Search Results (38)

Due to its persistence and potential negative effects on ecosystems and human health, microplastic pollution in aquatic environments has become a major worldwide concern. Photocatalytic degradation is a sustainable manner to degrade microplastics to non-toxic by-products. In this review, comprehensive discussion focuses on the synergistic effects of various photocatalytic materials including TiO₂, ZnO, WO₃, graphene oxide, and metal–organic frameworks for producing heterojunctions and involving multidimensional nanostructures. Such mechanisms can include the generation of reactive oxygen species and polymer chain scission, which can lead to microplastic breakdown and mineralization. The advancements of material modifications in the (nano)structure of photocatalysts, doping, and heterojunction formation methods to promote UV and visible light-driven photocatalytic activity is discussed in this paper. Reactor designs, operational parameters, and scalability for practical applications are also reviewed. Photocatalytic systems have shown a lot of development but are hampered by shortcomings which include a lack of complete mineralization and production of intermediary secondary products; variability in performance due to the fluctuation in the intensity of solar light, limited UV light, and environmental conditions such as weather and the diurnal cycle. Future research involving multifunctional, environmentally benign photocatalytic techniques—e.g., doped composites or composite-based catalysts that involve adsorption, photocatalysis, and magnetic retrieval—are proposed to focus on the mechanism of utilizing light effectively and the environmental safety, which are necessary for successful operational and industrial-scale remediation. Full article

Photoelectrochromic devices, which combine light-induced color change with energy-efficient optical modulation, have attracted significant attention for applications such as smart windows, displays, and optical sensors. However, achieving high optical modulation, fast switching speeds, and long-term stability remains a major challenge. In this study, we explore the structural and photoelectrochromic enhancements in tungsten oxide (WO₃) films achieved by doping with molybdenum disulfide quantum dots (MoS₂ QDs) and grapheneoxide–molybdenum disulfide quantum dots (GO–MoS₂ QDs) for advanced photoelectrochromic devices. X-ray diffraction (XRD) analysis revealed that doping with MoS₂ QDs and GO–MoS₂ QDs leads to a reduction in the crystallite size of WO₃, as evidenced by the broadening and decrease in peak intensity. Transmission Electron Microscopy (TEM) confirmed the presence of characteristic lattice fringes with interplanar spacings of 0.36 nm, 0.43 nm, and 0.34 nm, corresponding to the planes of WO₃, MoS₂, and graphene. Energy-Dispersive X-ray Spectroscopy (EDS) mapping indicated a uniform distribution of tungsten, oxygen, molybdenum, and sulfur, suggesting homogeneous doping throughout the WO₃ matrix. Scanning Electron Microscopy (SEM) analysis showed a significant decrease in film thickness from 724.3 nm for pure WO₃ to 578.8 nm for MoS₂ QD-doped WO₃ and 588.7 nm for GO–MoS₂ QD-doped WO₃, attributed to enhanced packing density and structural reorganization. These structural modifications are expected to enhance photoelectrochromic performance by improving charge transport and mechanical stability. Photoelectrochromic performance analysis showed a significant improvement in optical modulation upon incorporating MoS₂ QDs and GO–MoS₂ QDs into the WO₃ matrix, achieving a coloration depth of 56.69% and 70.28% at 630 nm, respectively, within 10 min of 1.5 AM sun illumination, with more than 90% recovery of the initial transmittance within 7 h in dark conditions. Additionally, device stability was improved by the incorporation of GO–MoS₂ QDs into the WO₃ layer. The findings demonstrate that incorporating MoS₂ QDs and GO–MoS₂ QDs effectively modifies the structural properties of WO₃, making it a promising material for high-performance photoelectrochromic applications. Full article

The NiWO₄ powder was prepared by combining the hydrothermal method with calcination. Several studies have demonstrated that the NiWO₄/graphene oxide composite can enhance the electrochemical performance of the NiWO₄ material. However, no studies have investigated the use of NiWO₄/graphene oxide composite material as the cathode material in zinc-ion batteries. The successful preparation of the NiWO₄/graphene oxide composite material is verified by various characterization techniques. The NiWO₄/graphene oxide composite, which is meant to be a cathode material, is fabricated into electrode sheets and incorporated into CR2025 coin cells for electrochemical assessment. The experimental results indicate that the material exhibits a high charge–discharge specific capacity with high rates. At a current density of 0.1 A g⁻¹, it has a specific capacity of 490.2 mA h g⁻¹. Even after 2000 charge–discharge cycles at a current density of 1 A g⁻¹, the capacity remains constant at 75.2%. Through calculations, it is found that the charge storage is mainly contributed to by pseudocapacitance. Full article

The present study investigates the effect of different concentrations of Na₂WO₄ and graphene oxide dispersed composite additives on the structure and corrosion resistance of 6063 aluminum alloy micro-arc oxidation (MAO) coatings in a silicate electrolyte. The characterisation of the microstructure, cross-sectional morphology, elemental distribution, and phase composition of the films was conducted utilising scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS), and X-ray diffraction (XRD). The corrosion resistance of the films was tested by prolonged immersion for 24 h, 72 h, 168 h, and 240 h, with measurement of kinetic potential polarisation curves and impedance modulus in a 3.5 wt.% NaCl solution. The densification of the films was enhanced with increasing mass concentration of Na₂WO₄ and dispersed graphene oxide in the electrolyte, and the thickness initially increased and then decreased. The film containing 6 g of Na₂WO₄ and 10 mL of graphene oxide dispersion (G10-6) exhibited optimal densification and thickness, with an I_corr value of 3.01 × 10⁻⁶ A·cm⁻² and a low-frequency impedance film value of 10⁸ Ω·cm², thereby demonstrating the most advanced corrosion resistance among the films. The densification and corrosion resistance of the films were enhanced by the incorporation of Na₂WO₄ and graphene oxide dispersion into the alkaline electrolyte. Full article

Water pollution with phenolic compounds is a serious environmental issue that can pose a major threat to the water sources. This pollution can come from various agricultural and industrial activities. Phenolic compounds can have detrimental effects on both human health and the environment. Therefore, it is essential to develop and improve analytical methods for determination of these compounds in the water samples. In this work, the aim was to design and develop an electrochemical sensing platform for the determination of 2,4-dichlorophenol (2,4-DCP) in water samples. In this regard, a nanocomposite consisting of CoWO₄ nanoparticles (NPs) anchored on reduced graphene oxide nanosheets (rGO NSs) was prepared through a facile hydrothermal method. The formation of the CoWO₄/rGO nanocomposite was confirmed via different characterization techniques. Then, the prepared CoWO₄/rGO nanocomposite was used to modify the surface of a screen-printed carbon electrode (SPCE) for enhanced determination of 2,4-DCP. The good electrochemical response of the modified SPCE towards the oxidation of 2,4-DCP was observed by using cyclic voltammetry (CV) due to the good properties of CoWO₄ NPs and rGO NSs along with their synergistic effects. Under optimized conditions, the CoWO₄/rGO/SPCE sensor demonstrated a broad linear detection range (0.001 to 100.0 µM) and low limit of detection (LOD) (0.0007 µM) for 2,4-DCP determination. Also, the sensitivity of CoWO₄/rGO/SPCE for detecting 2,4-DCP was 0.3315 µA/µM. In addition, the good recoveries for determining spiked 2,4-DCP in the water samples at the surface of CoWO₄/rGO/SPCE showed its potential for determination of this compound in real samples. Full article

This study presents the fabrication and characterization of chemoresistive sensors based on a nanocomposite of WO3-Pt and graphene for methane detection. The graphene was prepared using a liquid-phase exfoliation technique, and the nanocomposite was deposited onto interdigitated gold electrodes using drop-casting. The response of the sensors was analyzed by measuring changes in electrical resistance at methane concentrations of 7, 5, 3, and 1 ppm. Full article

Rapid industrialization and urbanization are the two significant issues causing environmental pollution. The polluted water from various industries contains refractory organic materials such as dyes. Heterogeneous photocatalysis using semiconductor metal oxides is an effective remediation technique for wastewater treatment. In this research, we used a co-precipitation-assisted hydrothermal method to synthesize a novel I-FeWO₄/GO sunlight-active nanocomposite. Introducing dopant reductive iodine species improved the catalytic activity of FeWO₄/GO. I⁻ ions improved the catalytic performance of H₂O₂ by doping into FeWO₄/GO composite. Due to I⁻ doping and the introduction of graphene as a support medium, enhanced charge separation and transfer were observed, which is crucial for efficient heterogeneous surface reactions. Various techniques, like FTIR, SEM-EDX, XRD, and UV–Vis spectroscopy, were used to characterize composites. The Tauc plot method was used to calculate pristine and iodine-doped FeWO₄/GO bandgap. Iodine doping reduced the bandgap from 2.8 eV to 2.6 eV. The degradation of methylene blue (MB) was evaluated by optimizing various parameters like catalyst concentration, oxidant dose, pH, and time. The optimum conditions for photocatalysts where maximum degradation occurred were pH = 7 for both FeWO₄/GO and I-FeWO₄/GO; oxidant dose = 9 mM and 7 mM for FeWO₄/GO and I-FeWO₄/GO; and catalyst concentration = 30 mg and 35 mg/100 mL for FeWO₄/GO and I-FeWO₄/GO; the optimum time was 120 min. Under these optimum conditions, FeWO₄/GO and I-FeWO₄/GO showed 92.0% and 97.0% degradation of MB dye. Full article

With the unprecedented development of green and renewable energy sources, the proportion of clean hydrogen (H₂) applications grows rapidly. Since H₂ has physicochemical properties of being highly permeable and combustible, high-performance H₂ sensors to detect and monitor hydrogen concentration are essential. This review discusses a variety of fiber-optic-based H₂ sensor technologies since the year 1984, including: interferometer technology, fiber grating technology, surface plasma resonance (SPR) technology, micro lens technology, evanescent field technology, integrated optical waveguide technology, direct transmission/reflection detection technology, etc. These technologies have been evolving from simply pursuing high sensitivity and low detection limits (LDL) to focusing on multiple performance parameters to match various application demands, such as: high temperature resistance, fast response speed, fast recovery speed, large concentration range, low cross sensitivity, excellent long-term stability, etc. On the basis of palladium (Pd)-sensitive material, alloy metals, catalysts, or nanoparticles are proposed to improve the performance of fiber-optic-based H₂ sensors, including gold (Au), silver (Ag), platinum (Pt), zinc oxide (ZnO), titanium oxide (TiO₂), tungsten oxide (WO₃), Mg₇₀Ti₃₀, polydimethylsiloxane (PDMS), graphene oxide (GO), etc. Various microstructure processes of the side and end of optical fiber H₂ sensors are also discussed in this review. Full article

Hydrogen (H₂) is a renewable energy source that has the potential to reduce greenhouse gas emissions. However, H₂ is also highly flammable and explosive, requiring sensitive and safe sensors for its detection. This work presents the synthesis and characterization of WO₃/graphene binary and WO₃/graphene/Pd (WG-Pd) ternary nanocomposites with varying graphene and Pd contents using the microwave-assisted hydrothermal method. The excellent catalytic efficacy of Pd nanoparticles facilitated the disintegration of hydrogen molecules into hydrogen atoms with heightened activity, consequently improving the gas-sensing properties of the material. Furthermore, the incorporation of graphene, possessing high conductivity, serves to augment the mobility of charge carriers within the ternary materials, thereby expediting the response/recovery rates of gas sensors. Both graphene and Pd nanoparticles, with work functions distinct from WO₃, engender the formation of a heterojunction at the interface of these diverse materials. This enhances the efficacy of electron–hole pair separation and further amplifies the gas-sensing performance of the ternary materials. Consequently, the WG-Pd based sensors exhibited the best gas-sensing performance when compared to anther materials, such as a wide range of hydrogen concentrations (0.05–4 vol.%), a short response time and a good selectivity below 100 °C, even at room temperature. This result indicates that WG-Pd ternary materials are a promising room-temperature hydrogen-sensing materials for H₂ detection. Full article

Environmental and human health are seriously threatened by organic dye pollution. Many efforts have been made to find effective and safe methods of eliminating these contaminants. To mitigate these effects, the hydrothermal method was used to effectively generate a ternary kind of Dy₂WO₆-ZnO embedded in graphene oxide (DWZG) nanocomposites, which were used to degrade the pollutant. Powder X-ray diffraction (XRD) investigation confirms the crystalline character of the as-prepared DWZG nanocomposite. The Dy₂WO₆-ZnO composition on the graphene oxide (GO) layer is shaped like a combination of algae (Dy₂WO₆) and clusters (ZnO), as shown by scanning electron microscopy (SEM). X-ray photoelectron spectroscopy (XPS) investigation revealed the composition of elements and oxidation state of C, Dy, O, W and Zn elements. Methylene blue (MB) was chosen as the organic dye target for photocatalytic degradation using the produced nanocomposites. MB is degraded with a photocatalytic efficiency of 98.2% in about 30 min using a DWZG catalyst. Based on the result of the research entitled “Reactive Oxidative Species,” the primary reactive species involved in the MB degradation are photo-generated ^•OH and O₂^•− radicals. The recycle test was also successful in evaluating the catalysts’ long-term viability as well as their reusability. Full article

For applications involving water cleanup, metal oxide nanoparticles are exceptionally successful. They are useful for the adsorption and photocatalytic destruction of organic pollutants due to their distinctive qualities, which include their wide surface/volume area, high number of active sites, porous structure, stability, recovery, and low toxicity. Metal oxide nanomaterials have drawn a lot of attention from researchers in the past ten years because of their various production pathways, simplicity in surface modification, abundance, and inexpensive cost. A wide range of metal oxides, such as iron oxides, MgO, TiO₂, ZnO, WO₃, CuO, Cu₂O, metal oxides composites, and graphene–metal oxides composites, with variable structural, crystalline, and morphological features, are reviewed, emphasizing the recent development, challenges, and opportunities for adsorptive removal and photocatalytic degradation of organic pollutants such as dyes, pesticides, phenolic compounds, and so on. In-depth study of the photocatalytic mechanism of metal oxides, their composites, and photocatalytically important characteristics is also covered in this paper. Metal oxides are particularly effective photocatalysts for the degradation of organic pollutants due to their high photodegradation efficiency, economically sound methods for producing photo-catalytic materials, and precise band-gap engineering. Due to their detrimental effects on human health, pesticides—one of the highly hazardous organic pollutants—play a significant part in environmental contamination. Depending on where they come from and who they are targeting, they are categorized in various ways. Researchers focusing on metal oxides and their composites for the adsorptive and photocatalytic degradation of pesticides would find the review to be a beneficial resource. Detailed information on many pesticides, difficulties associated with pesticides, environmental concentration, and the necessity of degradation has been presented. Full article

In this study tungsten oxide and graphene oxide (GO-WO_2.89) were successfully combined using the ultra-sonication method and embedded with polyphenylsulfone (PPSU) to prepare novel low-fouling membranes for ultrafiltration applications. The properties of the modified membranes and performance were investigated using Fourier-transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), contact angle (CA), water permeation flux, and bovine serum albumin (BSA) rejection. It was found that the modified PPSU membrane fabricated from 0.1 wt.% of GO-WO_2.89 possessed the best characteristics, with a 40.82° contact angle and 92.94% porosity. The permeation flux of the best membrane was the highest. The pure water permeation flux of the best membrane showcased 636.01 L·m⁻²·h⁻¹ with 82.86% BSA rejection. Moreover, the membranes (MR-2 and MR-P2) manifested a higher flux recovery ratio (FRR %) of 92.66 and 87.06%, respectively, and were less prone to BSA solution fouling. The antibacterial performance of the GO-WO_2.89 composite was very positive with three different concentrations, observed via the bacteria count method. These results significantly overtake those observed by neat PPSU membranes and offer a promising potential of GO-WO_2.89 on activity membrane performance. Full article

Two-dimensional graphene oxide (GO)-based lamellar membranes have been widely developed for desalination, water purification, gas separation, and pervaporation. However, membranes with a well-organized multilayer structure and controlled pore size remain a challenge. Herein, an easy and efficient method is used to fabricate MoO₂@GO and WO₃@GO nanocomposite membranes with controlled structure and interlayer spacing. Such membranes show good separation for salt and heavy metal ions due to the intensive stacking interaction and electrostatic attraction. The as-prepared composite membranes showed high rejection rates (˃70%) toward small metal ions such as sodium (Na⁺) and magnesium (Mg²⁺) ions. In addition, both membranes also showed high rejection rates ˃99% for nickel (Ni²⁺) and lead (Pb²⁺) ions with good water permeability of 275 ± 10 L m⁻² h⁻¹ bar⁻¹. We believe that our fabricated membranes will have a bright future in next generation desalination and water purification membranes. Full article

Transition metal oxide nanostructures are promising materials for energy storage devices, exploiting electrochemical reactions at nanometer solid–liquid interface. Herein, WO₃ nanorods and hierarchical urchin-like nanostructures were obtained by hydrothermal method and calcination processes. The morphology and crystal phase of WO₃ nanostructures were investigated by scanning and transmission electron microscopy (SEM and TEM) and X-ray diffraction (XRD), while energy storage performances of WO₃ nanostructures-based electrodes were evaluated by cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD) tests. Promising values of specific capacitance (632 F/g at 5 mV/s and 466 F/g at 0.5 A/g) are obtained when pure hexagonal crystal phase WO₃ hierarchical urchin-like nanostructures are used. A detailed modeling is given of surface and diffusion-controlled mechanisms in the energy storage process. An asymmetric supercapacitor has also been realized by using WO₃ urchin-like nanostructures and a graphene paper electrode, revealing the highest energy density (90 W × h/kg) at a power density of 90 W × kg⁻¹ and the highest power density (9000 W/kg) at an energy density of 18 W × h/kg. The presented correlation among physical features and electrochemical performances of WO₃ nanostructures provides a solid base for further developing energy storage devices based on transition metal oxides. Full article

Tungsten trioxide/graphene oxide (WO₃/GO) nanocomposites have been successfully synthesized using in situ and ex situ chemical approaches. Graphite and tungsten carbide (WC) were employed to perform in situ synthesis, and WO₃ and GO were employed to perform the ex situ synthesis of WO₃/GO nanocomposites. GO, which was required for ex situ synthesis, is synthesized via the modified and improved Hummers method. XRD, SEM/EDS, and FTIR are used for the characterization of the nanocomposite. From the XRD of the WO₃/GO nanocomposites, it was observed that WO₃ distributed uniformly on graphene oxide sheets or was incorporated between the sheets. The photocatalytic activities of WO₃/GO nanocomposites were evaluated by methylene blue (MB) adsorption and visible light photocatalytic degradation activities by UV-vis spectroscopy. The results showed that the efficiency of the photocatalytic activity of the nanocomposite depends on different synthesis methods and the morphology resulting from the changed method. WO₃/GO nanocomposites synthesized by both methods exhibited much higher photocatalytic efficiencies than pure WO₃, and the best degradation efficiencies for MB was 96.30% for the WO₃/GO in situ synthesis nanocomposite. Full article