Search Results (171)

TiO₂ is the most used material for the photocatalytic removal of organic pollutants in aqueous media. TiO₂, specifically its anatase phase, is well-known for its great performance under UV irradiation, high chemical stability, low cost and non-toxicity. Nevertheless, TiO₂ presents two main drawbacks: its limited absorption of the visible spectrum; and its relatively low specific surface area and pore volume. Regarding the latter, several works in the literature have addressed the issue by developing new synthesis approaches in which anatase is dispersed and supported on the surface of porous materials. In the present work, two series of materials have been prepared where anatase has been supported on mesoporous silica (MSTiR%) in situ through a hydrothermal synthesis approach, where, in addition to using tetraethoxysilane (TEOS) as a silicon precursor, three organotriethoxysilanes [RTEOS, where R = methyl (M), propyl (P) or phenyl (Ph)] were used at a RTEOS:TEOS molar percentage of 10 and 30%. The materials were thoroughly characterized by several techniques to determine their morphological, textural, chemical, and UV-vis light absorption properties and then the most promising materials were used as photocatalysts in the photodegradation of the emerging contaminant and antiepileptic carbamazepine (CBZ) under UV irradiation. The materials synthesized using 10% molar percentage of RTEOS (MSTiR10) were able to almost completely degrade (~95%), 1 mg L⁻¹ of CBZ after 1 h of irradiation using a 275 nm LED and 0.5 g L⁻¹ of catalyst dose. Therefore, this new synthesis approach has proven useful to develop photoactive TiO₂ composites with enhanced textural properties. Full article

This work explores the influence of material properties and experimental conditions on both biological and photocatalytic nitrate reduction processes. For the biological route, results demonstrate that carbon supports, specifically carbon gels, with open porosity, slight acidity, and high purity enhance E. coli adhesion and promote the formation of highly active bacterial colonies. However, carbon supports of bacteria, produced from waste biomass, emerge as a sustainable and cost-effective alternative, improving scalability and environmental value. The complete conversion of nitrates to nitrites, followed by full nitrite reduction, is achieved under optimized conditions. Photocatalytic nitrate reduction under solar radiation is also proposed as a promising and ecofriendly upgrade method to conventional wastewater treatment. Graphene oxide (GO) was used to enhance the photocatalytic activity of TiO₂ nanoparticles for the degradation of nitrates. The efficiency of nitrate reduction is found to be highly sensitive to solution pH and the physicochemical nature of the photocatalyst surface, which governs nitrate interactions through electrostatic forces. TiO₂–GO composites achieved up to 80% nitrate removal within 1 h and complete removal of 50 mg/L nitrate within 15 min under optimized conditions. The screening of hole scavengers revealed that formic acid, in combination with the TiO₂–GO composite, delivered exceptional performance, achieving complete nitrate reduction in just 15 min under batch conditions at an acidic pH. Full article

Artificial intelligence (AI), when integrated with photocatalysis, has demonstrated high predictive accuracy in optimizing photocatalytic processes for wastewater treatment using a variety of catalysts such as TiO₂, ZnO, CdS, Zr, WO₂, and CeO₂. The progress of research in this area is greatly enhanced by advancements in data science and AI, which enable rapid analysis of large datasets in materials chemistry. This article presents a comprehensive review and critical assessment of AI-based supervised learning models, including support vector machines (SVMs), artificial neural networks (ANNs), and tree-based algorithms. Their predictive capabilities have been evaluated using statistical metrics such as the coefficient of determination (R²), root mean square error (RMSE), and mean absolute error (MAE), with numerous investigations documenting R² values greater than 0.95 and RMSE values as low as 0.02 in forecasting pollutant degradation. To enhance model interpretability, Shapley Additive Explanations (SHAP) have been employed to prioritize the relative significance of input variables, illustrating, for example, that pH and light intensity frequently exert the most substantial influence on photocatalytic performance. These AI frameworks not only attain dependable predictions of degradation efficiency for dyes, pharmaceuticals, and heavy metals, but also contribute to economically viable optimization strategies and the identification of novel photocatalysts. Overall, this review provides evidence-based guidance for researchers and practitioners seeking to advance wastewater treatment technologies by integrating supervised machine learning with photocatalysis. Full article

Improving air quality is a significant environmental challenge. This research explored the potential of asphalt mixtures functionalized with a chitosan–TiO₂ composite (CS-TiO₂) to reduce high NO₂ concentrations and improve durability. For the assessment of the photocatalytic efficiency of the new CS-TiO₂ composite, a low-cost reactor adapted to accommodate asphalt Marshall-type specimens and high pollutant concentrations encompassing a passive sampling module was developed. The CS-TiO₂ was synthesized using a wet impregnation method at a concentration of 2%, and asphalt mixtures were treated with aqueous solutions of the photocatalysts at 2.5 g/m² and 5.0 g/m². Laboratory tests using the photocatalytic reactor and passive sampling of NO₂ revealed pollutant reductions of 21% with TiO₂ and 28% with CS-TiO₂. CS-TiO₂ achieved 15% efficiency in visible light, reducing NO₂ levels and offering UV protection to the asphalt mixtures. Additionally, the chitosan improved the photocatalyst’s adhesion by about 18%, as confirmed by tape test results, suggesting enhanced durability on pavement surfaces. The results achieved showcase the relevance of the proposed methodological improvements for supporting further research. Full article

Improving the efficiency of photocatalysts for hydrogen production while minimizing the amount of noble metals used is a pressing issue in modern green energy. This study examines the effect of ultra-small Pt additives on increasing the efficiency of the CuO_x-dark TiO₂ photocatalyst used in the hydrogen evolution reaction (HER). Initially, Pt was photoreduced from the hydroxonitrate complex (Me₄N)₂[Pt₂(OH)₂(NO₃)₈] onto the surface of nanodispersed CuO_x powder obtained by pulsed laser ablation. Then, the obtained Pt-CuO_x particles were dispersed on the surface of highly defective dark TiO₂, so that the mass content of Pt in the samples varied in the range from 1.25 × 10⁻⁵ to 10⁻⁴. The prepared samples were examined using HRTEM, XRD, XPS, and UV-Vis DRS methods. It has been established that in the Pt-CuO_x particles, platinum is mainly present in the form of single atoms (SAs), both as Pt²⁺ (predominantly) and Pt⁴⁺ species, which should facilitate electron transfer and contribute to the manifestation of the strong metal–support interaction (SMSI) effect between SA Ptⁿ⁺ and CuO_x. In turn, in the Pt-CuO_x-dark TiO₂ samples, surface defects (O_v) and surface OH groups on dark TiO₂ particles act as “anchors”, promoting the spontaneous dispersion of CuO_x in the form of sub-nanometer clusters with the reduction of Cu²⁺ to Cu¹⁺ when localized near such O_v defects. During photocatalytic HER in aqueous glycerol solutions, irradiation was found to initiate a large number of catalytically active Pt⁰-CuO_x-O_v-dark TiO₂ centers, where the SMSI effect causes electron transfer from titania to SA Pt, thus promoting better separation of photogenerated charges. As a result, ultra-small additives of Pt led to up to a 1.34-fold increase in the amount of released hydrogen, while the maximum apparent quantum yield (AQY) reached 65%. Full article

Photocatalysis offers a cost-effective and eco-friendly approach for environmental remediation, yet traditional powdered photocatalysts suffer from poor recyclability and separation challenges. To address these limitations, we developed a recyclable carbon fiber-supported composite photocatalyst (CC/TiO₂ NRs@MoS₂ NPs) featuring a three-dimensional hierarchical core–shell architecture. This structure comprises a TiO₂ seed layer, vertically aligned TiO₂ nanorod arrays as the core, and a MoS₂ nanoparticle shell, fabricated via sequential deposition. Under simulated solar irradiation, the TiO₂@MoS₂ heterojunction exhibited significantly enhanced uranium adsorption capacity, achieving a remarkable 97.3% photocatalytic removal efficiency within 2 h. At an initial uranium concentration of 200 ppm, the material demonstrated an exceptional extraction capacity of 976.7 mg g⁻¹, outperforming most reported photocatalysts. These findings highlight the potential of this 3D core–shell design for efficient uranium recovery and environmental purification applications. Full article

This study presents the development of Cu-doped NiMo/TiO₂ photoelectrocatalysts for simultaneous green hydrogen production and pharmaceutical pollutant removal under simulated solar irradiation. The catalysts were synthesized via wet impregnation (15 wt.% total metal loading with 0.6 wt.% Cu) and thermally treated at 400 °C and 900 °C to investigate structural transformations and catalytic performance. Comprehensive characterization (XRD, BET, SEM, XPS) revealed phase transitions, enhanced crystallinity, and redistribution of redox states upon Cu incorporation, particularly the formation of NiTiO₃ and an increase in oxygen vacancies. Crystallite sizes for anatase, rutile, and brookite ranged from 21 to 47 nm at NiMoCu400, while NiMoCu900 exhibited only the rutile phase with 55 nm crystallites. BET analysis showed a surface area of 44.4 m²·g⁻¹ for NiMoCu400, and electrochemical measurements confirmed its higher electrochemically active surface area (ECSA, 2.4 cm²), indicating enhanced surface accessibility. In contrast, NiMoCu900 exhibited a much lower BET surface area (1.4 m²·g⁻¹) and ECSA (1.4 cm²), consistent with its inferior photoelectrocatalytic performance. Compared to previously reported binary NiMo/TiO₂ systems, the ternary NiMoCu/TiO₂ catalysts demonstrated significantly improved hydrogen production activity and more efficient photoelectrochemical degradation of paracetamol. Specifically, NiMoCu400 showed an anodic peak current of 0.24 mA·cm⁻² for paracetamol oxidation, representing a 60% increase over NiMo400 and a cathodic current of −0.46 mA·cm⁻² at −0.1 V vs. RHE under illumination, nearly six times higher than the undoped counterpart (–0.08 mA·cm⁻²). Mott–Schottky analysis further revealed that NiMoCu400 retained n-type behavior, while NiMoCu900 exhibited an unusual inversion to p-type, likely due to Cu migration and rutile-phase-induced realignment of donor states. Despite its higher photosensitivity, NiMoCu900 showed negligible photocurrent, confirming that structural preservation and surface redox activity are critical for photoelectrochemical performance. This work provides mechanistic insight into Cu-mediated photoelectrocatalysis and identifies NiMoCu/TiO₂ as a promising bifunctional platform for integrated solar-driven water treatment and sustainable hydrogen production. Full article

Sorption and advanced oxidative processes (AOPs) are potential strategies for the removal of organic compounds, such as caffeine, from aqueous media. Such strategies tend to be more promising when combined with biopolymeric membranes as sorbents and photocatalyst supports. Therefore, the aim of the present study was to investigate sorption and AOP parameters in the performance of chitosan membranes and chitosan/TiO₂ composite membranes in individual and hybrid systems involving the photolysis, photocatalysis, and sorption of caffeine. Caffeine degradation by photolysis was 19.51 ± 1.14, 28.61 ± 0.05, and 30.64 ± 6.32%, whereas caffeine degradation by photocatalysis with catalytic membrane was 18.33 ± 2.20, 20.83 ± 1.49, and 31.41 ± 3.08% at pH 6, 7, and 8, respectively. In contrast, photocatalysis with the dispersed catalyst achieved degradation of 93.56 ± 2.12, 36.42 ± 2.59, and 31.41 ± 1.07% at pH 6, 7, and 8, respectively. These results indicate that ions present in the buffer solutions affect the net electrical charge on the surface of the composite biomaterial with the change in pH variation, occupying active sorption sites in the structure of the biomaterial, which was characterized by Fourier transform infrared spectrometry, thermogravimetric analysis, differential scanning thermogravimetry, and X-ray diffraction. Thus, it is verified that in a combined process of caffeine removal under UV irradiation and use of chitosan/TiO₂ composite membranes in phosphate-buffered medium, the photolysis mechanism is predominant, with little or no contribution from sorption, and that the TiO₂ catalyst promotes a significant reduction in the percentage of pollutant in the medium only when used dispersed and at low pH. Full article

TiO₂ was synthesized via the sol–gel method and employed as a support material for the deposition of CdS nanofibers using two novel techniques: impregnation and photodeposition. XRD characterization shows that crystallite size decreases when CdS is incorporated into TiO₂. UV-Vis spectroscopy showed that the bandgap of the CdS/TiO₂ heterostructured nanocomposites decreases compared to the raw TiO₂ support, making them very appropriate for photocatalytic applications in the visible region. The photocatalysts were tested for hydrogen production in methanol–water solutions under visible light conditions. It was observed that the TiC20 photocatalyst prepared by the impregnation method improved the photocatalytic activity compared with photodeposition technique (TiC20FD), achieving a maximum hydrogen production of 570.5 µmol H₂ ${\mathrm{g}}_{\mathrm{c}\mathrm{a}\mathrm{t}}^{-1}$ h⁻¹, while the latter attained 383.4 µmol H₂ ${\mathrm{g}}_{\mathrm{c}\mathrm{a}\mathrm{t}}^{-1}$ h⁻¹. Full article

Titanium dioxide (TiO₂) is a wide-bandgap semiconductor material with broad application potential, known for its excellent photocatalytic performance, high chemical stability, low cost, and non-toxicity. These properties make it highly attractive for applications in photovoltaic energy, environmental remediation, and optoelectronic devices. For instance, TiO₂ is widely used as a photocatalyst for hydrogen production via water splitting and for degrading organic pollutants, thanks to its efficient photo-generated electron–hole separation. Additionally, TiO₂ exhibits remarkable performance in dye-sensitized solar cells and photodetectors, providing critical support for advancements in green energy and photoelectric conversion technologies. Boron-doped diamond (BDD) is renowned for its exceptional electrical conductivity, high hardness, wide electrochemical window, and outstanding chemical inertness. These unique characteristics enable its extensive use in fields such as electrochemical analysis, electrocatalysis, sensors, and biomedicine. For example, BDD electrodes exhibit high sensitivity and stability in detecting trace chemicals and pollutants, while also demonstrating excellent performance in electrocatalytic water splitting and industrial wastewater treatment. Its chemical stability and biocompatibility make it an ideal material for biosensors and implantable devices. Research indicates that the combination of TiO₂ nanostructures and BDD into heterostructures can exhibit unexpected optical and electrical performance and transport behavior, opening up new possibilities for photoluminescence and rectifier diode devices. However, applications based on this heterostructure still face challenges, particularly in terms of photodetector, photoelectric emitter, optical modulator, and optical fiber devices under high-temperature conditions. This article explores the potential and prospects of their combined heterostructures in the field of optoelectronic devices such as photodetector, light emitting diode (LED), memory, field effect transistor (FET) and sensing. TiO₂/BDD heterojunction can enhance photoresponsivity and extend the spectral detection range which enables stability in high-temperature and harsh environments due to BDD’s thermal conductivity. This article proposes future research directions and prospects to facilitate the development of TiO₂ nanostructured materials and BDD-based heterostructures, providing a foundation for enhancing photoresponsivity and extending the spectral detection range enables stability in high-temperature and high-frequency optoelectronic devices field. Further research and exploration of optoelectronic devices based on TiO₂-BDD heterostructures hold significant importance, offering new breakthroughs and innovations for the future development of optoelectronic technology. Full article

Nano-titanium dioxide (TiO₂) is currently the most widely studied photocatalyst. However, its rapid recombination of photogenerated carriers and narrow range of light absorption have limited its development. Crystal form regulation and polymer modification are important means for improving the photocatalytic activity of single-phase materials. In this paper, TiO₂ materials of different crystal forms were prepared by changing the synthesis conditions, and they were compounded with trimesoyl chloride–melamine polymers (TMPs) by the hydrothermal synthesis method. Then, their photocatalytic performance was evaluated by degrading methylene blue (MB) under visible light. The mechanisms of influence of TiO₂ crystal form on the photocatalytic activity of TiO₂-TMP were explored by combining characterization and theoretical calculation. The results showed that the TiO₂ crystal form, through interface interaction, the built-in electric field intensity of the heterojunction, and active sites, affected the interface charge separation and transfer, thereby influencing the photocatalytic activity of TiO₂-TMP. In the 4T-TMP photocatalytic system, the degradation rate of MB was the highest. These studies provide theoretical support for understanding the structure–property relationship of the interfacial electronic coupling between TiO₂ crystal forms and TMP, as well as for developing more efficient catalysts for pollutant degradation. 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

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

In this study, a Bi₂O₃-TiO₂/PAC ternary composite photocatalyst was successfully synthesized via a hydrothermal method, employing powdered activated carbon (PAC) as the support and using bismuth nitrate and tetrabutyl titanate as raw materials. The external morphology, microstructure, elemental composition, and optoelectronic properties of the catalyst were characterized by XRD, SEM, TEM, XPS, UV-Vis DRS, and BET analyses. The photocatalytic activity of the composite toward the degradation of malachite green (MG) was systematically evaluated under various conditions. The results revealed that the composite exhibited excellent photocatalytic activity, achieving a degradation efficiency of up to 99%. Apart from extremely acidic or alkaline conditions, MG removal efficiency increased with a rising solution pH. Moreover, the photocatalyst exhibited excellent adaptability and stability in the presence of coexisting inorganic anions and humic substances, indicating its broad potential for practical applications. Reactive-species-trapping experiments indicated that superoxide radicals (·O₂⁻) were the primary active species in the degradation process, with hydroxyl radicals (·OH) and photogenerated holes (h⁺) acting synergistically. Moreover, the catalyst maintained over 90% removal efficiency after five consecutive cycles, demonstrating its excellent stability and reusability. This work provides a promising strategy and theoretical foundation for the efficient photocatalytic treatment of MG-contaminated wastewater. Full article

Antibiotic residues in the marine environment pose a serious threat to ecosystems and human health, and there is an urgent need to develop efficient and selective pollution control technologies. Molecular imprinting technology (MIT) provides a new idea for antibiotic pollution control with its specific recognition and targeted removal ability. However, traditional titanium dioxide (TiO₂) photocatalysts have limited degradation efficiency and lack of selectivity for low concentrations of antibiotics. This paper reviews the preparation strategy and modification means of molecularly imprinted TiO₂ (MI-TiO₂) and its composites and systematically explores its application mechanism and performance advantages in marine antibiotic wastewater treatment. It was shown that MI-TiO₂ significantly enhanced the selective degradation efficiency of antibiotics such as tetracyclines and sulfonamides through the enrichment of target pollutants by specifically imprinted cavities, combined with the efficient generation of photocatalytic reactive oxygen species (ROS). In addition, emerging technologies such as magnetic/electric field-assisted catalysis and photothermal synergistic effect further optimized the recoverability and stability of the catalysts. This paper provides theoretical support for the practical application of MI-TiO₂ in complex marine pollution systems and looks forward to its future development in the field of environmental remediation. Full article