst using a hydrothermal sulfidation process. The CdS prepared using sodium sulfide as a sulfur source gave an average hydrogen evolution rate of 668.01 μmol·g⁻¹·h⁻¹ and showed higher photocatalytic performance for water splitting to produce hydrogen. Full article

Polycyclic aromatic hydrocarbons (PAHs) are highly toxic pollutants in marine ecosystems, necessitating efficient remediation. This study synthesized magnesium phthalocyanine (MgPc) and its modified derivatives, magnesium azaphthalocyanine (NMgPc) and methyl-substituted magnesium azaphthalocyanine (MeNMgPc), as visible-light-driven photocatalysts for PAH degradation. To enhance efficiency and recoverability, these photosensitizers were immobilized onto coconut shell activated carbon (AC) via multiple ultrasonic impregnation. Characterizations (UV-Vis, SEM, EDAX, BET) confirmed successful active component deposition; nitrogen substitution and peripheral methyl groups synergistically tuned the electronic structure and suppressed aggregation. Under xenon lamp irradiation, the MeNMgPc/C composite exhibited superior activity, degrading 90.55% of naphthalene. Box-Behnken response surface optimization identified optimal conditions (13.18 g/L dosage, 20 A, 2.28 h), yielding 96.67% experimental removal and adhering to pseudo-first-order kinetics. Mechanistic studies via electron spin resonance identified hydroxyl (•OH) and superoxide radicals (O₂^•−) as primary reactive species. GC-MS analysis elucidated a sequential phenanthrene ring-opening pathway, progressing to ultimate mineralization into CO₂. Consequently, MeNMgPc/C presents a highly efficient, recoverable photocatalytic platform for marine PAH remediation. Full article

Ternary heterojunction photocatalysts enhance the separation and transport of photogenerated charge carriers, thereby boosting their redox activity for use in environmental and sustainable energy applications. This study focuses on the synthesis of a TiO₂/Bi₂O₃/g-C₃N₄ heterojunction composite via a ceramic method with TiO₂ loadings of 80%, 85%, and 90% (denoted 80T-BC, 85T-BC, and 90T-BC, respectively) to investigate structure–property–performance relationships in photocatalytic dye degradation. The structural, optical, and morphological properties of the synthesised materials were characterised using X-ray diffraction (XRD), scanning electron microscopy (SEM), and diffuse reflectance UV–Vis spectroscopy (DRS). The photocatalytic performance was evaluated by measuring the degradation of Rhodamine B under visible light irradiation. Under optimised conditions (pH 6, initial RhB concentration of 5 mg/L, and a reaction time of 120 min), a degradation rate of 99% was achieved. Furthermore, the semiconductor demonstrated significant antibacterial activity against both Gram-negative (Pseudomonas aeruginosa) and Gram-positive (Staphylococcus aureus) bacteria. This study presents a promising strategy for modifying TiO₂-based semiconductors by incorporating different metal oxides. The formation of the resulting heterojunction significantly enhances photocatalytic efficiency, demonstrating strong potential for practical environmental remediation. Full article

This study presents the rational design of a visible-light-responsive TiO₂/polyaniline (PANI) nanofiber heterostructure via in situ oxidative polymerization to overcome the limited visible-light absorption and rapid charge recombination of TiO₂. Comprehensive characterization using XRD, FT-IR, XPS, SEM, UV–Vis DRS, and EIS confirmed the successful integration of TiO₂ nanoparticles within a conductive polyaniline nanofiber network, enabling efficient interfacial charge transfer. The optimized TiO₂/PANI-30 composite exhibited outstanding photocatalytic performance, achieving ~99% degradation of Basic Fuchsin dye within 40 min under visible light, significantly outperforming pristine TiO₂. The enhanced activity is attributed to improved visible-light absorption, reduced bandgap energy, and suppressed electron–hole recombination, supported by optical and electrochemical analyses. Kinetic studies indicated pseudo-first-order behavior, with TiO₂/PANI-30 showing the highest rate constant. Radical trapping experiments identified superoxide and hydroxyl radicals as the main active species, with •OH playing a dominant role. A direct Z-scheme charge transfer mechanism was suggested, preserving strong redox potentials and promoting reactive oxygen species generation. Additionally, the photocatalyst demonstrated excellent stability and reusability. These findings highlight the suggested potential of TiO₂/PANI systems as efficient and sustainable photocatalysts for wastewater treatment. Full article

In the current research, graphene and cellulose nanocrystals (CNCs) loaded with silver nanoparticles were synthesized using the hydrothermal method with different mass ratios (G:CNC:CS). The composite GC2 (1:0.2:0.2) (MIC = 6.1 µg·mL⁻¹) and GC3 (1:0.3:0.3) (MIC = 1.8 µg·mL⁻¹) exhibited the maximum antibacterial activity against Staphylococcus aureus subsp. aureus ATCC BAA-977 and Pseudomonas aeruginosa, respectively. The antibacterial performance underscores the complex interplay between the compositional attributes of GC2 and GC3, and the unique susceptibility profiles of different bacterial strains. The antibacterial mechanism was proposed to understand the antibacterial activity process. Ag⁺ cations and reactive oxygen species (ROS) formed with the composite materials are responsible for disrupting interactions with the bacterial cell wall via transmembrane proteins. Eriochrome Black T exhibited the highest photocatalytic degradation efficiency (~90% under UV), followed by Congo Red, which also showed substantial removal across all irradiation conditions. In contrast, Bisphenol A and tetracycline displayed comparatively lower degradation efficiencies, particularly under UV light. Overall, the degradation trend for all pollutants followed the order: UV > solar > visible irradiation. Full article

The efficient photocatalytic generation of hydrogen peroxide (H₂O₂) from pure water remains a formidable challenge, primarily due to the rapid recombination of photogenerated electron–hole pairs and insufficient redox potentials inherent in single-component photocatalysts. To address these issues, we designed and synthesized a heterojunction material comprising cadmium sulfide nanoparticles loaded on carbon spheres (CS@CdS). Under conditions utilizing pure water and ambient air, the CS@CdS composite achieves an H₂O₂ production rate of 1305 μmol·g⁻¹·h⁻¹, which is 3.1 and 3.6 times higher than that of pure CdS and CS, respectively, without the need for any sacrificial agents or external oxygen supply. Systematic characterization reveals that CS and CdS form a tightly coupled electronic interface, which significantly accelerates charge carrier separation and effectively prolongs the lifetime of photogenerated carriers, thereby boosting photocatalytic performance. Furthermore, the CS component extends the visible-light absorption range of the composite and functions as an electron acceptor to suppress charge recombination, collectively endowing CS@CdS with enhanced photocatalytic activity. Mechanistic studies indicate that H₂O₂ production over CS@CdS proceeds predominantly via a two-step single-electron oxygen reduction reaction (ORR) pathway. This work offers a viable strategy for constructing CS-based heterojunction photocatalysts for efficient H₂O₂ synthesis. Full article

Textile wastewater is among the most challenging industrial effluents due to its complex composition, high pollutant load, and low biodegradability. Conventional treatment methods often fall short in achieving complete removal of dyes and emerging contaminants. Photocatalytic composite membranes have emerged as a promising solution by integrating membrane separation and advanced oxidation processes. This review provides a comprehensive overview of the design, fabrication, and performance of photocatalytic composite membranes for textile wastewater treatment. Key aspects include the types of photocatalysts employed, methods of incorporation into membranes, and their synergistic role in pollutant removal and membrane fouling mitigation. Recent advancements in materials science, such as visible-light-responsive catalysts, carbon-based nanocomposites, and self-cleaning surfaces, are discussed, along with current limitations related to catalyst stability, operational scalability, and cost. This review underscores the potential of photocatalytic composite membranes as a next-generation platform for sustainable and effective textile wastewater treatment. Full article

The photocatalytic activity of TiO₂ can be increased by incorporating it into a composite with an electron-trapping co-catalyst. MXene can perform this task as an electron-conducting material. In addition to trapping electrons, it also affects the defects in TiO₂ near the interface. To screen for the best photocatalytic performance, three types of composites were prepared: by physical mixing, chemical deposition, and ALD. During characterization, the structural, optical, and photoelectrochemical properties were determined. Photocatalytic activity was examined in suspension (phenol conversion) and on a layer (gas phase ethanol conversion). It was found that the composite containing the lowest proportion of cocatalyst (1 wt.%) had the highest photocatalytic activity. According to the results of photocatalytic activity measured in suspension, the physical mixtures were proven to be more effective than neat TiO₂, with the composites converting approximately the total amount of phenol in ~40 min, while TiO₂ required ~80–90 min to do so under the same conditions. Thus, the electron-trapping role of MXene is clearly demonstrated in suspension applications, which is also confirmed by other characterization methods (photoluminescence, photocurrent density). TiO₂ performed best during ethanol conversion, as it has the highest ethanol adsorption capacity (33.41%). During ethanol conversion tests, the MXene electron-trapping property was most effectively demonstrated in composites formed using the ALD method. Full article

To improve the visible-light-driven photocatalytic degradation efficiency of g-C₃N₄-based photocatalysts toward organic pollutants, a MoS₂/g-C₃N₄ composite precursor was employed in this work, and the phase composition and defect environment of Mo species were regulated by post-annealing under air and N₂ atmospheres, respectively, thereby constructing Mo-based/g-C₃N₄ (MCN) composites with distinct structural evolution characteristics. The results showed that the photocatalytic activity of the as-sonicated MCN composite toward methylene blue (MB) was only moderately improved, among which the 15% loading sample exhibited the best performance with a degradation efficiency of about 42.0% within 60 min. In contrast, annealing at 400 °C under N₂ resulted in only a slight activity change, whereas the sample treated at 400 °C in air (Air-15% MCN) achieved an MB degradation efficiency of 99.9% within 60 min, together with a much higher pseudo-first-order reaction rate constant than that of the air-treated sample at a lower temperature. XRD, FT-IR and XPS analyses revealed that air annealing induced the conversion of MoS₂ into highly crystalline MoO₃ (or MoO_3−x), leading to the formation of a reconstructed MoO_3−x/g-C₃N₄ composite interface. Meanwhile, the increased high-binding-energy component in the O 1s spectrum and the EPR signal around g ≈ 2.00 further suggested the presence of more abundant defect-related centers in the air-treated sample. Although Air-15% MCN possessed a lower specific surface area than the untreated and N₂-treated samples, it displayed enhanced visible-light absorption, higher transient photocurrent response, lower interfacial charge-transfer resistance, and accelerated carrier dynamics, indicating that the activity enhancement mainly originated from atmosphere-induced phase transformation, interfacial reconstruction, defect-related active centers, and improved charge separation/transfer, rather than from the surface area effect. Based on the above results, a possible interfacial charge-transfer pathway is tentatively proposed for the g-C₃N₄/MoO_3−x interface formed after air treatment, which contributes to the efficient utilization of photogenerated carriers and the rapid degradation of MB. This work demonstrates that atmosphere-induced phase transformation is a simple and effective strategy for regulating the structure and photocatalytic performance of Mo-based/g-C₃N₄ composites, and provides useful guidance for the design of efficient visible-light photocatalysts. Full article

Industrial dye wastewater poses serious environmental and health risks, demanding sustainable remediation strategies. Here, hierarchically porous hollow TiO₂ nanofibers (HNFTis) were fabricated and combined with blue, green, and orange graphene quantum dots (b-GQDs, g-GQDs, o-GQDs) to form heterojunction photocatalysts. Progressive fluorescence redshift of GQDs, induced by surface functionalization and S/B doping, narrows the bandgap and enhances visible-light absorption. Among the composites, 0.5 wt% o-GQDs/HNFTi exhibited the highest photocurrent and lowest charge-transfer resistance and degraded 99.5% of Methylene blue under visible light within 2 h, outperforming pristine HNFTi (77.7%). The synergistic effect of TiO₂ structural engineering and GQD fluorescence tuning demonstrates an effective strategy for designing high-performance photocatalysts for sustainable wastewater treatment. Full article

An effective strategy for significantly enhancing photocatalytic activity of composite materials is to construct heterojunctions. Herein, a series of imidazole-modified heterostructured g-C₃N₄/SnO (CNIS) Z-scheme photocatalysts were prepared by calcination methods, leading to superior photocatalytic performance than pure SnO and imidazole-modified g-C₃N₄. Rhodamine B (Rh B) aqueous solution was taken as the target pollutant, and the result presented that both imidazole modification and the Z-scheme heterojunction construction benefited from significant enhancement in photocatalytic activity. Moreover, it is revealed that electrons were transferred from imidazole-modified g-C₃N₄ to SnO through the interface of the composite by XPS analysis. Under visible light (>420 nm) irradiation, the built-in electric field, band edge bending, and Coulomb interaction work synergistically to drive the recombination of relatively useless electrons and holes in the hybrid. As a result, the residual electrons and holes, which possess enhanced reducibility and oxidizability, endow the composite with exceptional redox capability. This research can not only deepen our comprehension of designing and fabricating innovative Z-scheme heterojunction photocatalysts but also presents an effective approach to tackle environmental pollution issues in the future. Full article

Imidazolinone herbicides such as imazethapyr (IMT) pose potential ecological risks due to their high mobility and ecotoxicity. This study synthesized the bismuth-based photocatalyst BiOIO₃ via a facile hydrothermal method and systematically characterized its physicochemical properties. BiOIO₃ features a 2D lamellar structure, pure phase composition, and a built-in internal polarization electric field that efficiently separates photogenerated electron–hole pairs. Photocatalytic experiments exhibited that BiOIO₃ achieved 84.5% elimination of IMT, with a rate constant 66 times higher than that of TiO₂ (Rutile). Mechanistic studies revealed that photogenerated electrons (e⁻), holes (h⁺), and superoxide radicals (·O₂⁻) are the primary reactive species. HPLC-MS/MS identified key intermediates, and QSAR-based toxicity prediction showed reduced mutagenicity for most intermediates. Importantly, BiOIO₃ effectively eliminated five imidazolinone herbicides simultaneously. This work highlights BiOIO₃ as a promising photocatalyst for efficient and practical remediation of imidazolinone herbicide-contaminated water. Full article

In this study, a cellulose nanocrystal (CNC)-supported Ag–ZnO nanocomposite was synthesized via a hydrothermal route as a polymeric photocatalyst for efficient UV-A light-driven dye degradation. The renewable CNC framework provides abundant hydroxyl functional groups for nanoparticle anchoring, enhancing dispersion and interfacial charge transfer. Structural (XRD, FTIR, TEM, PL, and XPS) and thermal (TGA and DTG) analyses confirm successful incorporation of Ag nanoparticles and retention of CNC crystallinity. The composite exhibits a reduced optical bandgap (3.02 eV) and demonstrates superior photocatalytic activity, achieving 96% methylene blue (MB) degradation within 120 min. Enhanced performance is attributed to the synergistic effect of Ag-induced plasmonic excitation and CNC-facilitated charge migration, effectively suppressing ZnO photocorrosion. Moreover, the optimization of the parameters was conducted and found to be pH 7, a catalyst dose of 0.3 g L⁻¹, and an initial MB concentration of 10 ppm, which shows the best photocatalytic degradation reaction. The CNC/Ag–ZnO catalyst maintains 87% activity after five reuse cycles, showing good stability and reusability. The photostability of the CNC/Ag–ZnO catalyst was evaluated by ICP-MS, which measured Zn²⁺ concentration in the aqueous solution. Additionally, the degraded MB compounds were identified using GC-MS/MS analysis. This work highlights the potential of polymer-based biogenic supports for sustainable photocatalyst design and bridges polymer science with environmental remediation technology. Full article

Hydrogen peroxide (H₂O₂) is an important green oxidant, and developing efficient visible-light-driven routes for its synthesis is highly desirable. Herein, a CN/Zn_V-ZCS composite photocatalyst was constructed by coupling g-C₃N₄ (CN) with Zn-vacancy-containing ZnCdS (Zn_V-ZCS) for photocatalytic H₂O₂ production. The optimized CN/Zn_V-10 delivered 44.58 mmol g⁻¹ H₂O₂ within 60 min under 425 nm LED irradiation, outperforming pristine CN, ZCS, Zn_V-ZCS, and vacancy-free CN/ZCS, with good cycling stability. Trapping and EPR results identify O₂ as the key electron acceptor and ·O₂⁻ as an important intermediate. Structural characterization and XPS results indicate successful Zn-vacancy introduction, intimate heterointerface formation, and interfacial electron redistribution. Combined VB-XPS, photoelectrochemical, and reactive-species analyses suggest that Zn vacancies are favorable for O₂ adsorption/activation, whereas the CN/Zn_V-ZCS heterointerface promotes charge separation and migration. Based on the available evidence, a Z-scheme interfacial charge-transfer pathway is established in the CN/Zn_V-ZCS system. Full article