Tungsten Trioxide Nanoparticles Research Articles

Synthesis and characterization of WO3-GO nanocomposite for hydrogen storage, electrochemical, antibacterial and anticancer applications

Tungsten trioxide nanoparticles (WO3 NPs), Graphene oxide nanosheets (GO NSs), and WO3-GO (50 mg and 100 mg) nanocomposites (NCs) were successfully synthesized by using precipitation, modified Hummer's and ultrasonication methods, respectively. Various characterization techniques were used to confirm the formation of individual and composite materials. Hydrogen storage, electrochemical, antibacterial and anticancer properties of the synthesized materials were studied. Formation of the composite was confirmed by XRD, Raman and XPS analyses. Surface area and pore size distribution of WO3 NPs and WO3-GO NC were studied by using BET analysis. Hydrogen storage capacity of WO3-GO 50 mg and WO3-GO100 mg NCs was found to be 1.05 and 2.08 wt%, respectively. XRD, Raman, elemental and TG analyses were used to examine the adsorption and desorption of hydrogen. WO3-GO NCs showed higher specific capacitance as compared to WO3 NPs. Antibacterial activity against E. coli, S. aureus bacteria and anticancer effect against human breast cancer cells of WO3 NPs and WO3-GO NC were examined. Based on the studies, it is evident that the inclusion of GO enhanced the hydrogen storage, specific capacitance, antibacterial and anticancer activities of the composite.

Advancing gamma radiation shielding with Bitumen-WO₃ composite materials

This research focuses on a manner in which bitumen-WO₃ (petroleum-derived bitumen mixed with tungsten trioxide nanoparticles) materials can be a good shielding candidate against gamma radiation. The objective we set in mixing WO₃ nanoparticles with bitumen was to take advantage of both the bitumen's natural qualities and the WO₃'s excellent shielding capabilities. The prepared composites were tested against various gamma-ray energies emitted from multiple gamma-ray sources to examine their shielding capabilities. The X-ray diffraction (XRD) analysis of the composites' structural properties verified the effective integration of the WO₃ with the bitumen structure. Scanning electron microscopy (SEM) showed that microstructural changes, such as an increase in material density and an improvement in particle dispersion, are caused by a rise in WO3 concentration, which is an essential step toward efficient shielding. Then, the Mean Free Path (MFP), Half-value Layer (HVL), and Linear Attenuation Coefficients (μl) were computed, showing that the composite's capacity to reduce gamma radiation is much enhanced by raising the WO₃ content, especially at lower gamma-ray energies. For instance, at 20 keV, the LAC of 50 wt% WO₃-bitumen composite increased to 9.18 cm⁻1 compared to pure bitumen's 0.40 cm⁻1, while the HVL decreased from 1.73 cm to 0.08 cm, and the MFP dropped from 2.3 cm to 0.1 cm” The results demonstrate the potential of bitumen-WO₃ composites as a sustainable and efficient material for radiation shielding, particularly highlighting their applicability in various sectors, including the development of building wall paints against gamma radiation.

Reversibly photochromic wood constructed by electric field-assisted self-assembled chitosan and tungsten trioxide coatings

ABSTRACT The photochromic properties are highly desirable for advanced wood applications, but they have not been extensively studied. To incorporate photochromic capabilities into wood materials, composite coatings were developed on the wood surface using an electric field-assisted layer-by-layer (LBL) self-assembly technique. The composite coatings consist of cationic chitosan and anionic tungsten trioxide (WO3) nanoparticles. By applying a direct current voltage during the deposition process, a well-organized distribution of WO3 nanoparticles was achieved, resulting in a uniform coverage of the wood substrate. This assembly process facilitated the creation of structured photochromic coatings with minimal nanoparticle fillers, a straightforward and rapid procedure, and potential for large-scale production. Lab colorimetric results demonstrated that the wooden substrate changed color from its natural state to blue when exposed to UV light. UV-vis spectroscopy further confirmed the efficient absorption of WO3 and photochromic properties of the modified wood.

Dielectric and structural properties of polyaniline-tungsten trioxide nanocomposites: For the packing of nano-electronic devices and EMI shielding

Polymer nanocomposites (PNCs) have showed the significant applications in the fields of packing, energy, safety, defense, sensors, EMI shielding, optoelectronics etc. Tungsten trioxide nanoparticles (NPs) were prepared by propellant chemistry technique using Azadirachta indica extracts as a fuel/surfactant. Conducting polyaniline (PANI) was prepared using aniline monomer and suitable polymerizing agents. Ex-situ nanocomposites were prepared by mixing the different weight percentage of NPs into PANI matrix. For the better dispersion of NPs in to the matrix, solvents like Dodesyl benzene sulphonic acid (DBSA) and Camphor sulphonic acid (CSA) were used. Crystal structure, morphological features and their dielectric response at room temperature were reported. Electromagnetic Shielding (EMI) studies were compared between the PANI-WO3 composites prepared by CSA and DBSA solvents. Composites showed worthy shielding response of 80 dB with CSA and 38 dB with DBSA. Here, the protonation of the solvent and the dispersion of NPs with the polymer matrix matters for the shielding efficiency. Hence, prepared materials are suitable for packing of electronic devices which provides the better EMI shielding and also suppress the heat through effective absorption of EM waves of X-Band.

Combining WO3@AuNPs with Poly(amidoamine) Allows Sensitive Electrochemical Detection of DR1 Based on Dual Signal Amplification.

Down-regulator of transcription 1 (DR1) is considered as a biomarker of hashimoto's thyroiditis (HT), which is a risk factor for thyroid cancer. Here, a label-free electrochemical biosensor for DR1 detection was constructed based on polyamidoamine (PAMAM) polymer and the nanocomposite (WO3@AuNPs) composed of tungsten trioxide (WO3) and gold nanoparticles (AuNPs). WO3@AuNPs was obtained by combining monolayer WO3 nanosheets, which has high conductivity, and AuNPs. The modification of WO3@AuNPs can not only increase the conductivity of the electrode but also provide more active sites for signaling units, thus greatly improve the sensitivity of the sensor. The polymer PAMAM is biocompatible and non-immunogenic, and its end functional group can bind to the target molecules, providing them with more binding sites and thus improving the sensitivity of the sensor. Under optimal conditions, the label-free biosensor showed a good linear relationship between the logarithm of DR1 concentration and the impedance in the range of 10 fg ⋅ mL-1 to 100 ng ⋅ mL-1, with a detection limit as low as 0.3 fg ⋅ mL-1. Besides, this label-free electrochemical platform exhibited satisfactory selectivity and anti-interference capability in human serum samples. Therefore, this method has considerable potential in clinical detection of DR1.

Preparation, structural characterization, optical, photoluminescence, AC electrical conductivity and broadband dielectric properties of WO3 reinforced PEG/CS blend for futuristic optoelectronic and energy storage devices

Polymer nanocomposites (PNCs) composed of biopolymers and metallic oxides are important classes of materials. In addition to the environmental and economic considerations, these materials became the best candidates for various industrial fields. In the current study, solution cast procedure is used to prepare polymer nanocomposites (PNCs) based on polyethylene glycol (PEG)/chitosan (CS) blend and varying concentrations of tungsten trioxide nanoparticles (WO3 NPs), as a nanofiller. TEM micrograph shows that WO3 NPs have particle sizes of 5–32 nm their shapes are cubic and spherical. The XRD results reveal the semicrystalline of PEG/CS blend through showing three distinct diffraction peaks at 2θ = 7.42°, 19.47° and 23.62° and the degree of crystallinity is decreased after the incorporation of WO3 NPs due to the formation of polymer-nanoparticle interactions as indicated by FTIR spectra. The values of optical energy bandgap (direct and indirect) reduce while the Urbach energy increases with raising the concentration of WO3 NPs in the PEG/CS matrix. The PEG/CS-WO3 films' PL spectra show a photoemission peak at about 387 nm, where this peak loses intensity and becomes broader due to the induced defects and increase of disordering within the nanocomposite films. Additionally, the results of the dielectric investigation show an increase in the dielectric constant, dielectric loss, and AC electrical conductivity, which may be a sign of an increase of charge carriers and the content of amorphous regions that assists the movement of charge carriers. The DC electrical conductivity and conduction mechanism are also reported. Argand plot shows a half semicircle implying the Debye-type relaxation mechanism. The experimental results suggest the use of PEG/CS-WO3 nanocomposites as a possible contender for futuristic energy storage and optoelectronic applications.

Reinforced PS-PVDF-WO3 superhydrophobic antiwetting membrane for membrane distillation

Membrane distillation (MD) is an energy-efficient desalination process with abilities to achieve nearly zero liquid discharge and recovery of resources. Nevertheless, MD's transition from laboratory to industrial scale has been largely challenged by expensive and complex fabrication methods for hydrophobic membranes, as well as lack of resistance against wetting and scaling. Present study demonstrates about the development of a hydrophobic electrospun membrane using a low-cost polystyrene (~1.057 $ per kg) polymer blended with PVDF (~80 $ per kg), followed by the surface modification via electrospraying of silane functionalized tungsten trioxide (WO3) nanoparticles. The characteristics of the fabricated membrane in terms of deionized water contact angle revealed ultra-high surface contact angle (~172°) and low sliding angle (<5°). The low thermal conductivity (~0.166 W/mK) of electrospun membrane accredited decreases in temperature polarization during MD operation, resulting in enhanced transportation of water vapors from feed to permeate side. Furthermore, the electrospun membrane attained resilience against wetting, along with stable permeate flux (~25 LMH) and high salt rejection (>99.9 %) with low surface tension (~28 mN/m) saline feed. Tensile tests (firm up to 45 N) and harsh chemical exposure (durable at pH 2 and pH 12) confirmed the structural robustness of the fabricated membrane.

Research on pH Sensor Based on Cuprous Oxide Film Modified with Tungsten Trioxide Nanoparticles

Research on pH Sensor Based on Cuprous Oxide Film Modified with Tungsten Trioxide Nanoparticles

Structure, Optics, Visible Light and Photocatalytic Activity of Pure and Pd Doped Tungsten Trioxide Nanoparticles Synthetized by the Microwave Irradiation Method

Structure, Optics, Visible Light and Photocatalytic Activity of Pure and Pd Doped Tungsten Trioxide Nanoparticles Synthetized by the Microwave Irradiation Method

Deep eutectic solvent assisted hydrothermal synthesis of photochromic and nontoxic tungsten oxide nanoparticles

In this work, hydrothermal methods and deep eutectic solvents were combined for the first time to prepare tungsten trioxide nanoparticles in an easy and green manner improving their optical and photochromic properties.

Preparation of high-strength photochromic alginate fibers based on the study of flame-retardant properties

Color-changing fibers have attracted much attention for their wide applications in camouflage, security warnings, and anti-counterfeiting. The inorganic color-changing material tungsten trioxide (WO3) has been widely investigated for its good stability, controllability, and ease of synthesis. In this study, photochromic alginate fibers (WO3@Ca-Alg) were prepared by incorporating UV-responsive hybrid tungsten trioxide nanoparticles in the fiber production process. The prepared photochromic alginate fibers changed from white to dark blue after 30 min of UV irradiation and returned to their original color after 64 h. It can be seen that WO3@Ca-Alg has the advantage of long color duration. The strength of this fiber reached 2.61 cN/dtex and the limiting oxygen index (LOI) was 40.9 %, which indicates that the fiber exhibited mechanical resistance and flame-retardant properties. After the cross-linking of WO3@Ca-Alg by sodium tetraborate, a new core-shell structure was generated, which was able to encapsulate tungsten trioxide in it, thus reducing the amount of tungsten trioxide loss, and its salt and washing resistance was greatly improved. This photochromic alginate fiber can be mass produced and spun into yarn.

Scalable Photochromic Film for Solar Heat and Daylight Management.

The adaptive control of sunlight through photochromic smart windows could have a huge impact on the energy efficiency and daylight comfort in buildings. However, the fabrication of inorganic nanoparticle and polymer composite photochromic films with a high contrast ratio and high transparency/low haze remains a challenge. Here, a solution method is presented for the in situ growth of copper-doped tungsten trioxide nanoparticles in polymethyl methacrylate, which allows a low-cost preparation of photochromic films with a high luminoustransparency (luminous transmittance Tlum = 91%) and scalability (30 × 350 cm2 ). High modulation of visible light (ΔTlum = 73%) and solar heat (modulation of solar transmittance ΔTsol = 73%, modulation of solar heat gain coefficient ΔSHGC = 0.5) of the film improves the indoor daylight comfort and energy efficiency. Simulation results show that low-e windows with the photochromic film applied can greatly enhance the energy efficiency and daylight comfort. This photochromic film presents an attractive strategy for achieving more energy-efficient buildings and carbon neutrality to combat global climate change.

Fabrication and Characterization of a Poly(3,4-ethylenedioxythiophene)@Tungsten Trioxide-Graphene Oxide Hybrid Electrode Nanocomposite for Supercapacitor Applications.

With the rapid development of nanotechnology, the study of nanocomposites as electrode materials has significantly enhanced the scope of research towards energy storage applications. Exploring electrode materials with superior electrochemical properties is still a challenge for high-performance supercapacitors. In the present research article, we prepared a novel nanocomposite of tungsten trioxide nanoparticles grown over supported graphene oxide sheets and embedded with a poly(3,4-ethylenedioxythiophene) matrix to maximize its electrical double layer capacitance. The extensive characterization shows that the poly(3,4-ethylenedioxythiophene) matrix was homogeneously dispersed throughout the surface of the tungsten trioxide-graphene oxide. The poly(3,4-ethylenedioxythiophene)@tungsten trioxide-graphene oxide exhibits a higher specific capacitance of 478.3 F·g-1 at 10 mV·s-1 as compared to tungsten trioxide-graphene oxide (345.3 F·g-1). The retention capacity of 92.1% up to 5000 cycles at 0.1 A·g-1 shows that this ternary nanocomposite electrode also exhibits good cycling stability. The poly(3,4-ethylenedioxythiophene)@tungsten trioxide-graphene oxide energy density and power densities are observed to be 54.2 Wh·kg-1 and 971 W·kg-1. The poly(3,4-ethylenedioxythiophene)@tungsten trioxide-graphene oxide has been shown to be a superior anode material in supercapacitors because of the synergistic interaction of the poly(3,4-ethylenedioxythiophene) matrix and the tungsten trioxide-graphene oxide surface. These advantages reveal that the poly(3,4-ethylenedioxythiophene)@tungsten trioxide-graphene oxide electrode can be a promising electroactive material for supercapacitor applications.

Plasma synthesis of various polymorphs of tungsten trioxide nanoparticles using gliding electric discharge in humid air: characterization and photocatalytic properties

A gliding electric arc (glidarc) discharge generates a low-temperature plasma at atmospheric pressure. When the discharge occurs in humid air as the feed gas, the chemistry of a glidarc plasma consists of in situ formation of HO° and NO° as the primary chemical species. Tungsten trioxide (WO3) nanoparticles were successfully prepared by exposure of a liquid precursor to glidarc plasma. The WO3 samples were calcined at three different temperatures (300 °C, 500 °C and 800 °C), resulting in different pure polymorphs: γ-WO3 (at 300 °C), β-WO3 (at 500 °C) and α-WO3 (at 800 °C) according to x-ray diffraction analysis. The identification of WO3 compounds was also confirmed by attenuated total reflection Fourier transform infrared spectroscopy analysis. Increase in the calcination temperature of WO3 induced a decrease in its specific surface area according to Brunauer–Emmett–Teller nitrogen physisorption analysis. The UV-visible results showed that the absorption bands of plasma-WO3 samples were more intense than those of WO3 samples obtained by a precipitation route, a classical method used for comparison. Consequently, this parameter can improve the photocatalytic properties of WO3 under visible light. The photodegradation (in sunlight conditions) of gentian violet, chosen as a model pollutant, confirmed the photocatalytic properties of plasma-WO3 samples. This novel synthesis method has great potential to improve the efficiency of advanced tungsten trioxide-based functional material preparation, as well as in pollution-reducing and energy-saving tungsten extractive metallurgy.

Improving the optical, photoluminescence, and electrical properties of PEO/NaAlg-WO3 nanocomposites for optoelectronic and nanodielectric applications

Nanocomposites based on polyethylene oxide (PEO)/Sodium Alginate (NaAlg) with varying content of tungsten trioxide nanoparticles (WO3 NPs) have been synthesized by using a green solvent casting method. Through the use of X-ray diffraction (XRD), Fourier transforms infrared (FTIR), and Ultraviolet–visible spectroscopy (UV–Vis.), the interaction of mixed components has been evaluated. Studies using spectroscopy have shown that WO3 nanoparticles and the blend's component parts interact strongly at their interfaces. XRD confirms the increasing amorphous propensity of the PEO/NaAlg film with increasing nanofiller loading. FTIR implies the development of molecular complex of the polymer with the nanofiller. From UV–Vis analysis, Tauc's relation was used to specify the direct and indirect bandgap energy. The Eg (direct) of pure PEO/NaAlg was considerably decreased from 4.23 to 3.04 eV by adding 2.0 wt% of WO3 NPs. The fluorescence for various WO3 NPs concentrations in PEO/NaAlg blend films was analyzed. The PEO/NaAlg blend's fluorescence intensity decreased with increased doped with WO3 NPs. The films made of nanocomposites also had their dielectric behavior and electrical conductivity examined. In contrast to the electrical conductivity (AC), the dielectric constant and dielectric loss of PEO/NaAlg-WO3 nanocomposites drop as the frequency of the electric field rises. The investigation revealed that an increase in WO3 concentration led to a corresponding rise in the nanocomposites' dielectric loss and dielectric constant values. The fabricated system of PEO/NaAlg-WO3 NPs nanocomposites films showing improved in AC conductivity and dielectric characteristics and could be suggested in optoelectronic and nanodielectric devices.

Point-of-care diagnostics for rapid determination of prostate cancer biomarker sarcosine: application of disposable potentiometric sensor based on oxide-conductive polymer nanocomposite

One of the most important reasons for an increased mortality rate of cancer is late diagnosis. Point-of-care (POC) diagnostic sensors can provide rapid and cost-effective diagnosis and monitoring of cancer biomarkers. Portable, disposable, and sensitive sarcosine solid-contact ion-selective potentiometric sensors (SC-ISEs) were fabricated as POC analyzers for the rapid determination of the prostate cancer biomarker sarcosine. Tungsten trioxide nanoparticles (WO3 NPs), polyaniline nanoparticles (PANI NPs), and PANI-WO3 nanocomposite were used as ion-to-electron transducers on screen-printed sensors. WO3 NPs and PANI-WO3 nanocomposite have not been investigated before as ion-to-electron transducer layers in potentiometric SC sensors. The designated sensors were characterized using SEM, XRD, FTIR, UV-VIS spectroscopy, and EIS. The inclusion of WO3 and PANI in SC sensors enhanced the transduction at the interface between the screen-printed SC and the ion-selective membrane, offering lower potential drift, a longer lifetime, shorter response time, and better sensitivity. The proposed sarcosine sensors exhibited Nernstian slopes over linear response ranges 10−3–10−7 M, 10−3–10−8 M, 10−5–10−9 M, and 10−7–10−12 M for control, WO3 NPs, PANI NPs, and PANI-WO3 nanocomposite-based sensors, respectively. From a comparative point of view between the four sensors, PANI-WO3 nanocomposite inclusion offered the lowest potential drift (0.5 mV h−1), the longest lifetime (4 months), and the best LOD (9.95 × 10−13 M). The proposed sensors were successfully applied to determine sarcosine as a potential prostate cancer biomarker in urine without prior sample treatment steps. The WHO ASSURED criteria for point-of-care diagnostics are met by the proposed sensors.Graphical abstract

Remediation of recalcitrant pollutants in water solution using visible light responsive cerium-doped tungsten trioxide nanoparticles.

In order to attain a solar energy-driven photocatalyst for wastewater remediation, cerium-doped WO3 (W1-xCexO3 with x = 0, 0.02, 0.04, 0.06, and 0.08) nanoparticles have been synthesized via a chemical co-precipitation technique. X-ray diffraction (XRD) analysis confirmed that W1-xCexO3 nanoparticles retained their monoclinic structure even after doping. The presence of the vast number of defects produced in the WO3 lattice was corroborated by Raman spectroscopy. Scanning electron microscopy confirmed the spherical shape of the nanoparticles with particle size range 50-76 nm. The optical band gap of W1-xCexO3 nanoparticles decreases from 3.07 to 2.36 eV with an increase in x, as confirmed by UV-Vis spectroscopy. Photoluminescence (PL) spectroscopy confirmed that the minimum rate of recombination was observed for W1-xCexO3 with x = 0.04. Degradation efficiency was explored for methyl violet (MV) and rhodamine-B (Rh-B) with 0.01 g of photocatalyst in a photoreactor chamber having a 200-W xenon lamp as a visible source of light. The results showed that the maximum photo-decolorization towards MV (94%) and rhodamine-B (79.4%) was observed in x = 0.04 sample in just 90 min because of its least recombination rate, highest adsorption capacity, and optimum band edge positions. Intriguingly, it has been observed that the modification with cerium in WO3 nanoparticles enhances the photocatalytic activity by narrowing the band gap and by efficaciously lowering the recombination rate due to electron entrapment by defects produced in the lattice.

Optical, Thermal, and Electrical Characterization of Polyvinyl Pyrrolidone/Carboxymethyl Cellulose Blend Scattered by Tungsten-Trioxide Nanoparticles

The polymeric material polyvinyl pyrrolidine/carboxymethyl cellulose (PVP/CMC) was mixed with different quantities of tungsten-trioxide nanoparticles (WO3 NPs). The samples were created using the casting method and Pulsed Laser Ablation (PLA). The manufactured samples were analyzed by utilizing various methods. The halo peak of the PVP/CMC was located at 19.65°, confirming its semi-crystalline nature, as shown in the XRD analysis. FT-IR spectra of pure PVP/CMC composite and PVP/CMC composite incorporated with various contents of WO3 obtained a shift in band locations and change in intensity. Optical band gap was calculated via UV-Vis spectra, which decreased when increasing the laser-ablation time. Thermogravimetric analyses (TGA) curves showed that samples' thermal stability had improved. The frequency-dependent composite films were used to determine AC conductivity of the generated films. When increasing the content of tungsten-trioxide nanoparticles, both (ε') and (ε'') increased. The incorporation of tungsten trioxide enhanced the ionic conductivity of PVP/CMC/WO3 nano-composite to a maximum of 10-8 S/c. It is expected that these studies will have a significant impact on several utilizations, such as energy storage, polymer organic semiconductors, and polymer solar cells.

Enhanced Anticarcinogenic and Antimicrobial Response of Synthesized Tungsten Oxide Nanoparticles

In the present study, we fabricated tungsten trioxide nanoparticles (WO3 NPs) from a tungsten complex [W(C13H10NO)3] of ligand N-salicylideneaniline with tungstic acid as the precursor. Nanoparticles were synthesized using the direct thermal decomposition method. These nanoparticles were evaluated for cytotoxicity influence on human breast cancer MCF7 cell line (adenocarcinoma). The observed results suggested that WO3 can destroy 50 % of viable cells after 24 h of incubation at 37 °C. Based on these results, we concluded that WO3 nanoparticles could be a potential drug carrier candidate against human breast cancer cells based on the amount of the drug. In addition, WO3 nanoparticles exhibited significant antimicrobial and antifungal activity.

Effect of WO3 Nanoparticles on the Radiative Attenuation Properties of SrTiO3 Perovskite Ceramic

In the present work, an experimental study is performed to study the radiation shielding characteristics of SrTiO3 (STO) perovskite ceramic added with different amounts (x = 0, 2, 5, and 10%) of tungsten trioxide nanoparticles (WO3 NPs). The four ceramic samples were prepared using the solid-state reaction method. The structural properties were examined using X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR) techniques. The analysis showed the successful formation of WO3- doped STO samples. The crystallite size, estimated using the Scherrer equation, was found in the range of 50.86–41.17 nm. The effect of WO3 NPs on the radiation shielding performance of these ceramics was studied. Different parameters, such as linear attenuation coefficient (LAC) and other related factors, were experimentally determined. The linear attenuation coefficient results demonstrated that the additional amount of WO3 in the ceramics correlates with an improvement in their shielding abilities. The half-value layer (HVL) values for the ceramics with 2% WO3 nanoparticles are equal to 0.071, 1.760, 2.407, and 2.564 cm at 0.060, 0.662, 1.173, and 1.333 MeV, respectively. As the energy increases, more radiation can pass through the material; therefore, a larger thickness is required to absorb half of the total photons, leading to a greater HVL. The tenth value results reaffirmed that increasing the WO3 content in the STO ceramics improves their shielding efficiency. The radiation protection efficiency (RPE) of the four prepared STO ceramics was reported. From the RPE, we found that more photons can be attenuated at lower energies.