Flake-like InVO4 modified TiO2 nanofibers with longer carrier lifetimes for visible-light photocatalysts

Highly efficient solar light absorption capabilities and quantum yields in photocatalysts are key to their application in photocatalytic fields. Towards this end, TiO₂/InVO₄ nanofibers (NFs) have been designed and fabricated successfully by a one-pot electrospinning process. The resulting TiO₂/InVO₄ NFs display excellent visible-light photocatalytic activity, owing to their prominent visible-light absorption and electron–hole separation properties. Time-resolved transient PL spectroscopy demonstrated that the TiO₂/InVO₄ NFs display longer emission decay times (22.0 ns) compared with TiO₂ NFs (15.5 ns), implying that the heterojunction can remarkably suppress the electron–hole recombination and promote the carrier transfer efficiency. With tailored heterostructure features, TiO₂/InVO₄ NFs exhibit superior visible-light photodegradation activity, and after 80 min of visible-light irradiation, almost 95% of RhB molecules can be decomposed by TiO₂/InVO₄ NFs, while only 18% of RhB molecules can be decomposed by pure TiO₂ NFs.

TiO₂/InVO₄ nanofibers have been designed and fabricated successfully by one-pot electrospinning process, which display longer carrier lifetime (22 ns) and enhanced visible-light photocatalytic activity.     

Enhanced photocatalytic activity of a B12-based catalyst co-photosensitized by TiO2 and Ru(ii) towards dechlorination

A novel hybrid photocatalyst denoted as B₁₂–TiO₂–Ru(ii) was prepared by co-immobilizing a B₁₂ derivative and trisbipyridine ruthenium (Ru(bpy)₃²⁺) on the surface of a mesoporous anatase TiO₂ microspheres and was characterized by DRS, XRD, SEM and BET et al. By using the hybrid photocatalyst, DDT was completely didechlorinated and a small part of tridechlorinated product was also detected in the presence of TEOA only after 30 min of visible light irradiation. Under simulated sunlight, the hybrid exhibited a significantly enhanced photocatalytic activity for dechlorination compared with B₁₂–TiO₂ under the same condition or itself under visible light irradiation due to the additivity in the contribution of UV and visible part of the sunlight to the electron transfer. In addition, this hybrid catalyst can be easily reused without loss of catalytic efficiency. This is the first report on a B₁₂-based photocatalyst co-sensitized by two photosensitizers with wide spectral response.

The additivity of the contribution of the UV and visible parts of sunlight to electron transfer was confirmed in the B₁₂–TiO₂–Ru(ii) photocatalytic system.     

A novel multifunctional Ag and Sr2+ co-doped TiO2@rGO ternary nanocomposite with enhanced p-nitrophenol degradation,and bactericidal and hydrogen evolution activity

In the present study, a novel multifunctional Sr²⁺/Ag–TiO₂@rGO ternary hybrid photocatalyst was prepared via facile sol–gel and hydrothermal methods. The prepared catalyst was well characterized by UV-vis, XRD, Raman, HRTEM and XPS. The synthesized composite was utilised for p-NP degradation, E. coli disinfection and H₂ generation under visible light. The Sr²⁺/Ag–TiO₂@rGO catalyst showed enhanced photocatalytic H₂ evolution rate (64.3 μmol h⁻¹) compared with Ag–TiO₂@rGO (30.1 μmol h⁻¹) and TiO₂ (no activity). Nearly complete degradation of 15 mg l⁻¹p-NP was achieved over Sr²⁺/Ag–TiO₂@rGO after 3 h, while only 66% and 5% was achieved by Ag–TiO₂@rGO and TiO₂ respectively. Furthermore, TEM analysis was carried out on Escherichia coli (E. coli) before and after visible light irradiation to understand the inactivation mechanism and DNA analysis indicated no fragmentation during inactivation. Radical quantification experiments and ESR analysis suggested that ·OH and O₂˙⁻ were the main ROS in the degradation and disinfection processes. The superior photocatalytic H₂ evolution rate of Sr²⁺/Ag–TiO₂@rGO was attributed to the synergetic effect between the Ag, Sr²⁺ and TiO₂ components on the rGO surface. The localized SPR effect of Ag induced visible light generated charge carriers into the conduction band of the TiO₂ and Sr²⁺ which further transfer to the rGO for the reduction of H⁺ ions into H₂. The results suggest that Sr²⁺/Ag–TiO₂@rGO structures could not only induce separation and migration efficiency of charge carries, but also improve charge collection efficiency for enhanced catalytic activity. Thus, we believe that this work could provide new insights into multifunctional nanomaterials for applications in solar photocatalytic degradation of harmful organics and pathogenic bacteria with clean energy generation during wastewater treatment.

In the present study, a novel multifunctional Sr²⁺/Ag–TiO₂@rGO ternary hybrid photocatalyst was prepared via facile sol–gel and hydrothermal methods.     

TiO2–Au composite nanofibers for photocatalytic hydrogen evolution

TiO₂-based materials for photocatalytic hydrogen (H₂) evolution have attracted much interest as a renewable approach for clean energy applications. TiO₂–Au composite nanofibers (NFs) with an average fiber diameter of ∼160 nm have been fabricated by electrospinning combined with calcination treatment. In situ reduced gold nanoparticles (NPs) with uniform size (∼10 nm) are found to disperse homogenously in the TiO₂ NF matrix. The TiO₂–Au composite NFs catalyst can significantly enhance the photocatalytic H₂ generation with an extremely high rate of 12 440 μmol g⁻¹ h⁻¹, corresponding to an adequate apparent quantum yield of 5.11% at 400 nm, which is 25 times and 10 times those of P25 (584 μmol g⁻¹ h⁻¹) and pure TiO₂ NFs (1254 μmol g⁻¹ h⁻¹), respectively. Furthermore, detailed studies indicate that the H₂ evolution efficiency of the TiO₂–Au composite NF catalyst is highly dependent on the gold content. This work provides a strategy to develop highly efficient catalysts for H₂ evolution.

The H₂ production rate of TiO₂–Au nanofibers is dramatically improved to 12 440 μmol g⁻¹ h⁻¹, 10 times that of pure TiO₂.     

Enhanced visible-light photodegradation of fluoroquinolone-based antibiotics and E. coli growth inhibition using Ag–TiO2 nanoparticles

Antibiotics in wastewater represent a growing and worrying menace for environmental and human health fostering the spread of antimicrobial resistance. Titanium dioxide (TiO₂) is a well-studied and well-performing photocatalyst for wastewater treatment. However, it presents drawbacks linked with the high energy needed for its activation and the fast electron–hole pair recombination. In this work, TiO₂ nanoparticles were decorated with Ag nanoparticles by a facile photochemical reduction method to obtain an increased photocatalytic response under visible light. Although similar materials have been reported, we advanced this field by performing a study of the photocatalytic mechanism for Ag–TiO₂ nanoparticles (Ag–TiO₂ NPs) under visible light taking in consideration also the rutile phase of the TiO₂ nanoparticles. Moreover, we examined the Ag–TiO₂ NPs photocatalytic performance against two antibiotics from the same family. The obtained Ag–TiO₂ NPs were fully characterised. The results showed that Ag NPs (average size: 23.9 ± 18.3 nm) were homogeneously dispersed on the TiO₂ surface and the photo-response of the Ag–TiO₂ NPs was greatly enhanced in the visible light region when compared to TiO₂ P25. Hence, the obtained Ag–TiO₂ NPs showed excellent photocatalytic degradation efficiency towards the two fluoroquinolone-based antibiotics ciprofloxacin (92%) and norfloxacin (94%) after 240 min of visible light irradiation, demonstrating a possible application of these particles in wastewater treatment. In addition, it was also proved that, after five Ag–TiO₂ NPs re-utilisations in consecutive ciprofloxacin photodegradation reactions, only a photocatalytic efficiency drop of 8% was observed. Scavengers experiments demonstrated that the photocatalytic mechanism of ciprofloxacin degradation in the presence of Ag–TiO₂ NPs is mainly driven by holes and ˙OH radicals, and that the rutile phase in the system plays a crucial role. Finally, Ag–TiO₂ NPs showed also antibacterial activity towards Escherichia coli (E. coli) opening the avenue for a possible use of this material in hospital wastewater treatment.

Ag nanoparticles decorated-TiO₂ P25 are a viable alternative for the degradation, through a rutile-mediated mechanism, of fluoroquinolone-based antibiotics under visible light irradiation and, at the same time, for bacteria inactivation in water.     

Rational design of a polypyrrole-based competent bifunctional magnetic nanocatalyst

The combination of conducting polymers with semiconductors for the fabrication of organic/inorganic hybrid nanocatalysts is one of the most promising research areas for many applications. In this work, the synthesized nanocomposite combines several advantages such as the photoresponse shift from the UV region toward visible light by narrowing the band gap of the semiconductor, magnetic separation ability and dual applications including the catalytic reduction of p-nitrophenol (PNP) and the photocatalytic degradation of methylene blue (MB) dye. In addition to the core magnetite nanoparticles (NPs), the synthesized nanocomposite contains polypyrrole (PPY) and TiO₂ shells that are decorated with silver metal NPs to prevent electron–hole recombination and to enhance the catalytic performance. Indeed, the catalytic PNP reduction experiments reveal that the synthesized nanocomposite exhibits significantly high catalytic activity with a rate constant of 0.1169 min⁻¹. Moreover, the photocatalytic experiments show that the synthesized nanophotocatalyst has a boosting effect toward MB dye degradation under normal daytime visible light irradiation with a rate constant of 6.38 × 10⁻² min⁻¹. The synergetic effect between silver NPs, PPY and TiO₂ is thought to play a fundamental role in enhancing the photocatalytic activity.

An efficient method to synthesize a magnetic nanocomposite with dual catalytic activities with a synergetic effect between Ag nanoparticles, polypyrrole and TiO₂ is described.     

Enhanced charge separation in TiO2/nanocarbon hybrid photocatalysts through coupling with short carbon nanotubes

The interfacial contact between TiO₂ and graphitic carbon in a hybrid composite plays a critical role in electron transfer behavior, and in turn, its photocatalytic efficiency. Herein, we report a new approach for improving the interfacial contact and delaying charge carrier recombination in the hybrid by wrapping short single-wall carbon nanotubes (SWCNTs) on TiO₂ particles (100 nm) via a hydration-condensation technique. Short SWCNTs with an average length of 125 ± 90 nm were obtained from an ultrasonication-assisted cutting process of pristine SWCNTs (1–3 μm in length). In comparison to conventional TiO₂–SWCNT composites synthesized from long SWCNTs (1.2 ± 0.7 μm), TiO₂ wrapped with short SWCNTs showed longer lifetimes of photogenerated electrons and holes, as well as a superior photocatalytic activity in the gas-phase degradation of acetaldehyde. In addition, upon comparison with a TiO₂–nanographene “quasi-core–shell” structure, TiO₂-short SWCNT structures offer better electron-capturing efficiency and slightly higher photocatalytic performance, revealing the impact of the dimensions of graphitic structures on the interfacial transfer of electrons and light penetration to TiO₂. The engineering of the TiO₂–SWCNT structure is expected to benefit photocatalytic degradation of other volatile organic compounds, and provide alternative pathways to further improve the efficiency of other carbon-based photocatalysts.

The interfacial contact between TiO₂ and graphitic carbon in a hybrid composite plays a critical role in electron transfer behavior, and in turn, its photocatalytic efficiency.     

A new Ru(ii) polypyridyl complex as an efficient photosensitizer for enhancing the visible-light-driven photocatalytic activity of a TiO2/reduced graphene oxide nanocomposite for the degradation of atrazine: DFT and mechanism insights

TiO₂ is one of the most widely used semiconductors for photocatalytic reactions. However, its wide bandgap energy and fast charge recombination limit its catalytic activity. Thus, herein, a new Ru(ii) polypyridyl complex, [Ruii(tptz)(CH₃CN)Cl₂] (tptz = 2,4,6-tris(2-pyridyl)-1,3,5-triazine), was synthesized and used as a visible-light photosensitizer dye for improving the light harvesting and quantum efficiency of TiO₂. Accordingly, a well-designed nanostructured photocatalyst was proposed using mesoporous TiO₂ nanocrystals coupled with reduced graphene oxide (rGO) and the polypyridyl Ru(ii) complex, which was tested for the photocatalytic degradation of atrazine (ATZ) as a model of emerging water contaminants. Specifically, the Ru complex (Ru-CMP) served as an electron donor, while rGO acted as an electron acceptor, and the synergistic effect between them promoted the separation of electron–hole pairs and suppressed the charge recombination in the hybridized species. Structural analysis indicated that the TiO₂ nanoparticles with an anatase crystal structure had a mesoporous texture and were homogeneously coated on the rGO sheets. The detailed FT-IR, Raman, XPS and UV-vis absorption spectroscopic analyses combined with EDS mapping clearly confirmed the successful loading of the Ru complex onto the catalyst. The PL and EIS results revealed that the addition of the Ru-CMP photosensitizer enhanced the charge separation and transport. The gas-phase geometry and energies of the molecular orbitals of the Ru complex were evaluated via DFT calculations. The results from the DFT calculations were consistent with the experimental results. Compared to pure TiO₂, the as-synthesized Ru-CMP-TiO₂/rGO hybrid exhibited significantly enhanced photocatalytic activity for the degradation of ATZ. The rate of ATZ degradation in the developed photocatalytic process with the Ru-CMP-TiO₂/rGO hybrid was 9 times that with commercial TiO₂. The enhanced photocatalytic activity of the prepared catalyst can be attributed to its better light harvesting and efficient electron transportation due to its more suitable LUMO position than the conduction band of TiO₂. Moreover, the excellent conductivity and adsorption capacity of graphene contributed to the increase in photocatalytic activity. Thus, these features make the Ru-CMP-TiO₂/rGO hybrid nanomaterial an excellent candidate for the photocatalytic purification of contaminated water.

TiO₂ is one of the most widely used semiconductors for photocatalytic reactions.     

Multifunctional Ag-decorated g-C3N4 nanosheets as recyclable SERS substrates for CV and RhB detection

In this study, g-C₃N₄/Ag hybrid nanostructures were fabricated by facilely decorating silver nanoparticles on atmosphere-treated g-C₃N₄ and served as efficient SERS-active substrates. The observed significant SERS enhancement of crystal violet (CV) molecules on g-C₃N₄/Ag could be attributed to the high ability to concentrate target molecules through π–π stacking interactions and the near-field enhancement caused by the boosting SPR effect of the Ag NPs. The atmosphere and calcination time have a considerable impact on the SERS enhancement effect of the g-C₃N₄/Ag substrate. Furthermore, it took only 10 min to degrade dye molecules under visible light, and after 6 cycles the g-C₃N₄/Ag substrates still maintained sensitive SERS activity. This research indicates that g-C₃N₄/Ag hybrids can be applied as reusable SERS substrates.

In this study, g-C₃N₄/Ag hybrid nanostructures were fabricated by facilely decorating silver nanoparticles on atmosphere-treated g-C₃N₄ and served as efficient SERS-active substrates.     

Molecular imprinting on PtPd nanoflowers for selective recognition and determination of hydrogen peroxide and glucose

PtPd nanoflowers (PtPd NFs) exhibit intrinsic peroxidase-like activity as nanozymes, but the nanozymes lack substrate specificity and have low catalytic activity. Herein, a molecularly imprinted nanogel on PtPd NFs was prepared by using 3,3′,5,5′-tetramethylbenzidine (TMB) as the template through the aqueous precipitation polymerization method. After the TMB was washed out, many substrate binding pockets were retained in the PtPd NFs. Scanning electron microscopy (SEM), transmission electron microscopy (TEM) and powder X-ray diffraction (XRD) were employed to characterize the molecularly imprinted polymer (MIP) PtPd nanoflowers (T-MIP-PtPd NFs). The obtained T-MIP-PtPd NFs exhibited enhanced catalytic activity and specific recognition for TMB. Compared with PtPd NFs, T-MIP-PtPd NFs showed a linear range from 0.01–5000 μM and a detection limit of 0.005 μM toward the detection of H₂O₂. Glucose can also be sensitively detected through cascade reaction by the T-MIP-PtPd NFs and glucose oxidase. Therefore, molecular imprinting on nanozymes technology shows promising application in biocatalysis and sensing fields.

PtPd nanoflowers (PtPd NFs) exhibit intrinsic peroxidase-like activity as nanozymes, but the nanozymes lack substrate specificity and have low catalytic activity.     

The effect of heat treatment on the anatase–rutile phase transformation and photocatalytic activity of Sn-doped TiO2 nanomaterials

Sn-doped TiO₂ nanomaterials with different amounts of Sn (1, 2.5, 5, 10, and 15 at%) were prepared by a sol–gel method and characterized by XRD, TG, DTA, EDS, XPS, DRS, SEM, BET, and PL. The photocatalytic activity of the prepared samples was investigated by measuring the degradation of rhodamine B in aqueous solution under UV light. The experimental results indicate that doping with Sn promotes phase transformation from anatase to rutile. The photocatalytic activity of TiO₂ is influenced by both the heat treatment temperature and the Sn doping concentration. 1% Sn–TiO₂ exhibits the highest degradation rate at 350 °C and 5% Sn–TiO₂ exhibits the best photocatalytic activity at 500 °C and 650 °C. The enhancement of the photocatalytic activity can be ascribed to a larger surface area and a better hydration ability, as well as less recombination of the photogenerated pairs.

Sn incorporation into TiO₂ lattices promotes anatase/rutile transformation and Sn–TiO₂ exhibits better photocatalytic activity at different temperatures.     

Efficient photocatalysis with graphene oxide/Ag/Ag2S–TiO2 nanocomposites under visible light irradiation

Lack of visible light response and low quantum yield hinder the practical application of TiO₂ as a high-performance photocatalyst. Herein, we present a rational design of TiO₂ nanorod arrays (NRAs) decorated with Ag/Ag₂S nanoparticles (NPs) synthesized through successive ion layer adsorption and reaction (SILAR) and covered by graphene oxide (GO) at room temperature. Ag/Ag₂S NPs with uniform sizes are well-dispersed on the TiO₂ nanorods (NRs) as evidenced by electron microscopic analyses. The photocatalyst GO/Ag/Ag₂S decorated TiO₂ NRAs shows much higher visible light absorption response, which leads to remarkably enhanced photocatalytic activities on both dye degradation and photoelectrochemical (PEC) performance. Its photocatalytic reaction efficiency is 600% higher than that of pure TiO₂ sample under visible light. This remarkable enhancement can be attributed to a synergy of electron-sink function and surface plasmon resonance (SPR) of Ag NPs, band matching of Ag₂S NPs, and rapid charge carrier transport by GO, which significantly improves charge separation of the photoexcited TiO₂. The photocurrent density of GO/Ag/Ag₂S–TiO₂ NRAs reached to maximum (i.e. 6.77 mA cm⁻²vs. 0 V). Our study proves that the rational design of composite nanostructures enhances the photocatalytic activity under visible light, and efficiently utilizes the complete solar spectrum for pollutant degradation.

The photocatalytic reaction efficiency of GO/Ag/Ag₂S–TiO₂ nanorod arrays is 600% higher than that of a pure TiO₂ sample under visible light.     

Significant improvement in TiO2 photocatalytic activity through controllable ZrO2 deposition

ZrO₂ was deposited on anatase TiO₂ nanoparticles using 5–80 cycles of atomic layer deposition (ALD). The photocatalytic activity of all samples was evaluated based on the degradation of methylene blue (MB) solution under UV light. The TiO₂ sample with 45 cycles of ZrO₂ deposition (45c-Zr/TiO₂, 1.1 wt% ZrO₂) was proved to be the most efficient catalyst with a degradation kinetic constant 10 times larger than that of the pure TiO₂ sample. All samples were characterized using inductively coupled plasma atomic emission spectroscopy (ICP-AES), nitrogen adsorption–desorption, X-ray diffraction (XRD), transmission electron microscopy (TEM), UV-vis diffuse reflectance spectra analysis (UV-DRS), Raman and photoluminescence (PL) techniques. The high photocatalytic activity of 45c-Zr/TiO₂ can be attributed to stronger adsorption in the ultraviolet region and a reduction in the recombination rate of electron/hole pairs.

The photocatalytic activity of ZrO₂ deposited anatase TiO₂ nanoparticles was evaluated based on the degradation of methylene blue solution under UV light.     

Mesoporous hollow black TiO2 with controlled lattice disorder degrees for highly efficient visible-light-driven photocatalysis

Black TiO₂ has received tremendous attention because of its lattice disorder-induced reduction in the TiO₂ bandgap, which yields excellent light absorption and photocatalytic ability. In this report, a highly efficient visible-light-driven black TiO₂ photocatalyst was synthesized with a mesoporous hollow shell structure. It provided a higher specific surface area, more reaction sites and enhanced visible light absorption capability, which significantly promoted the photocatalytic reaction. Subsequently, the mesoporous hollow black TiO₂ with different lattice disorder-engineering degrees were designed. The structure disorder in the black TiO₂ obviously increased with reduction temperature, leading to improved visible light absorption. However, their visible-light-driven photocatalytic efficiency increased first and then decreased. The highest value can be observed for the sample reduced at 350 °C, which was 2-, 1.4- and 5-fold that of the samples reduced at 320 °C, 380 °C and 400 °C, respectively. This contradiction can be ascribed to the varied functions of the surface defects with different concentrations in the black TiO₂ during the catalytic process. In particular, the defects at low concentrations boost photocatalysis but reverse photocatalysis at high concentrations when they act as charge recombination centers. This study provides significant insight for the fabrication of high-efficiency visible-light-driven catalytic black TiO₂ and the understanding of its catalysis mechanism.

Our work provides significant insights into the design of hollow black TiO₂ spheres and the mechanism accounting for their high-efficient visible-light-driven catalysis.     

Unbiased spontaneous solar hydrogen production using stable TiO2–CuO composite nanofiber photocatalysts

We report on the optimization of electrospun TiO₂–CuO composite nanofibers as low-cost and stable photocatalysts for visible-light photocatalytic water splitting. The effect of different annealing atmospheres on the crystal structure of the fabricated nanofibers was investigated and correlated to the photocatalytic activity of the material. The presence of CuO resulted in narrowing the bandgap of TiO₂ and shifting the absorption edge into the visible region of the light spectrum. The effect of incorporating CuO within TiO₂ nanofibers on the crystal structure and composition was also investigated using X-ray diffraction (XRD), electron paramagnetic resonance (EPR), and X-ray photoelectron spectroscopy (XPS) techniques. The fabricated TiO₂–CuO composite nanofibers showed 117% enhancement in the amount of hydrogen evolved during the photocatalytic water splitting process compared to pure TiO₂. This enhancement was related to the created shallow defect states that facilitate charge transfer from TiO₂ to CuO and distinct characteristics of the composite nanofibers, such as the high surface area and directional charge transfer. The study showed that Cu is a promising alternative to noble metals as a catalyst in photocatalytic water splitting, with the advantage of being an Earth abundant element and a relatively cheap material.

We report on the optimization of electrospun TiO₂–CuO composite nanofibers as low-cost and stable photocatalysts for visible-light photocatalytic water splitting.     

Goethite–titania composite: disinfection mechanism under UV and visible light

Goethite–titania (α-FeOOH–TiO₂) composites were prepared by co-precipitation and mechanical milling. The structural, morphological and optical properties of as-synthesized composites were characterized by X-ray powder diffraction, scanning electron microscopy and UV-Vis diffuse reflectance spectroscopy, respectively. α-FeOOH–TiO₂ composites and TiO₂-P25, as reference, were evaluated as photocatalysts for the disinfection of Escherichia coli under UV or visible light in a stirred tank reactor. α-FeOOH–TiO₂ exhibited better photocatalytic activity in the visible region than TiO₂-P25. The mechanical activation increased the absorption in the visible range of TiO₂-P25 and the photocatalytic activity of α-FeOOH–TiO₂. In the experiments with UV light and α-FeOOH–TiO₂, mechanically activated, a 5.4 log-reduction of bacteria was achieved after 240 min of treatment. Using visible light the α-FeOOH–TiO₂ and the TiO₂-P25 showed a 3.1 and a 0.7 log-reductions at 240 min, respectively. The disinfection mechanism was studied by ROS detection and scavenger experiments, demonstrating that the main ROS produced in the disinfection process were superoxide radical anion, singlet oxygen and hydroxyl radical.

A photocatalytic mechanism for FeOOH–TiO₂ composite is proposed under UV-Vis light, the FeOOH–TiO₂ composite showed higher photocatalytic activity than TiO₂-P25.     

Efficient detoxification of triclosan by a S–Ag/TiO2@g-C3N4 hybrid photocatalyst: process optimization and bio-toxicity assessment

Owing to their persistency and toxicity, development of an effective strategy to eliminate antibiotic residues from the aquatic system has become a major environmental concern. Doping TiO₂ with hetero atoms and forming a hybrid structure with g-C₃N₄ could serve as an efficient visible light active photocatalytic candidate. In this study, a novel S–Ag/TiO₂@g-C₃N₄ hybrid catalyst was prepared for visible light degradation and detoxification of triclosan (TS) antibiotic. The effect of various operational parameters towards the photocatalytic degradation was systematically evaluated through response surface methodology (RSM) based on central composite design (CCD). The highest TS degradation (92.3%) was observed under optimal conditions (TS concentration = 10 mg L⁻¹, pH = 7.8, and catalyst weight = 0.20 g L⁻¹) after 60 min. Efficient charge separation resulted from the doped nanoparticles (silver and sulphur), the existing integrated electric field of the heterojunction and the overlying light response of hybridized TiO₂ and g-C₃N₄, thus the S–Ag/TiO₂@g-C₃N₄ composite showed impressively higher activity. The main degradation products of TS were identified by LC/ESI-MS analysis. In addition, the toxicity of the degradation products was investigated through an Escherichia coli (E. coli) colony forming unit assay and the results revealed that under optimal conditions a significant reduction in biotoxicity was noticed.

Owing to their persistency and toxicity, development of an effective strategy to eliminate antibiotic residues from the aquatic system has become a major environmental concern.     

Mechanistic pathways for the degradation of SMX drug and floatation of degraded products using F–Pt co-doped TiO2 photocatalysts

This work presents smart pathways to enhance the photocatalytic activity of TiO₂via co-doping with fluorine (F) and platinum (Pt) to form F–Pt co-doped TiO₂ photocatalysts and investigates the unique and unusual fluorination of the floated products. Our investigations indicate that the crystalline structure of the photocatalysts was a mixture of anatase and brookite phases and that the nanoparticles of the synthesized nanocomposites had nanometric sizes (4–25 nm). The F–Pt co-doped TiO₂ nano-photocatalysts demonstrated degradation of sulfamethoxazole (SMX) drug of >93% within 90 min under direct solar light and 58% degradation within 360 min under a solar simulator. Thus, co-doping TiO₂ with F and Pt atoms to form F–Pt co-doped TiO₂ nanocomposite is an efficient pathway to achieve high photocatalytic performance escorted with the formation of floating metal-fluoropolymer, unlike pristine TiO₂ which has less photocatalytic degradation and no generation of a floating polymer. Our photocatalytic protocol demonstrates that the degradation of SMX started with redox reactions of oxygen and water absorbed on the surface of the prepared nanocomposites to form superoxide anions (O₂˙⁻) and hydroxy radicals (˙OH) which have oxidation superpower. The resultant products were subsequently fluorinated by fluoride radical ions and floated as metal-fluoropolymer.

This work presents smart pathways to enhance the photocatalytic activity of TiO₂via co-doping with fluorine (F) and platinum (Pt) to form F–Pt co-doped TiO₂ photocatalysts and investigates the unique and unusual fluorination of the floated products.     

N/Fe/Zn co-doped TiO2 loaded on basalt fiber with enhanced photocatalytic activity for organic pollutant degradation

To avoid the loss of catalytic material powder, a loaded catalytic material of TiO₂ with basalt fiber as the carrier (TiO₂@BF) was synthesized by an improved sol–gel method. The TiO₂@BF was doped with different contents of N, Fe and Zn elements and was used to degrade rhodamine B (RhB) under ultraviolet light. The physical characterization analysis indicated that the co-doping of the N, Fe and Zn elements had the effects of reducing grain size, increasing sample surface area, and narrowing the electronic band gap. The electronic band gap of nitrogen–iron–zinc co-doped TiO₂@BF (N/Fe/Zn_TiO₂@BF) was 2.80 eV, which was narrower than that of TiO₂@BF (3.11 eV). The degradation efficiency of RhB with N/Fe/Zn_TiO₂@BF as a photocatalyst was 4.3 times that of TiO₂@BF and its photocatalytic reaction was a first-order kinetic reaction. Quenching experiments suggested that the reactive species mainly include photoinduced holes (h⁺), superoxide radicals (˙O₂⁻) and hydroxyl radicals (˙OH). In brief, this study provides a prospective loaded catalytic material and routine for the degradation of organic contaminants in water by a photocatalytic process.

The photocatalytic activity of N/Fe/Zn_TiO₂@BF, synthesized by a combined sol–gel calcination method, showed great improvement for the degradation of RhB. The reaction mechanism of N/Fe/Zn_TiO₂@BF for the degradation of RhB was proposed.     

Highly effective photocatalytic performance of {001}-TiO2/MoS2/RGO hybrid heterostructures for the reduction of Rh B

Effective separation and rapid transfer of photogenerated electron–hole pairs are key features of photocatalytic materials with high catalytic activity, which could be achieved in co-catalysts. It is reported that the two-dimensional (2D) MoS₂ is a promising co-catalyst due to its unique semi-conductive properties and graphene-like layered structure. However, the application of MoS₂ as a co-catalyst is limited by its poor electrical conductivity. On the other hand, it is worth noting that TiO₂ possesses reactive crystal facets, which is one of the dominant mechanisms for the separation of photogenerated electron–hole pairs. In this work, we prepared MoS₂/RGO hybrids as co-catalysts which were doped to TiO₂ with highly reactive {001} planes via the hydrothermal method. It was found that the {001}-TiO₂/MoS₂/RGO photocatalysts with 7 wt% MoS₂/RGO co-catalyst show the highest photodegradation activity for the degradation of Rh B under visible light irradiation (λ > 400 nm), which could result from the synergy of the effective separation of electron–hole pairs by the {001} facets in TiO₂ and the rapid transfer of electron–hole pairs in MoS₂/RGO. The results show that the {001}-TiO₂/MoS₂/RGO hybrid is a low-cost and stable photocatalyst for the effective degradation of Rh B under visible light.

Effective separation and rapid transfer of photogenerated electron–hole pairs are key features of photocatalytic materials with high catalytic activity, which could be achieved by co-catalysts.