Search Results (14)

Both tungsten trioxide (WO₃) nanosheet arrays and tungsten trioxide/zinc oxide (WO₃/ZnO) nanocomposites were grown on fluorine-doped tin oxide (FTO) coated glass slides using a hydrothermal method to develop a visible-light-driven photocatalyst with easy reusability. Field emission scanning electron microscopy (FE-SEM) observations confirmed the formation of irregular oxide nanosheet arrays on the FTO surfaces. X-ray diffraction (XRD) analysis revealed the presence of hexagonal WO₃ and wurtzite ZnO crystal phases. UV-Vis diffuse reflectance spectroscopy showed that integrating ZnO nanostructures with WO₃ nanosheets resulted in a blue shift of the absorption edge and a reduced absorption capacity in the visible-light region. Photoluminescence (PL) spectra indicated that the WO 0.5/ZnO 2.0 sample exhibited the lowest electron-hole recombination rate among the WO₃/ZnO nanocomposite sample. Photocatalytic degradation tests demonstrated that all WO₃/ZnO nanocomposite samples had higher photodegradation rates for a 10 ppm methylene blue (MB) aqueous solution under visible-light irradiation compared to pristine WO₃ nanosheet arrays. Among them, the WO 0.5/ZnO 2.0 sample showed the highest photocatalytic efficiency. Furthermore, it exhibited excellent recyclability and high photodegradation stability over three cycles. Full article

This study investigates the chemical and structural modifications of vertically aligned tungsten disulfide–tungsten trioxide (WS₂-WO₃) nanosheets decorated with silver nanoparticles (Ag(NPs)) under nitrogen plasma conditions. The synthesized vertically aligned WS₂-WO₃ nanosheets were functionalized through direct-current (DC) magnetron sputtering, forming silver-decorated samples. Structural changes, as well as the size and distribution of Ag(NPs), were characterized using scanning electron microscopy (SEM). Chemical state analysis was conducted via X-ray photoelectron spectroscopy (XPS), while Raman spectroscopy was employed to investigate vibrational modes. The findings confirmed the successful decoration of Ag(NPs) and identified unexpected compound transformations that were dependent on the duration of functionalization. The synthesized and functionalized samples were evaluated for their sensing capabilities towards Rhodamine B (RhB) through surface-enhanced resonance Raman scattering (SERRS). This study discusses the impact of substrate morphology and the shape and size of nanoparticles on the enhancement of SERRS mechanisms, achieving an enhancement factor (EF) of approximately 1.6 × 10⁶ and a limit of detection (LOD) of 10⁻⁹ M. Full article

Catalyzing hydrogen evolution reaction (HER) is a key process in high-efficiency proton exchange membrane water electrolysis (PEMWE) devices. To replace the use of Pt-based HER catalyst, tungsten carbide (W₂C) is one of the most promising non-noble-metal-based catalysts with low cost, replicable catalytic performance, and durability. However, the preparation access to scalable production of W₂C catalysts is inevitable. Herein, we introduced a facile protocol to achieve the tungsten carbide species by plasma treatment under a CH₄ atmosphere from the WO₃ precursor. Moreover, the heterogeneous structure of the tungsten carbide/tungsten oxide nanosheets further enhances the catalytic activity for HER with the enlarged specific surface area and the synergism on the interfaces. The prepared tungsten carbide/tungsten oxide heterostructure nanosheets (WO_3-x-850-P) exhibit exceptional HER catalytic activity and stable longevity in acid electrolytes. This work provides a facile and effective method to construct high-performance and non-precious-metal-based electrocatalysts for industrial-scale water electrolysis. Full article

Converting CO₂ greenhouse gases into high-value-added fuels via semiconductor photocatalysts is an ideal solution to address current environmental and energy issues. Due to its unique physicochemical traits and flexible structure, WO₃ is widely employed in photocatalysis. Nevertheless, it commonly faces problems such as limited light absorption and low reaction selectivity. Here, we effectively tackle the existing issue by introducing an oxygen defect strategy to synthesize two-dimensional WO_3−x nanosheets with rich oxygen vacancies. Due to localized surface plasmon resonance (LSPR), these nanosheets may exhibit broad light absorption and efficient CO₂ adsorption and activation. In the photocatalytic reduction of carbon dioxide (CO₂) to carbon monoxide (CO), WO_3−x nanosheets exhibited 100% selectivity and 16.1 μmol g⁻¹ h⁻¹ yield, 6.2 times higher than WO₃. Oxygen vacancies improve WO₃’s band structure and increase its capacity to absorb visible light. Based on electrochemical tests and fluorescence spectroscopy analysis, the outstanding functionality of WO_3−x nanosheets is related to the improved separation and transport of photocurrents and the restricted radiative recombination of the resulting electron pairs and holes. Full article

Lignin is the only renewable resource composed of aromatic hydrocarbons in nature that can be used as raw materials for preparing chemicals. However, due to the existence of stable C–O bonds and C−C bonds in the lignin, the high-value resource utilization of lignin is still challenging work. Herein, we reported efficient lignin depolymerization using a Ni-doped WO_3-x nanosheet photocatalyst that was prepared via the two-step hydrothermal treatment. The optimized catalyst (Ni-doped WO_3-x) successfully depolymerized sodium lignosulfonate to vanillic acid and guaiacol under visible-light irradiation. The active radicals of photocatalytic depolymerization of sodium lignosulfonate were superoxide radicals, photogenic holes, and hydroxyl radicals under visible-light irradiation. Furthermore, the introduction of Ni significantly decreased the activation energy barrier for selective cleavage of the C−C bond, which was the essential step to promote lactic acid production. This work presented an effective and promising strategy for lignin depolymerization and value-added biochemical production. Full article

Photocatalytic elimination of antibiotics from the environment and drinking water is of great significance for human health. However, the efficiency of photoremoval of antibiotics such as tetracycline is severely limited by the prompt recombination of electron holes and slow charge migration efficacy. Fabrication of low-dimensional heterojunction composites is an efficient method for shortening charge carrier migration distance and enhancing charge transfer efficiency. Herein, 2D/2D mesoporous WO₃/CeO₂ laminated Z-scheme heterojunctions were successfully prepared using a two-step hydrothermal process. The mesoporous structure of the composites was proved by nitrogen sorption isotherms, in which sorption-desorption hysteresis was observed. The intimate contact and charge transfer mechanism between WO₃ nanoplates and CeO₂ nanosheets was investigated using high-resolution transmission electron microscopy and X-ray photoelectron spectroscopy measurements, respectively. Photocatalytic tetracycline degradation efficiency was noticeably promoted by the formation of 2D/2D laminated heterojunctions. The improved photocatalytic activity could be attributed to the formation of Z-scheme laminated heterostructure and 2D morphology favoring spatial charge separation, confirmed by various characterizations. The optimized 5WO₃/CeO₂ (5 wt.% WO₃) composites can degrade more than 99% of tetracycline in 80 min, achieving a peak TC photodegradation efficiency of 0.0482 min⁻¹, which is approximately 3.4 times that of pristine CeO₂. A Z-scheme mechanism is proposed for photocatalytic tetracycline by from WO₃/CeO₂ Z-scheme laminated heterojunctions based on the experimental results. Full article

Herein, the heterostructure rGO-WO₃ was hydrothermally synthesized and characterized by HRTEM (high-resolution transmission electron microscopy), FESEM (field emission scanning electron microscopy), XRD (X-ray diffraction), FT-IR (Fourier transform infrared spectroscopy), XPS (X-ray photoelectron microscopy), nitrogen physisorption isotherm, Raman, TGA (thermogravimetric analysis) and zeta potential techniques. The HRTEM and FESEM images of the synthesized nanostructure revealed the successful loading of WO₃ nanorods on the surface of rGO nanosheets. The prepared heterostructure was utilized as an efficient adsorbent for the removal of a third-generation fluoroquinolone antibiotic, i.e., levofloxacin (LVX), from water. The adsorption equilibrium data were appropriately described by a Langmuir isotherm model. The prepared rGO-WO₃ heterostructure exhibited a Langmuir adsorption capacity of 73.05 mg/g. The kinetics of LVX adsorption followed a pseudo-second-order kinetic model. The adsorption of LVX onto the rGO-WO₃ heterostructure was spontaneous and exothermic in nature. Electrostatic interactions were found to have played a significant role in the adsorption of LVX onto the rGO-WO₃ heterostructure. Thus, the prepared rGO-WO₃ heterostructure is a highly promising material for the removal of emerging contaminants from aqueous solution. Full article

Background: Pathogenic microorganisms are causing increasing cases of mortality and morbidity, along with alarming rates of ineffectiveness as a result of acquired antimicrobial resistance. Bi₂WO₆ showed good potential to be used as an antibacterial substance when exposed to visible light. This study demonstrates for the first time the dimension-dependent antibacterial activity of layered Bi₂WO₆ nanosheets. Materials and methods: The synthesized layered Bi₂WO₆ nanosheets were prepared by the hydrothermal method and characterized by powder X-ray diffraction (XRD), scanning electron microscopy (SEM), atomic force microscopy (AFM), and Raman and Fourier transform infrared spectroscopy (FTIR). Antibacterial and antibiotic-modulation activities were performed in triplicate by the microdilution method associated with visible light irradiation (LEDs). Results: Bi₂WO₆ nanosheets were effective against all types of bacteria tested, with MIC values of 256 μg/mL against Escherichia coli standard and resistant strains, and 256 μg/mL and 32 μg/mL against Staphylococcus aureus standard and resistant strains, respectively. Two-dimensional (2D) Bi₂WO₆ nanosheets showed antibacterial efficiency against both strains studied without the presence of light. Conclusions: Layered Bi₂WO₆ nanosheets revealed dimension-dependent antibacterial activity of the Bi₂WO₆ system. Full article

The rational design of direct Z-scheme heterostructural photocatalysts using solar energy is promising for energy conversion and environmental remediation, which depends on the precise regulation of redox active sites, rapid spatial separation and transport of photoexcited charge and a broad visible light response. The Bi₂WO₆ materials have been paid more and more attention because of their unique photochemical properties. In this study, S²⁻ doped Bi₂WO_6-x coupled with twin crystal ZnIn₂S₄ nanosheets (Sov−BWO/T−ZIS) were prepared as an efficient photocatalyst by a simple hydrothermal method for the removal of tetracycline hydrochloride (TCH). Multiple methods (XRD, TEM, XPS, EPR, UV vis DRS, PL etc.) were employed to systematically investigate the morphology, structure, composition and photochemical properties of the as-prepared samples. The XRD spectrum indicated that the S²⁻ ions were successfully doped into the Sov−BWO component. XPS spectra and photoelectrochemical analysis proved that S²⁻ served as electronic bridge and promoted captured electrons of surface oxygen vacancies transfer to the valence band of T−ZIS. Through both experimental and in situ electron paramagnetic resonance (in situ EPR) characterizations, a defined direct Z-scheme heterojunction in S-BWO/T−ZIS was confirmed. The improved photocatalytic capability of S-BWO/T−ZIS results ascribed that broadened wavelength range of light absorption, rapid separation and interfacial transport of photoexcited charge, precisely regulated redox centers by optimizing the interfacial transport mode. Particularly, the Sov−50BWO/T−ZIS Z-scheme heterojunction exhibited the highest photodegradation rate was 95% under visible light irradiation. Moreover, this heterojunction exhibited a robust adsorption and degradation capacity, providing a promising photocatalyst for an organic pollutant synergistic removal strategy. Full article

The removal of organic pollutants using green environmental photocatalytic degradation techniques urgently need high-performance catalysts. In this work, a facile one-step hydrothermal technique has been successfully applied to synthesize a Nb₂O₅ photocatalyst with uniform micro-flower structure for the degradation of methyl orange (MO) under UV irradiation. These nanocatalysts are characterized by transmission and scanning electron microscopies (TEM and SEM), X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET) method, and UV-Vis diffuse reflectance spectroscopy (DRS). It is found that the prepared Nb₂O₅ micro-flowers presents a good crystal phases and consist of 3D hierarchical nanosheets with 400–500 nm in diameter. The surface area is as large as 48.6 m² g⁻¹. Importantly, the Nb₂O₅ micro-flowers exhibit superior catalytic activity up to 99.9% for the photodegradation of MO within 20 mins, which is about 60-fold and 4-fold larger than that of without catalysts (W/O) and commercial TiO₂ (P25) sample, respectively. This excellent performance may be attributed to 3D porous structure with abundant catalytic active sites. Full article

Bi₂WO₆ assembled by flower-like microspheres and nanosheets were controllably synthesized through a one-step hydrothermal approach. Multiple technologies, including X-ray powder diffraction (XRD), scanning electron microscopy (SEM), and UV–Vis diffuse reflectance spectrum (UV–Vis), were carried out to characterize the as-synthesized samples. The photocatalytic efficiency of Bi₂WO₆ synthesized with a series of temperature and pH values shows different morphologies and photocatalytic properties. The photocatalyst (Bi₂WO₆) synthesized at 220 °C and pH of 7 exhibited the best photocatalytic performance, with the methylene blue (MB) degradation approaching 91.6% after reaction time of 60 min. Free radical capture experiments indicate that •OH is the primary reactive species in the methylene blue (MB) degradation reaction, h⁺ and •O₂⁻ contribute negligible influence, while the addition of H₂O₂ significantly improves the photocatalytic activity of Bi₂WO₆. Biodegraded poplar preconditioning refiner chemical alkaline peroxide mechanical pulp wastewater (PPW) was treated over Bi₂WO₆ under UV light (Bi₂WO₆/UV/H₂O₂); chemical oxygen demand (COD_Cr) and color degradation rate were 85.8% and 92.0%, respectively. These results show that Bi₂WO₆ semiconductors can be introduced as an efficient and stable photocatalyst for industry wastewater treatment. Full article

The development of functionalized metal oxide/reduced graphene oxide (rGO) hybrid nanocomposites concerning power equipment failure diagnosis is one of the most recent topics. In this work, WO₃ nanolamellae/reduced graphene oxide (rGO) nanocomposites with different contents of GO (0.5 wt %, 1 wt %, 2 wt %, 4 wt %) were synthesized via controlled hydrothermal method. X-ray diffraction (XRD), transmission electron microscopy (TEM), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), thermogravimetric analyses-derivative thermogravimetric analysis-differential scanning calorimetry (TG-DTG-DSC), BET, and photoluminescence (PL) spectroscopy were utilized to investigate morphological characterizations of prepared gas sensing materials and indicated that high quality WO₃ nanolamellae were widely distributed among graphene sheets. Experimental ceramic planar gas sensors composing of interdigitated alumina substrates, Au electrodes, and RuO₂ heating layer were coated with WO₃ nanolamellae/reduced graphene oxide (rGO) films by spin-coating technique and then tested for gas sensing towards multi-concentrations of acetylene (C₂H₂) gases in a carrier gas with operating temperature ranging from 50 °C to 400 °C. Among four contents of prepared samples, sensing materials with 1 wt % GO nanocomposite exhibited the best C₂H₂ sensing performance with lower optimal working temperature (150 °C), higher sensor response (15.0 toward 50 ppm), faster response-recovery time (52 s and 27 s), lower detection limitation (1.3 ppm), long-term stability, and excellent repeatability. The gas sensing mechanism for enhanced sensing performance of nanocomposite is possibly attributed to the formation of p-n heterojunction and the active interaction between WO₃ nanolamellae and rGO sheets. Besides, the introduction of rGO nanosheets leads to the impurity of synthesized materials, which creates more defects and promotes larger specific area for gas adsorption, outstanding conductivity, and faster carrier transport. The superior gas sensing properties of WO₃/rGO based gas sensor may contribute to the development of a high-performance ppm-level gas sensor for the online monitoring of dissolved C₂H₂ gas in large-scale transformer oil. Full article

Oxygen vacancy defects play an important role in improving the light-capturing and photocatalytic activity of tungsten trioxide (WO₃). However, the hydrogen treatment method that is commonly used to introduce oxygen vacancies is expensive and dangerous. Therefore, the introduction and control of oxygen vacancy defects in WO₃ remains a challenge. Here, we demonstrated that oxygen vacancies could be successfully introduced into WO_3−x while using a facile method through low temperature annealing in alcohol. The obtained WO_3−x samples with optimal oxygen vacancies showed strong absorption of light, extending from the ultraviolet to the visible and near-infrared regions, and exhibits strong plasmon resonance from 400–1200 nm peaking at approximately 800 nm. When compared to pristine WO₃, the photocatalytic activity of WO_3−x was greatly improved in the ultraviolet and visible regions. This study provides a simple and efficient method to generate oxygen vacancies in WO₃ for photocatalysis, which may be applied in the photoelectrochemical, electrochromic, and photochromic fields. Because oxygen vacancy is a common characteristic of metal oxides, the findings that are presented herein may be extended to other metal oxides. Full article

Graphene has attracted enormous attention owing to its extraordinary properties, while graphene-based nanocomposites hold promise for many applications. In this paper, we present a two-step exploitation method for preparation of graphene oxides and a facile solvothermal route for preparation of few-layer graphene nanosheets and graphene/WO₃ nanocomposites in an ethanol-distilled water medium. The as-synthesized samples were characterized by using field emission scanning electron microscopy (FE-SEM), high-resolution transmission electron microscopy (HRTEM), ultraviolet-visible (UV-vis) spectroscopy, Raman spectroscopy, X-ray diffraction (XRD), thermogravimetric-differential thermal analysis (TG-DTA) and gas-sensing test. The resistivity of the thick-film gas sensors based on sandwich-like graphene/WO₃ nanocomposites can be controlled by varying the amount of graphene in the composites. Graphene/WO₃ nanocomposites with graphene content higher than 1% show fast response, high selectivity and fine sensitivity to NO_x. Full article