Search Results (149)

We reported a simplified one-step emulsification strategy to prepare bi-continuous emulsions with a gel-like property using the pH-responsive self-assembled aggregates of an amphiphilic random copolymer poly (styrene-co-methacrylic acid) (P(St-co-MAA)) as the interfacial stabilizers. Using caprylic/capric triglyceride (GTCC) as the oil phase, 1.0% P(St-co-MAA) aqueous solution with a pH between 7.0 and 8.0 as the water phase, and an oil/water phase ratio of 6:4, bi-continuous emulsions could be formed directly through one-step emulsification. Systematic characterization with a fluorescence microscope, scanning electron microscope, and confocal laser scanning microscope confirmed the formation of the bi-continuous emulsions. The three-phase contact angle measurements confirmed that the surface wettability of the self-assembled aggregates changed with pH, and the three-phase contact angles of the bi-continuous emulsions formed at a pH between 7.0 and 8.0 were close to 90°. Furthermore, rheological analysis of the bi-continuous emulsion showed the storage modulus (G′) dominating over the loss modulus (G″), which verified that the bi-continuous emulsion was attributed to the existence of a three-dimensional elastic gel network. The pH-dependent wettability of the self-assembled aggregates as the stabilizers enabled pH to control the emulsion type from O/W to bi-continuous to W/O. The work provides a simple, rapid, and robust approach to preparing bi-continuous emulsions without intricate particle modifications and cumbersome procedures. Full article

Developing green water disinfection technology has been attracting much attention all over the world. In this work, a WO₃/BiOBr@Si composite was obtained through the solvothermal process, which exhibited denser and fuller intersecting petal-like spheres (1–3 μm in diameter) and retained its 3D sheet-like pore structure. The optical and electrochemical analysis demonstrated that the doped Si showed insignificant improvement in UV-Vis light absorption but greatly promoted the electron-hole separation efficiency and charge transfer capability on the surface of the catalyst at a 4.6 wt% Si doping dosage, resulting in an excellent performance in the inactivation of Escherichia coli (E. coli) under the irradiation of visible light. Under the optimal conditions (0.5 g/L of WO₃/BiOBr@Si dosage, 10⁷ CFU mL⁻¹ of E. coli concertation, and 30 min of treating time), the largest log value decline (6.6) occurred with WO₃/BiOBr@1.0Si, which was 3.3 and 1.8 times larger than those of BiOBr (2.0) and WO₃/BiOBr (3.7). According to the TEM, SEM, EDS, XRD, FTIR, and XPS analyses, in the photocatalytic system, the hole (h⁺) and •OH were the main species for inactivating E. coli cells. These oxidizing species could attack the components on the surface of cells (such as the hydroxyl, carbonyl, ester, and amide groups of polysaccharides (PS) and proteins (PT)), resulting in the inactivation and destruction of the cell membranes and leakage of intracellular substances. The findings will provide a significant guide for developing an efficient catalyst for the green water disinfection process. Full article

Listeria monocytogenes (LM) contamination constitutes a paramount global threat to food safety, necessitating the urgent development of advanced, rapid, and non-destructive detection methodologies to ensure food security. This study successfully synthesized Bi₂WO₆ nanoflowers through optimized feed ratios of raw materials and further functionalized them with noble metal Au to construct a high-performance Au-Bi₂WO₆ composite nanomaterial. The composite exhibited high sensing performance toward acetoin, including high sensitivity (R_a/R_g = 36.9@50 ppm), rapid response–recovery kinetics (13/12 s), and excellent selectivity. Through UV-Vis diffuse reflectance spectroscopy (UV-Vis DRS) and X-ray photoelectron spectroscopy (XPS) characterizations, efficient electron exchange between Au and Bi₂WO₆ was confirmed. This electron exchange increased the initial resistance of the material, effectively enhancing the response value toward the target gas. Furthermore, the chemical sensitization effect of Au significantly increased the surface-active oxygen content, promoted gas–solid interfacial reactions, and improved the adsorption capacity for target gases. Compared to conventional turbidimetry, the Au-Bi₂WO₆ nanoflower-based gas sensor demonstrates superior practical potential, offering a novel technological approach for non-destructive and rapid detection of foodborne pathogens. Full article

This study evaluates lead-free high-density polyethylene (HDPE) composites reinforced with high-Z oxides (Bi₂O₃, WO₃, Gd₂O₃, TeO₂, and a Bi₂O₃/WO₃ hybrid) as lightweight materials for gamma-ray and fast-neutron shielding. A hybrid computational framework combining Phy-X/PSD with Geant4 Monte Carlo simulations was used to obtain key shielding parameters, including the linear and mass attenuation coefficients (μ, μ/ρ), half-value layer (HVL), mean free path (MFP), effective atomic number (Z_eff), effective electron density (N_eff), exposure and energy-absorption buildup factors (EBF, EABF), and fast-neutron removal cross section (Σ_R). The incorporation of heavy oxides produced a pronounced improvement in gamma-ray attenuation, particularly at low energies, where the linear attenuation coefficient increased from below 1 cm⁻¹ for neat HDPE to values exceeding 130–150 cm⁻¹ for Bi- and W-rich composites. In the intermediate Compton-scattering region (≈0.3–1 MeV), all oxide-reinforced systems maintained a clear attenuation advantage, with μ values around 0.12–0.13 cm⁻¹ compared with ≈0.07 cm⁻¹ for pure HDPE. At higher photon energies, the dense composites continued to outperform the polymer matrix, yielding μ values of approximately 0.07–0.09 cm⁻¹ versus ≈0.02 cm⁻¹ for HDPE due to enhanced pair-production interactions. The Bi₂O₃/WO₃ hybrid composite exhibited attenuation behavior comparable, and in some regions slightly exceeding, that of the single-oxide systems, indicating that mixed fillers can effectively balance density and shielding efficiency. Oxide addition significantly reduced exposure and energy-absorption buildup factors below 1 MeV, with a moderate increase at higher energies associated with secondary radiation processes. Fast-neutron removal cross sections were also modestly enhanced, with Gd₂O₃-containing composites showing the highest values due to the combined effects of hydrogen moderation and neutron capture. The close agreement between Phy-X/PSD and Geant4 results confirms the reliability of the dual-method approach. Overall, HDPE composites containing about 60 wt.% oxide filler offer a practical compromise between shielding performance, manufacturability, and environmental safety, making them promising candidates for medical, nuclear, and aerospace radiation-protection applications. Full article

Environmentally friendly materials with superior structural, physical, optical, and shielding capabilities are of great technological importance and are continually being investigated. In this work, novel multicomponent borate glasses with the composition xTiO₂-10BaO-5Al₂O₃-5WO₃-20Bi₂O₃-(60-x) B₂O₃, where 0 ≤ x ≤ 15 mol%, were produced via the melt-quenching technique. The increase in TiO₂ content results in a decrease in molar volume and a corresponding increase in density, indicating the formation of a compact, rigid, and mechanically hard glass network. Elastic constant measurements further confirmed this behavior. FTIR analysis confirms the transformation of BO₃ to BO₄ units, signifying improved network polymerization and structural stability. The prepared glasses exhibit an optical absorption edge in the visible region, demonstrating their strong ultraviolet light blocking capability. Incorporation of TiO₂ leads to an increase in refractive index, optical basicity, and polarizability, and a decrease in the optical band gap and metallization number; all of these suggest enhanced electron density and polarizability of the glass matrix. Radiation shielding properties were evaluated using Phy-X/PSD software. The outcomes illustrate that the Mass Attenuation Coefficient (MAC), Effective Atomic Number (Z_eff), Linear Attenuation Coefficient (LAC) increase, while Mean Free Path (MFP) and Half Value Layer (HVL) decrease with increasing TiO₂ at the expense of B₂O₃, confirming superior gamma-ray attenuation capability. Additionally, both TiO₂-doped and undoped samples show higher fast neutron removal cross sections (FNRCS) compared to several commercial glasses and concrete materials. Overall, the incorporation of TiO₂ significantly enhances the optical performance and radiation-shielding efficiency of the environmentally friendly glass system, making these potential candidates for advanced photonic devices and radiation-shielding applications. Full article

The photocatalytic activity of Bi₂WO₆ Aurivillius phase has been widely exploited for the degradation of a wide range of gaseous and aqueous molecules, as well as microorganisms, under the influence of visible irradiation. Strategies for the development of doped and co-doped bismuth tungstate materials require the thermodynamic data on this phase. The heat capacity of bismuth tungstate, Bi₂WO₆, was investigated using a DSC microcalorimeter on polycrystalline powder samples in the temperature range from 313 to 1103 K (40–830 °C) in two separate runs. The samples were synthesized by solid-state reaction from pure binary oxides at 1033 K (760 °C) in a platinum crucible with cover. The high temperature C_p(T) data were fitted by the Maier–Kelley equation and, from this relation, the standard molar heat capacity of γ-Bi₂WO₆ polymorph was estimated to be at 298.15 K 176.8 ± 3.9 J·K⁻¹·mol⁻¹. A reversible second-order transition of Bi₂WO₆ phase was observed in the experimental temperature range, with a peak close to 940 K (667 °C). Additionally, the extrapolation of C_p(T) to 0 K was proposed using a method based on the multiple Einstein model. Thermodynamic properties (heat capacity C_p(T), entropy S°(T), enthalpy H°(T), Gibbs energy G°(T)) of crystalline γ-Bi₂WO₆ were calculated in the temperature range of 298.15–1123 K (25–850 °C). Full article

CuWO₄ films were prepared on FTO glass substrates by the hydrothermal method. To improve their photocatalytic activity, the CuWO₄ films were further modified with BiOI using the successive ionic layer adsorption and reaction (SILAR) method. Characterization results indicate that BiOI and CuWO₄ achieved nanoscale mixing and formed a Type II p-n heterojunction. The heterojunction formation not only extends the light absorption threshold of CuWO₄ from 530 nm to 660 nm but also enhances the light absorption capacity across the entire solar spectrum. More importantly, the heterojunction formation facilitates the separation and transfer of photogenerated carriers and inhibits the recombination of photogenerated electrons and holes, which is evidenced by the results of PL spectra, photocurrent density, and EIS spectra. Compared with individual CuWO₄ films, the photocatalytic activity of BiOI/CuWO₄ heterojunction films in degrading the organic dye MB is increased by up to 1.17 times. Additionally, BiOI/CuWO₄ heterojunction films exhibit certain activity in the photocatalytic degradation of polystyrene (PS) nanoplastics and are capable of reducing the average particle size of nanoplastics from 425 nm to 325 nm within 80 h. Full article

Recently, the design and fabrication of novel electrode materials for electrochemical and electronic devices have received the widespread attention of the scientific community. In particular, electrochemical sensors and supercapacitors (SCs) involve the use of catalysts, which can enhance the electrochemical reactions at the surface of the electrode. Bismuth tungstate (Bi₂WO₆) is a cost-effective and efficient electrode material with decent optoelectronic properties and stability. The properties of Bi₂WO₆ can be improved by incorporating carbon-based materials, and the resulting composite may be a promising electrode material for electrochemical sensing and SCs. As per the available reports, Bi₂WO₆ has been combined with various nanostructured and conductive materials for electrochemical sensing and SC applications. This review discusses synthetic methods for the preparation of Bi₂WO₆. Progress in the construction of hybrid composites for electrochemical sensing and SC applications is reviewed. The Conclusion section discusses the role of electrode materials and their limitations with future perspectives for electrochemical sensing and SCs. It is believed that the present review may be useful for researchers working on Bi₂WO₆-based materials for electrochemical sensing and SC applications. Full article

The rational design of photoanode materials is pivotal for advancing photoelectrochemical (PEC) water splitting toward sustainable hydrogen production. This review highlights recent progress in the machine learning (ML)-assisted development of nanostructured metal oxide photoanodes, focusing on bridging materials discovery and device-level performance optimization. We first delineate the fundamental physicochemical criteria for efficient photoanodes, including suitable band alignment, visible-light absorption, charge carrier mobility, and electrochemical stability. Conventional strategies such as nanostructuring, elemental doping, and surface/interface engineering are critically evaluated. We then discuss the integration of ML techniques—ranging from high-throughput density functional theory (DFT)-based screening to experimental data-driven modeling—for accelerating the identification of promising oxides (e.g., BiVO₄, Fe₂O₃, WO₃) and optimizing key parameters such as dopant selection, morphology, and catalyst interfaces. Particular attention is given to surrogate modeling, Bayesian optimization, convolutional neural networks, and explainable AI approaches that enable closed-loop synthesis-experiment-ML frameworks. ML-assisted performance prediction and tandem device design are also addressed. Finally, current challenges in data standardization, model generalizability, and experimental validation are outlined, and future perspectives are proposed for integrating ML with automated platforms and physics-informed modeling to facilitate scalable PEC material development for clean energy applications. Full article

The current research introduces a cost-effective thermal coating process using a tinning surfacing technique to synthesize WO₃ nanoparticle-reinforced Sn-20Bi (S20B) alloy coating on low-carbon steel (LCS). A ball-milling machine was used for mechanical mixing and blending of Sn and Bi powders together with 0.25 wt.% WO₃ nanoparticles. The produced powders were mixed with a prefabricated flux in two different ratios to optimize the best surface coating morphology. The synthesized coatings were spread out on the surface of the LCS in a layer of 0.25 g cm⁻² and were heated for 3, 4, and 5 min at 370 °C. A series of corrosion tests was carried out to understand the effect of the different S20B and S20B-WO₃ coatings on the corrosion passivation of the LCS samples in 3.5% NaCl solution. The coating surface layer thickness increased by decreasing the percentage of flux in the synthesized coating. Increasing the heating time (from 3 min to 5 min) increases surface coating uniformity and slightly boosts the average Fe−Sn intermetallic (IMC) layer thickness (from 1.7 ± 0.3 µm to 3.3 ± 0.3 µm). By incorporating 0.25 wt.% WO₃ nanoparticles into the S20B coating surface layer, a uniform microstructure was achieved and the thickness of the Fe–Sn IMC layer was reduced to 2.6 ± 0.3 µm. This study found that the presence of WO₃ nanoparticles significantly improved the corrosion resistance of S20B-coated LCS. These results demonstrate that adding a small of WO₃ nanoparticles significantly enhances the microstructural integrity and corrosion resistance of S20B coatings on LCS. Full article

This study employs simulation tools to design and evaluate lightweight, lead-free polymer composites incorporating polytetrafluoroethylene (PTFE), polyethylene (PE), and polyetherimide (PEI) for gamma radiation shielding in nuclear medicine. Targeting clinically relevant photon energies from Tc-99m (140 keV), I-131 (364 keV), and Cs-137 (662 keV), composites’ structural and shielding performance with Bi₂O₃ and WO₃ was assessed using XCOM and Phy-X/PSD. PEI emerged as the most suitable polymer for load-bearing and thermally exposed applications, offering superior mechanical stability and dimensional integrity. Bi₂O₃-WO₃ fillers for Tc-99m achieved a ~7000-fold increase in MAC, I-131 ~2063-fold, and Cs-137 ~1370-fold compared to PbO₂. The PEI-75Bi₂O₃-25WO₃ achieved a ~21-fold reduction in half-value layer (HVL) compared to lead for Tc-99m. For higher-energy isotopes of I-131 and Cs-137, HVL reductions of ~0.44-fold and ~0.08-fold, respectively, were achieved. The results demonstrate that high-Z dual filler polymer composites have an equal or enhanced attenuation properties to lead-based shielding, whilst also enhancing the polymer composites’ mechanical and thermal characteristics. As the use of ionizing radiation increases, so does the potential risks; high-Z dual filler polymer composites provide a sustainable, lightweight, non-toxic alternative to conventional lead shielding. Full article

Tetracycline hydrochloride pollution poses a serious environmental threat; however, it is difficult to deal with by conventional methods. In this study, the Z-scheme BiOCl/Bi₂WO₆ composite was hydrothermally synthesized and evaluated for its ability to decompose tetracycline hydrochloride under visible light. The composite material was systematically characterized by XRD, SEM, TEM/HRTEM, XPS, FTIR, BET, PL, UV-Vis DRS, and EPR to analyze its structure, morphology, and optical/electrochemical properties. Characterization revealed that the composite featured a flower-ball structure with broader light absorption and higher solar energy efficiency. A narrow bandgap further facilitated charge separation, boosting photocatalytic performance. Among the synthesized materials, the 20% BiOCl/Bi₂WO₆ composite exhibited the best performance, removing 94% of tetracycline hydrochloride in 60 min, which was 5.2 times and 1.4 times higher than pure BiOCl and Bi₂WO₆, respectively. The rate constant was 10.8 times and 2.5 times higher than that of pure BiOCl and Bi₂WO₆. After five cycles, it maintained the 88.7% removal rate, with X-ray diffraction analysis confirming its structural stability and well mechanical properties. Electron paramagnetic resonance and radical scavenging experiments identified photogenerated holes (h⁺) and superoxide radicals (·O₂⁻) as the primary active species. This work highlights the fact that the prepared Z-scheme BiOCl/Bi₂WO₆ composite exhibited excellent photocatalytic performance in the degradation of tetracycline hydrochloride, demonstrating promising potential for practical applications. Full article

Hydrogen and oxygen serve as energy carriers that can ease the transition of energy due to their high energy densities. Nonetheless, their production processes entail the development of efficient and low-cost storage and conversion technologies. In this regard, photoelectrocatalysts are materials based on the photoelectronic effect where electrons and holes interact with H₂O, producing H₂ and O_2, and in some cases, this is achieved with acceptable efficiency. Although there are several reviews on this topic, most of them focus on traditional semiconductors, such as TiO₂ and ZnO, neglecting others, such as those based on non-noble metals and organic ones. Herein, semiconductors like CdSe, NiWO₄, Fe₂O₃, and others have been investigated and compared in terms of photocurrent density, band gap, and charge transfer resistance. In addition, this brief review aims to discuss the mechanisms of overall water-splitting reactions from a photonic point of view and subsequently discusses the engineering of material synthesis. Advanced composites are also addressed, such as WO₃/BiVO₄/Cu₂O and CN-FeNiOOH-CoOOH, which demonstrate high efficiency by delivering photocurrent densities of 5 mAcm⁻² and 3.5 mA cm⁻² at 1.23 vs. RHE, respectively. Finally, the authors offer their perspectives and list the main challenges based on their experience in developing semiconductor-based materials applied in several fields. In this manner, this brief review provides the main advances in these topics, used as references for new directions in designing active materials for photoelectrocatalytic water splitting. Full article

The urgent need for sustainable CO₂ conversion technologies has driven the development of advanced photocatalysts that harness solar energy. This study employs a CTAB-assisted solvothermal method to fabricate a Z-scheme heterojunction Fe-MOFs/V_O-Bi₂WO₆ (FM/V_O-BWO) for photocatalytic CO₂ reduction. Positron annihilation lifetime spectroscopy (PALS) was employed to confirm the existence of oxygen vacancies, while spherical aberration-corrected transmission electron microscope (STEM) characterization verified the successful construction of heterointerfaces. X-ray absorption fine structure (XAFS) spectra confirmed that the defect configuration and heterostructure changed the surface chemical valence state. The optimized 1.0FM/V_O-BWO composite demonstrated exceptional photocatalytic performance, achieving CO and CH₄ yields of 60.48 and 4.3 μmol/g, respectively, under visible-light 11.8- and 1.5-fold enhancements over pristine Bi₂WO₆. The enhanced performance is attributed to oxygen vacancy-induced active sites facilitating CO₂ adsorption/activation. In situ molecular spectroscopy confirmed the formation of critical CO₂-derived intermediates (COOH* and CHO*) through surface interactions involving four-coordinated and two-coordinated hydrogen-bonded water molecules. Furthermore, the accelerated interfacial charge transfer efficiency mediated by the Z-scheme heterojunction has been conclusively demonstrated. This work establishes a paradigm for defect-mediated heterojunction design, offering a sustainable route for solar fuel production. Full article

This review analyzes TiO₂-based coatings formed by the plasma electrolytic oxidation (PEO) process of titanium for the photocatalytic degradation of methyl orange (MO) under simulated solar irradiation conditions. PEO is recognized as a useful technique for creating oxide coatings on various metals, particularly titanium, to assist in the degradation of organic pollutants. TiO₂-based photocatalysts in the form of coatings are more practical than TiO₂-based photocatalysts in the form of powder because the photocatalyst does not need to be recycled and reused after wastewater degradation treatment, which is an expensive and time-consuming process. In addition, the main advantage of PEO in the synthesis of TiO₂-based photocatalysts is its short processing time (a few minutes), as it excludes the annealing step needed to convert the amorphous TiO₂ into a crystalline phase, a prerequisite for a possible photocatalytic application. Pure TiO₂ coatings formed by PEO have a low photocatalytic efficiency in the degradation of MO, which is due to the rapid recombination of the photo-generated electron/hole pairs. In this review, recent advances in the sensitization of TiO₂ with narrow band gap semiconductors (WO₃, SnO₂, CdS, Sb₂O₃, Bi₂O₃, and Al₂TiO₅), doping with rare earth ions (example Eu³⁺) and transition metals (Mn, Ni, Co, Fe) are summarized as an effective strategy to reduce the recombination of photo-generated electron/hole pairs and to improve the photocatalytic efficiency of TiO₂ coatings. Full article