Search Results (59)

Methylene blue (MB), a widely used industrial dye, is a persistent pollutant with documented toxicity to aquatic organisms and potential health risks to humans, even at ultra-trace levels. Conventional monitoring techniques such as UV–Vis spectroscopy and fluorescence emission suffer from limited sensitivity, typically failing to detect MB below ~10⁻⁷ M. In this study, we introduce a surface-enhanced Raman spectroscopy (SERS) platform based on silver nanowire (AgNW) substrates that enables MB detection over an unprecedented dynamic range—from 1.5 × 10⁻⁴ M down to 1.5 × 10⁻¹⁶ M. Raman mapping confirmed the presence of individual signal hot spots at the lowest concentration, consistent with the theoretical number of analyte molecules in the probed area, thereby demonstrating near-single-molecule detection capability. The calculated enhancement factors reached up to 1.90 × 10¹², among the highest reported for SERS-based detection platforms. A semi-quantitative calibration curve was established spanning twelve orders of magnitude, and this platform was successfully applied to monitor MB degradation during two advanced oxidation processes (AOPs): TiO₂ nanotube-mediated photocatalysis under UV irradiation and atmospheric-pressure dielectric barrier discharge (DBD) plasma treatment. While UV–Vis and fluorescence techniques rapidly lost sensitivity during the degradation process, the SERS platform continued to detect the characteristic MB Raman peak at ~1626 cm⁻¹ throughout the entire treatment duration. These persistent SERS signals revealed the presence of residual MB or partially degraded aromatic intermediates that remained undetectable by conventional optical methods. The results underscore the ability of AgNW-based SERS to provide ultra-sensitive, molecular-level insights into pollutant transformation pathways, enabling time-resolved tracking of degradation kinetics and validating treatment efficiency. This work highlights the importance of integrating SERS with AOPs as a powerful complementary strategy for advanced environmental monitoring and water purification technologies. By delivering an ultra-sensitive, low-cost sensor (<USD 0.16 per test) and promoting reagent-free treatment methods, this study directly advances SDG 6 (Clean Water and Sanitation) and SDG 12 (Responsible Consumption and Production). Full article

Over the past two decades, the application of photocatalytic reactions in organic synthesis has increased remarkably. Porphyrins, renowned for their exceptional photophysical properties, photostability, and prevalence in natural catalytic processes, are attracting significant attention as promising photocatalysts for reactions proceeding through energy transfer and one-electron transfer. In this work, we synthesized the indium(III) complex of 2-[4-(diethoxyphosphoryl)phenyl]-1H-imidazo[4,5-b]-5,10,15,20-tetramesitylporphyrin (InTMPIP) and explored its application as a photocatalyst for the oxidation of sulfides by dioxygen or air. Complex InTMPIP was found to generate singlet oxygen with quantum yield of 0.92 (toluene) and enables efficient photooxidation of sulfides to sulfoxides by dioxygen in “green” acetonitrile/water (4:1 v/v) or methanol/chloroform (2:1 v/v) solvent mixtures with almost quantitative yield. Furthermore, InTMPIP was grafted onto hydrated mesoporous titania and materials InTMPIP/TiO₂-1 and InTMPIP/TiO₂-2 with different In/Ti ratios were obtained and investigated. The composition and structure of the materials were studied using a combination of elemental analysis, various spectroscopic methods, gas adsorption measurements, and SEM imaging. Finally, the photocatalytic efficiency of InTMPIP/TiO₂-2 was explored in aerobic photooxidation of sulfides. The heterogenized complex enables selective synthesis of sulfoxides under “green” conditions; however, it is prone to leaching into the solution when irradiated with both blue and red LEDs. Full article

Photocatalytic degradation of pollutants have a high potential for sustainable and renewable uses. TiO₂ is a widely studied photocatalyst due to its high chemical and photochemical stability and wide range of applications. However, the wide band gap and low capacity of photo-induced charge separation provide lower catalytic activity; thus, improvement of these properties must be found. The doping of TiO₂ with other elements, such as carbon nanoparticles (CNP) in a quantum dot form, offers a promising pathway to improve the aforementioned properties. In addition, in situ doping methods should be investigated for practical scalability, as they offer the advantage of integrating dopants directly during material synthesis, ensuring a more uniform distribution and better interaction between the dopant and the host material, in turn leading to more consistent photocatalytic properties. Current technologies primarily involve nanoparticle combinations. This work focuses on the development of a novel in situ synthesis methodology by the introduction of three different graphene-based quantum nanodots into anodic TiO₂ and the following investigation of structural, morphological, and photocatalytic properties. Results indicate that the introduction of CNP allows for the shift of a set of parameters, such as the optical band gap, increased photo-induced charge carrier density of TiO₂/CNP composite, and, most importantly, the change of crystalline phase composition depending on added CNP material. Research indicates that not only a higher concentration of added CNP enhances higher photocatalytic activity as tested by the degradation of methylene blue dye, but also the type of CNP determines final crystalline phase. For the first time brookite and rutile phases were obtained in anodic titania synthesized in inorganic electrolyte by introducing hydrothermally treated exfoliated graphene. Full article

A mixed metal oxide W-TiO₂ nanopowder photocatalyst was prepared by using the sol–gel method with a broad range of elemental compositions x = C_W/(C_W + C_Ti), including TiO₂ and WO₃. The material was structurally characterized and evaluated in adsorption and photocatalytic processes by testing its removal capacity of a representative pollutant methylene blue (MB) in aqueous solutions and under UV-A and sunlight illuminations. The nanopowders appeared to be more effective adsorbents than pure TiO₂ and WO₃ materials, showing a maximum at 15 mol% W, which was set as the tungsten solubility limit in anatase titania. At the same time, the photocatalytic decomposition of MB peaked at 2 mol% W. The examination of different compositions showed that the most effective MB removal took place at 15 mol% W, which was attributed to the combined action of adsorption and heterogeneous photocatalysis. Moreover, MB decomposition under sunlight was stronger than under UV-A, suggesting photocatalyst activation by visible light. The pollutant removal efficiency of the material with 15 mol% W was enhanced by a factor of ~10 compared to pure TiO₂ at the beginning of the process, which shows its high potential for use in depollution processes in emergency cases of a great pollutant leak. As a result, a W_x=0.15-TiO₂ catalyst could be of high interest for wastewater purification in industrial plants. Full article

Indium nitride is an excellent semiconductor that belongs to the group of III nitride materials. Due to its unique properties, it is applied to various optoelectronic applications. However, its low thermal stability makes it difficult to synthesize. The present study introduces the synthesis of indium nitride nanoparticles, using ultrasound power (sonochemistry). The sonochemical method provides a low-cost and rapid technique for nanomaterial synthesis. InN nanoparticles were produced in only 3 h through the sonochemical reaction of InCl₃ and LiN₃. Xylene was used as a reaction solvent. X-ray powder diffraction (XRD) as well as high-resolution transmission electron microscopy (HRTEM) were adopted for the characterization of the obtained powder. According to our results, ultrasound contributed to the synthesis of InN nanocrystals in a cubic and a hexagonal phase. The obtained InN nanoparticles were further used to decorate titanium dioxide (TiO₂) by means of ultrasound. The contribution of InN nanoparticles on the processes of photocatalysis was investigated through the degradation of methylene blue (MB), a typical organic substance acting in place of an environment pollutant. According to the obtained results, InN nanoparticles improved the photocatalytic activity of TiO₂ by 41.8% compared with commercial micrometric titania. Full article

Titania (TiO₂) nanosheets are crystals with controlled, highly ordered structures that improve the functionality of conventional TiO₂ nanoparticles. Various surface modification methods have been studied to enhance the effectiveness of these materials as photocatalysts. Surface modifications using electrical polarization have attracted considerable attention in recent years because they can improve the function of titania without changing its composition. However, the combination of facet engineering and electrical polarization has not been shown to improve the functionality of TiO₂ nanosheets. In the present study, the dye-degradation performance of polarized TiO₂ nanosheets was evaluated. TiO₂ nanosheets with a F/Ti ratio of 0.3 were synthesized via a hydrothermal method. The crystal morphology and structure were evaluated using transmission electron microscopy and X-ray diffraction. Then, electrical polarization was performed under a DC electric field of 300 V at 300 °C. The polarized material was evaluated using thermally stimulated current measurements. A dye-degradation assay was performed using a methylene blue solution under ultraviolet irradiation. The polarized TiO₂ nanosheets exhibited a dense surface charge and accelerated decolorization. These results indicate that electrical polarization can be used to enhance the photocatalytic activity of TiO₂. Full article

In this study, we investigated the preparation conditions of polystyrene (PS)@TiO₂ core–shell particles and their photocatalytic activity during the decomposition of methylene blue (MB). TiO₂ shells were formed on the surfaces of PS particles using the sol–gel method. Homogeneous PS@TiO₂ core–shell particles were obtained using an aqueous NH₃ solution as the promoter of the sol–gel reaction and stirred at room temperature. This investigation revealed that the temperature and amount of the sol–gel reaction promoter influenced the morphology of the PS@TiO₂ core–shell particles. The TiO₂ shell thickness of the PS@TiO₂ core–shell particles was approximately 5 nm, as observed using transmission electron microscopy. Additionally, Ti elements were detected on the surfaces of the PS@TiO₂ core–shell particles using energy-dispersive X-ray spectroscopy analysis. The PS@TiO₂ core–shell particles were used in MB decomposition to evaluate their photocatalytic activities. For comparison, we utilized commercial P25 and TiO₂ particles prepared using the sol–gel method. The results showed that the PS@TiO₂ core–shell particles exhibited higher activity than that of the compared samples. Full article

Focusing on the degradation of organic dyes in wastewater, a novel titania composite nanofiber small area film photocatalyst with improvedphotocatalytic activity using strontium ions and graphite as dual cocatalysts has been synthesized by electrospinning and hydrothermal methods.Morphology control, doping causing crystal defect engineering (strontium ion doping), and heterojunction building (graphite surface modification) strategies are simultaneously applied to the synthetic design of new photocatalysts.In degradation tests of rhodamine B, methyl orange, methylene blue, and malachite green, the degradation rate constants were 2.57, 2.85, 3.06, or 3.54 times higher than those of pure titania, respectively.The composite nanofiber small area film exhibited excellent recyclability in fourrecycling tests.The improved photocatalytic activity of titania composite nanofiber small area film is attributed to the morphology of the nanofibers with the addition of more reaction sites, dopingwith more crystal defects, and heterojunctions providing channels for the transfer of photogenerated carriers.Design solutions with the synergistic effects of multiple strategies inform the use of titania in industrial applications. Full article

A single-step impregnation approach is investigated as a synthetic route for photocatalyst synthesis active under visible light. The as-derived photocatalysts exhibited very high degradation rates towards methylene blue (MB) decolorization under visible light despite the high concentration of the initial MB solution concentration. The TiO₂-based photocatalysts were prepared using nitrate precursor compounds for copper and silver; thus, Ag/TiO₂ and Cu/TiO₂ photocatalysts were prepared. The photocatalyst’s physicochemical properties were determined by XRF, BET, and XRD analysis. The metal nature of the titania substrate, the titania matrix effect, and the metal concentration parameters were studied, while the catalyst concentration in the MB initial solution was optimized. Full article

This study presents a simple and sustainable coating technology for the deposition of photocatalytic coatings based on titanium dioxide and geopolymers, which requires no thermal post-treatment. Titania powder P25, potassium silicate and a calcium aluminate-based hardener were dispersed in water and applied to aluminum substrates using a paintbrush, a roller and a spray gun. The coatings were air-dried for 12 h. The photocatalytic activities were tested via degradation of an aqueous methylene blue solution in a batch reactor under artificial UV-A light. The roller and the spray gun-based coatings yielded well-adhering coatings with high photocatalytic activity. Brushed coatings were inhomogeneous and unstable. The presented method of producing photocatalytic coatings is very simple to apply and does not require complex technologies or energy-intensive thermal treatments. Full article

Solar light active photocatalyst was prepared as silver phosphate (Ag₃PO₄) coating on titania–silica (TiO₂–SiO₂) microspheres. Titania–silica microsphere was obtained by spray drying TiO₂–SiO₂ colloidal solutions, whereas Ag₃PO₄ was applied by wet impregnation. XRD on the granules and SEM analysis show that the silver phosphate particles cover the surface of the titania–silica microspheres, and UV-visible diffuse reflectance analysis highlights that Ag₃PO₄/TiO₂–SiO₂ composites can absorb the entire visible light spectrum. BET measurements show higher specific surface area of the composite samples compared to bare Ag₃PO₄. Photocatalytic activity was evaluated by dye degradation tests under solar light irradiation. The prepared catalysts follow a pseudo-first-order rate law for dye degradation tests under solar light irradiation. The composite catalysts with an Ag₃PO₄/TiO₂–SiO₂ ratio of 1:1.6 wt% show better catalytic activity towards both rhodamine B and methylene blue degradation and compared with the results with uncoated TiO₂–SiO₂ microspheres and the benchmark commercial TiO₂ (Evonik-P25) as a reference. The composite photocatalyst showed exceptional efficiency compared to its pristine counterparts and reference material. This is explained as having a higher surface area with optimum light absorption capacity. Full article

TiO₂ nanosheets have been studied as photocatalysts in various fields, and their performance has been actively improved. Herein, we prepared titania nanosheets with a smaller size than those reported previously with a side length of 29 nm and investigated their photocatalytic activity. (NH₄)₂TiF₆ and Ti(OBu)₄ were used as raw materials, and the F/Ti ratio was varied in the range of 0.3 to 2.0 to produce a series of samples with different side lengths by hydrothermal synthesis. A reduction in the F/Ti ratio led to the reduced size of the titanium nanosheets. The photocatalytic activity of each sample was evaluated through the degradation of methylene blue (MB) under ultraviolet (UV) irradiation (365 nm, 2.5 mW/cm²). UV irradiation promoted the decomposition of MB, and the highest degradation efficiency was achieved using titania nanosheets prepared with a F/Ti ratio of 0.3. The high catalytic activity can be attributed to the increase in the surface area due to size reduction. The ratio of the {001} surface exposed on the titania nanosheet also affected the photocatalytic activity; it resulted in increased activation of the reaction. This study demonstrates that further activation of the photocatalytic activity can be achieved by adjusting the size of titania nanosheets. Full article

A nanocomposite comprised of nickel titanate/titania nanoparticles decorated with carbon nanofibers (NiTiO₃/TiO₂-decorated CNFs) is successfully synthesized via electrospinning and further utilized for methylene blue (MB) photodegradation. The morphology, phase, structural and chemical composition of the nanocomposite is investigated via scanning electron microscope, X-ray diffraction and transmission electron microscope equipped with energy dispersive X-ray. A mathematical model is developed to predict the photocatalytic activity of the produced nanocomposite by considering parameters such as initial dye concentration, light intensity, reaction temperature, and catalyst dosage. The reaction rate constant K₁ decreased from 0.0153 to 0.0044 min⁻¹ with an increase in the MB concentration from 5 to 15 mg L⁻¹, while K₂, K₃, and K₄ were found to increase with the increase in reaction temperature (0.0153 to 0.0222 min⁻¹), light intensity (0.0153 to 0.0228 min⁻¹) and catalyst dose concentration (0.0153 to 0.0324 min⁻¹), respectively. The results obtained are found to be in good agreement with the modeling results and showed effective photodegradation activity. The performance of our catalyst is found to be better compared to other catalysts previously reported in the literature. The recyclability data of the synthesized NiTiO₃/TiO₂-decorated CNFs catalyst for four runs show that the catalyst is quite stable and recyclable. This nanocomposite photocatalyst offers a low-cost solution for wastewater pollution problems and opens new avenues to further explore the electrospinning method for the synthesis of nanocomposites. Full article

Simple and inexpensive electrospinning and hydrothermal techniques were used to synthesize titania nanofibers (TiO₂ NFs) (composite NFs) decorated with copper nanoparticle (Cu NPs). The fabricated composite NFs have been tested as a photocatalytic material to degrade methylene blue (MB) as a model dye under visible light. The introduced composite NFs have shown good photocatalytic activity compared with pristine TiO₂ NFs; 100% and 50% of dye were degraded in 120 min for composite NFs and pristine TiO₂ NFs, respectively. Furthermore, composite NFs demonstrated good stability for four cycles. In addition, the fabricated Cu-TiO₂ NFs have shown good photocatalytic activity for the production of H₂ from sodium borohydride. Full article

Titania is very famous photocatalyst for decomposition of organic pollutants. Its photocatalytic properties significantly depend on the morphology and chemical composition of the samples. Herein, the TiO₂ nanotubes/Cu_xO nanoheterostructures have been synthesized and the effect of heat treatment performed in molecular atmospheres of air and argon on their photoelectrochemical and photocatalytic properties has been studied. The prepared samples have a higher reaction rate constant compared to TiO₂ nanotubes in the decomposition reaction of methylene blue molecules. It is established that in argon treated nanoheterostructures, the copper oxide is present in two phases, CuO and Cu₂O, while in air treated ones there is only CuO. In the TiO₂ nanotubes/Cu_xO samples, Cu²⁺ ions and molecular O₂⁻ radicals were detected while in TiO₂ nanotubes only carbon dangling bond defects are present. The dynamics of O₂⁻ radicals under illumination are discussed. It was shown that the TiO₂ nanotubes do not exhibit photocatalytic activity under visible light. The mechanism of the photocatalytic reaction on the surface of the TiO₂ nanotubes/Cu_xO samples was proposed. It is assumed that a photocatalytic decomposition of organic molecules under visible light at the surface of the nanoheterostructures under investigation is realized mainly by the reaction of these molecules with photogenerated O₂⁻ radicals. The results obtained are completely original and indicate the high promise of the prepared photocatalysts. Full article