Search Results (136)

In this work, different materials based on TiO₂ coupled with either AgBr or Ag₃PO₄ were synthesized. The Ag₃PO₄(50%)/TiO₂ powder photocatalyst prepared by deposition–precipitation method showed higher antimicrobial activity than the bare TiO₂ and also than the same coupled powder obtained by sol–gel method. This material achieved 100% E. coli, coliforms, and other enterobacteria elimination. The high bactericidal efficiency of this material could be attributed to the improved properties obtained by coupling Ag₃PO₄ and TiO₂, such as high absorption in the visible region, low band-gap value, and high surface hydroxylation. The sol–gel method was chosen for the production of photocatalytic coatings on borosilicate glass tubes based on TiO₂ and Ag₃PO₄/TiO₂ materials due to the ease of its preparation procedure and its suitability for dip coating. In this series, the most effective elimination of E. coli, coliforms, and other enterobacteria was achieved with the glass tubes coated with the laboratory–prepared TiO₂ sol. Interestingly, this material presented superior antimicrobial performance as coating (100% of E. coli elimination) compared to its powder form. The titania coating also showed the best efficiency in the degradation of methylene blue (i.e., 95.2%), though this material lost 30% of its photoactivity after four reaction cycles. Full article

Finding high-performance and low-cost materials is essential for high-quality photocatalytic water purification to expand the spectral response and improve light utilization. In this paper, we used relatively inexpensive materials such as Ag and TiO₂. The influence of particle spacing, core radius, shell thickness, environmental refractive index, and incident light direction angle on the light absorption and scattering properties, local electric field enhancement, and photothermal effect of the Ag@TiO₂ core–shell nanosphere dimer is investigated by using the finite element method and the finite difference time domain. The formation mechanism of multipole resonance mode of the dimer is revealed by means of the multipole decomposition theory and the internal current distribution of the particles. The results show that light absorption and scattering of the dimer can be tuned within the visible light range by changing the particle spacing, core radius, and shell thickness. With the azimuth angle of incident light increases, the longitudinal local surface plasmon resonance (L-LSPR) mode will transform into the transverse local surface plasmon resonance (T-LSPR) mode, and the L-LSPR mode makes the dimer have better local electric field enhancement. Strong light absorption can easily cause a sharp increase in the temperature around the dimer, accelerating the rate of catalytic oxidation reactions and the elimination of bacteria and viruses in water. Strong light scattering causes a significant enhancement of the electric field between the particles, making the generation of hydroxyl and other active oxides more efficient and convenient. This work establishes a theoretical basis for designing efficient water purification photocatalysts. Full article

Dye-contaminated wastewater has become one of the most severe environmental challenges due to the non-biodegradability and toxicity of synthetic dyes. While photocatalytic degradation is considered a green and efficient technology for wastewater purification, conventional TiO₂ suffers from limited light utilization and rapid electron–hole recombination. In this exploration, Ag-TiO₂-RGO nanocomposites were successfully fabricated and systematically investigated by XRD, SEM, TEM, XPS, Raman, and PL spectroscopy. The incorporation of Ag nanoparticles and reduced graphene oxide (RGO) synergistically improved charge separation and transfer efficiency. Photocatalytic activity was evaluated using different dyes as pollutants under visible light irradiation. Among the samples, Ag-TiO₂-RGO-3% exhibited the highest RhB degradation efficiency of 99.5% within 75 min, with a rate constant (K) of 0.05420 min⁻¹, which was nearly three times higher than that of pure TiO₂. The photocatalyst also showed excellent reusability with only minor efficiency loss after five cycles, and its activity remained stable across a wide pH range. Radical trapping experiments revealed that •O₂⁻ served as the dominant reactive species, with additional contributions from •OH and photogenerated holes (h⁺). A possible photocatalytic mechanism was proposed, in which Ag nanoparticles and RGO effectively suppressed electron–hole recombination and accelerated the formation of reactive oxygen species for efficient dye mineralization. These findings demonstrate that Ag-TiO₂-RGO-3% is a promising photocatalyst with high activity, stability, and environmental adaptability for wastewater remediation. Full article

The persistent release of synthetic dyes such as methylene blue (MB) into aquatic environments poses a significant ecological hazard due to their chemical stability and toxicity. In recent years, the application of engineered composite photocatalysts has emerged as a potent solution for efficient dye degradation under visible and UV light. This review comprehensively summarizes various advanced composites, including carbon-based, metal-doped, and heterojunction materials, tailored for MB degradation. Notably, composites such as TiO₂/C-550, WS₂/GO/Au, and MOF-derived α-Fe₂O₃/ZnO achieved near-complete degradation (>99%) within 30–150 min, while others, like ZnO/JSAC-COO⁻ and Ag/TiO₂/CNT, displayed enhanced charge separation and stability over five consecutive cycles. Band gap engineering (ranging from 1.7 eV to 3.2 eV) and reactive oxygen species (·OH, ·O₂⁻) generation were key to their photocatalytic performance. This review compares the structural attributes, synthetic strategies, and degradation kinetics across systems, highlighting the synergistic role of co-catalysts, surface area, and electron mobility. This work offers systematic insight into the state-of-the-art composite photocatalysts and provides a comparative framework to guide future material design for wastewater treatment applications. Full article

Titanium dioxide (TiO₂) is a benchmark photocatalyst for environmental applications, but its limited visible-light activity due to a wide band gap and fast charge recombination restricts its practical efficiency. This study presents the development of heterostructured Ag (Au)/MoS₂-TiO₂ inverse opal (IO) films that synergistically integrate photonic, plasmonic, and semiconducting functionalities to overcome these limitations. The materials were synthesized via a one-step evaporation-induced co-assembly approach, embedding MoS₂ nanosheets and plasmonic nanoparticles (Ag or Au) within a nanocrystalline TiO₂ photonic framework. The inverse opal architecture enhances light harvesting through slow-photon effects, while MoS₂ and plasmonic nanoparticles improve visible-light absorption and charge separation. By tuning the template sphere size, the photonic band gap was aligned with the TiO₂-MoS₂ absorption edge and the localized surface plasmon resonance of Ag, enabling optimal spectral overlap. The corresponding Ag/MoS₂-TiO₂ photonic films exhibited superior photocatalytic and photoelectrocatalytic degradation of tetracycline under visible light. Ultraviolet photoelectron spectroscopy and Mott–Schottky analysis confirmed favorable band alignment and Fermi level shifts that facilitate interfacial charge transfer. These results highlight the potential of integrated photonic–plasmonic-semiconductor architectures for efficient solar-driven water treatment. Full article

This work describes the application of three different AgBr heterojunctions with TiO₂, SnO₂ and WO₃ in the treatment of two water sources: wastewater from a dairy industry facility (WDI) and water from a polluted river (WPR). All heterojunctions were widely characterised, and it was observed that the physicochemical properties of all the coupled materials were similar; however, the highest elimination of Enterobacteriaceae (>90%) was obtained with the AgBr/WO₃(20%) photocatalyst in WDI. Under the same conditions, with this photocatalyst, the complete removal of bacteria (i.e., E. coli, total coliforms and other Enterobacteriaceae) was achieved in WPR. The chlorides, hardness and colour in the two water samples decreased after photocatalytic treatment with all the coupled materials. However, nitrate levels and chemical oxygen demand increased due to the possible formation of intermediary species from the photodegradation of organic pollutants and the release of metabolic intermediates from bacterial degradation during the photocatalytic process. Overall, heterogeneous photocatalysis based on AgBr-coupled materials shows potential as a tertiary treatment for WDI and for the purification of vegetable irrigation water. However, it is still important to consider the need to optimise the integrity of photocatalytic materials in order to maintain their bactericidal effectiveness through continuous reuse. Full article

The contamination of aquatic ecosystems by the micropollutants in wastewater discharges is currently a critical issue. Therefore, the development of novel treatment processes and materials is essential to ensure the availability of safe water. The present study aims to develop a photocatalytic material composed of silver nanoparticles (Ag-NPs)-doped TiO₂ supported on a Pyrex^® plate (TiO₂@Ag-NPs) exhibiting catalytic activity under visible irradiation (λ > 400 nm). The effects of Ag-NPs doping on the TiO₂ matrix, the resistance of the coating at the catalyst/substrate interface, and the photocatalytic degradation efficiency of the photocatalyst for a micropollutant (diuron) of the pesticide family were studied. The photocatalyst was characterised using X-ray diffraction, scanning electron microscopy, ultraviolet–visible spectrophotometry, and scratch tests. The solution concentrations were monitored using high-performance liquid chromatography and total organic carbon analyses. A 32% diuron removal was achieved using photocatalytic TiO₂@Ag-NPs under visible irradiation, whereas undoped TiO₂ showed no activity. Furthermore, the effects of the nanoparticle growth mode on the photocatalytic activity of TiO₂@Ag-NPs were explored. The presence of a TiO₂ sublayer ensured the adhesion of the coating and promoted the dispersion of nanoparticles within the matrix. It ensured chemical continuity (TiO₂@Ag-NPs/Pyrex^®), reduced the bandgap, and decreased electron–hole pair recombination. Full article

This study pioneers the development of a synergistic Ag-doped molecularly imprinted TiO₂ photocatalyst (MIP-Ag-TiO₂) through a multi-strategy engineering approach, integrating molecular imprinting technology with plasmonic metal modification via a precisely optimized sol–gel protocol. Breaking from conventional non-selective photocatalysts, our material features an engineered surface architecture that combines selective molecular recognition sites with enhanced charge separation capabilities, specifically tailored for the targeted degradation of recalcitrant salicylic acid (SA) contaminants. Advanced characterization (XRD, EPR, FT-IR, TEM-EDS) reveals unprecedented structure–activity relationships, demonstrating how template molecule ratios (Ti:SA = 5:1) and calcination parameters (550 °C) collaboratively optimize both adsorption selectivity and quantum efficiency. The optimized MIP-Ag-TiO₂ achieves breakthrough performance metrics: 98.6% SA degradation efficiency at 1% Ag doping, coupled with a record selectivity coefficient R = 7.128. Mechanistic studies employing radical trapping experiments identify a dual •OH/O_2⁻-mediated degradation pathway enabled by the Ag-TiO₂ Schottky junction. This work establishes a paradigm-shifting “capture-and-destroy” photocatalytic system that simultaneously addresses the critical challenges of selectivity and quantum yield limitations in advanced oxidation processes, positioning molecularly imprinted plasmonic photocatalysts as next-generation smart materials for precision water purification. Full article

TiO₂ mesoporous supports were obtained by the sol–gel method from different precursors (titaniumethoxide, isopropoxide, or butoxide) in the presence of nonionic, cationic, and anionic surfactants. Among these samples, those obtained from Ti isopropoxide, Brij58 w/o activated carbon (AC), were selected as supports. Photocatalysts were obtained by modifying these supports with Ag, Fe, and AgFe (each metal around 1% mass). The characterization results showed a stronger influence of titania precursors, surfactants, and AC on the texture and an insignificant effect on the crystalline structure and morphology of the obtained materials. X-ray photoelectron spectroscopy revealed the effects of AC and Fe on the Ag⁰ concentration and of Ag on Fe-reduced species. Based on this information, the results obtained by H₂-TPR, UV–Vis, Raman, and photoluminescence spectroscopy were explained. The performance of the photocatalysts was evaluated in the degradation of Congo Red (CR) and Crystal Violet (CV) dyes under UV and visible light. The Ag-TiO₂ sample exhibited the best activity in degrading CR at acidic pH and in degrading CV under basic conditions. In visible light, we observed the significant effects of the surface plasmon resonance, AC, Ag, and Fe on the activity in CR photodegradation. The proposed kinetics and mechanisms complete the study of the reactions. Full article

Slaughterhouses generate a huge amount of highly polluted wastewater; if left untreated, this effluent could seriously threaten the environment and human health. In the present study, Ag₂O/Ba/TiO₂ nanocomposite was synthesized using the precipitation method, and its efficacy was investigated for the remediation of real slaughterhouse wastewater (SWW) under visible light. Its performance was assessed for the inactivation of bacterial strains identified in SWW and for the degradation of total organic solids, volatile solids, fixed solids, and heavy metals. The results indicated an excellent photocatalytic performance of the synthesized Ag₂O/Ba/TiO₂ nanocomposites, confirmed by 87.3% volatile solids, 30% total organic solids, and 40% fixed solids removal from SWW. The zone of inhibition runs from 4 to 9 mm, and the nanocomposites have demonstrated outstanding bacterial inactivation activity in this range. It has been shown that the synthetic Ag₂O/Ba/TiO₂ nanocomposites can function as an effective photocatalyst for the remediation of SWW and other waste products produced by various industries worldwide. Full article

Photocatalytic H₂ production is one of the most promising approaches for sustainable energy. The literature presents a plethora of carefully designed systems aimed at harnessing solar energy and converting it into chemical energy. However, the main drawback of the reported photocatalysts is their stability. Thus, the development of a cost-effective and stable photocatalyst, suitable for real-world applications remains a challenge. An ideal photocatalyst for H₂ production must possess appropriate band-edge energy positions, an effective sacrificial agent, and a suitable cocatalyst. Among the various photocatalysts studied, TiO₂ stands out due to its stability, abundance, and non-toxicity. However, its efficiency in the visible spectrum is limited by its wide bandgap. Metal doping is an effective strategy to enhance electron–hole separation and improve light absorption efficiency, thereby boosting H₂ synthesis. Common metal cocatalysts used as TiO₂ dopants include platinum (Pt), gold (Au), copper (Cu), nickel (Ni), cobalt (Co), ruthenium (Ru), iron (Fe), and silver (Ag), as well as bimetallic combinations such as Ni-Fe, Ni-Cu, Nb-Ta, and Ni-Pt. In all cases, doped TiO₂ exhibits higher H₂ production performance compared to undoped TiO₂, as metals provide additional reaction sites and enhance charge separation. The use of bimetallic dopants further optimizes the hydrogen evolution reaction. Additionally, porphyrins, with their strong visible light absorption and efficient electron transfer properties, have demonstrated potential in TiO₂ photocatalysis. Their incorporation expands the photocatalyst’s light absorption range into the visible spectrum, enhancing H₂ production efficiency. This review paper explores the principles and advancements in metal- and porphyrin-doped TiO₂ photocatalysts, highlighting their potential for sustainable hydrogen production. Full article

To address the issue of air pollution caused by automobile exhaust in China, a titanium dioxide/graphite carbon nitride (TiO₂/g-C₃N₄) composite photocatalyst capable of degrading automobile exhaust was prepared in this study. It was used as an additive to modify styrene–-butadiene latex (SBR) emulsified asphalt. The basic properties of modified emulsified asphalt before and after aging were analyzed, and the dosage range of TiO₂/g-C₃N₄ (TCN) was determined. The environmentally friendly micro-surfacing of degradable automobile exhaust was prepared. Based on 1 h and 6 d wet wheel wear test, rutting deformation test, surface structure depth test, and pendulum friction coefficient test, the road performance of TCN environmentally friendly micro-surfacing mixture with different contents was analyzed and evaluated, and the effect of environmentally friendly degradation of automobile exhaust was studied by a self-made degradation device. The results show that when the mass ratio of TiO₂ and melamine was 1:4, the TCN composite photocatalyst had strong photocatalytic activity. The crystal structure of TiO₂ and g-C₃N₄ was not damaged during the synthesis process. The g-C₃N₄ inhibited the agglomeration of TiO₂. The introduction of N-Ti bond changed the electronic structure of TiO₂, narrowed the band gap and broadened the visible light response range. When the TCN content was in the range of 1~7%, the softening point of SBR- modified emulsified asphalt increased with the increase in TCN content, the penetration decreased, the ductility decreased gradually, and the storage stability increased gradually. The penetration ratio and ductility ratio of the composite-modified emulsified asphalt after aging increased with the increase in TCN content, and the increment of the softening point decreased. This shows that the TCN content is beneficial to the high-temperature performance and anti-aging performance of SBR-modified emulsified asphalt, and has an adverse effect on low temperature performance and storage stability. The addition of TCN can improve the wear resistance and rutting resistance of the micro-surfacing mixture, and has no effect on the water damage resistance and skid resistance. The environment-friendly micro-surfacing asphalt mixture had a significant degradation effect on NO, CO, and HC. With the increase in TCN content, the degradation efficiency of the three gases was on the rise. When the content was 5%, the degradation rates of NO, CO, and HC were 37.16%, 25.72%, and 20.44%, respectively, which are 2.34 times, 2.47, times and 2.30 times that of the 1% content, and the degradation effect was significantly improved. Full article

Solar-driven catalytic oxidation processes for the removal of toxic gaseous pollutants have attracted considerable scientific attention, and there is a strong desire to improve the mass transfer, photogenerated charge separation, and O₂ activation by regulating the structure of the photocatalyst. Initially, functionalized graphene–TiO₂ mesoporous hollow nanofibers have been controllably fabricated by a coaxial electrospinning technique, in which functionalized graphene is controllably prepared through a sequential diazonium functionalization and silane modification and ensures its uniform distribution among TiO₂ nanoparticles (NPs). Subsequently, the ultrafine Ag NPs are primarily anchored onto the surface of graphene by an in situ frozen photodeposition strategy, producing Ag/functionalized graphene–TiO₂ mesoporous hollow nanofibers (Ag/SiG-TO MPHNFs). The optimal Ag/SiG-TO MPHNFs exhibit 3.9-fold and 4.6-fold enhancements in CO photooxidation compared with TO MPHNFs and P25 TiO₂, respectively. The enhanced photoactivity can be attributed to three factors: the creation of the mesoporous hollow structure accelerates mass transfer, the incorporation of graphene facilitates the transfer of photogenerated electrons from TiO₂ to graphene, and the anchoring of Ag NPs improves O₂ activation. Full article

The introduction of oxygen vacancies (OVs) is a promising strategy to enhance the hydrogen (H₂) evolution efficiency of photocatalysts. Sodium borohydride (NaBH₄) is widely used as a reducing agent to introduce OVs, particularly in composite materials. However, its impact on H₂ evolution remains underexplored. In this study, by employing various mass ratios of NaBH₄ to P/Ag/Ag₂O/Ag₃PO₄/TiO₂ (PAgT), OVs modified PAgT (R-PAgT) composites, which were synthesized and systematically characterized by XRD, FT-IR, and XPS. R-PAgT-10 with an optimal mass ratio exhibited a superior H₂ evolution efficiency and stability, maintaining its performance over 20 cycles under visible light irradiation, while the higher mass ratio of NaBH₄/PAgT led to the disruption of the crystal structure with excessive OVs amounts, resulting in poor stability. This study highlighted the importance of utilizing the optimal mass ratio of NaBH₄ to prepare OVs-PAgT for successful and stable H₂ evolution under visible light irradiation, which holds promise for developing efficient and durable photocatalysts for renewable energy applications. Full article

TiO₂ films and N-doped TiO₂ films modified with silver (Ag/N-TiO₂) were synthesized using DC magnetron sputtering. By varying the N₂ flow rate and the Ag sputtering power, respectively, the degree of doping and modification was managed. The microstructure, morphology, and properties of the thin film were studied using X-ray diffraction, field emission scanning electron microscopy, UV visible diffuse reflectance spectroscopy, and atomic force microscopy. The results show that TiO₂ in Ag/N-TiO₂ composite has an anatase structure, and the absorption spectrum of (Ag/N-TiO₂) thin film shows a red shift. The best photocatalytic degradation effect regarding the N-TiO₂ films was observed with an N₂ flow rate of 16 sccm (standard cubic per minute). The degradation rate in MO (Methyl orange) pure solution (C₀ = 10 mg/L) can reach 100% in 85 min, and in the MO-Na₂SO₄ mixed solution (C₀ = 10 mg/L, C C_Na2SO4 = 12.5 g/L), it only takes 40 min. Ag/N-TiO₂ films exhibited the highest degradation efficiency at a 5 W sputtering power and 50 s of sputtering time, reaching a 100% degradation rate in MO pure solution that can reach 100% in 50 min, and in the MO-Na₂SO₄ mixed solution, it only takes 36 min. The photocatalytic decomposition of MO was greatly accelerated by the addition of Na₂SO₄, which worked best with a 12.5 g/L concentration. However, when the concentration of Na₂SO₄ is above or below 12.5 g/L, Na₂SO₄ exhibits significant inhibition of photocatalytic degradation. Photocatalytic cycling experiments showed that the photocatalyst still maintained an effective degradation performance after four cycles. The degradation mechanism was analyzed using first-order kinetics and energy band theory. Compared to powder particles, the photocatalyst on the films has high stability and can be recovered 100%. So, photocatalysts on films have great potential for industrial applications. Full article