Tungsten Oxide Research Articles

Thixotropic Composite Hydrogel Electrode Composed of a Polymer Hydrogelator and Water-Dispersive Tungsten Oxide Flat Microparticles.

Here, we introduce an organic/inorganic composite hydrogel as a versatile gel electrode material. This composite hydrogel was formed by simply mixing an aqueous solution of flat microparticles of tungsten oxide, exhibiting superior water dispersibility, with a hydrogel composed of a water-soluble polyaramide-based polymer hydrogelator. The resulting composite hydrogel exhibited uniform dispersion of tungsten oxide flat particles throughout the hydrogel matrix, supplementing the structure formed by the polymer hydrogelator. It maintained the gel-forming capability and thixotropic behavior inherent to the polymer hydrogelator while showcasing the electrochemical characteristics of tungsten oxide. With its spreadability and applicability to various electrode shapes, a composite hydrogel is presented as a potential spreadable gel electrode material.

Observations on “Mg” incorporated oxides of tungsten for superconducting applications

The present work involves in the synthesis and characterization of pristine and "Mg" associated WO3.H2O nano powders by a high yield irradiation technique using microwaves. The diffraction patterns present phased orthorhombic phase and retained even after annealing process. Clear evidence noticed for pure and doped samples in morphological behavior of the samples. The change in optical properties in terms of energy values revealed the contribution of dopants with the evident at 360 nm wavelength blue shift. The obtained magnetic behavior on the annealed samples revealed the transition offer magnetic state to diamagnetic state may be investigated for super conducting applications.

Laser-Printed Photoanode: Femtosecond Laser-Induced Crystalline Phase Transformation of WO3 Nanorods for Space-Efficient and Flexible Thin-Film Solar Water-Splitting Cells.

Despite its potential for clean hydrogen harvesting, photoelectrochemical (PEC) water-splitting cells face challenges in commercialization, particularly related its harvesting performance and productivity at an industrial scale. Herein, a facile fabrication method of flexible thin-film photoanode for PEC water-splitting to overcome these limitations, based on laser processing technologies, is proposed. Laser-induced graphene, a carbon structure produced through direct laser writing carbonization (DLWC), plays a dual role: a flexible and stable current collector and a substrate for the hydrothermal synthesis of tungsten trioxide (WO3) nanorods (NRs). To facilitate water-splitting, a femtosecond-pulsed laser (fs laser) is focused on the WO3 NRs, converting their crystalline phase from pristine orthorhombic to monoclinic structure without thermal damage. With NiFe layered double hydroxide (LDH) catalyst, the flexible thin-film photoanode exhibits good PEC performance (1.46mAcm-2 at 1.23 VRHE) and retains ≈90% of its performance after 3000 bending cycles. With its excellent mechanical properties, the flexible photoanode can be operated in various shapes with different curvatures, enabling space-efficient PEC water-splitting by loading larger photoanode within a given space. This study is expected to contribute to the advancement of large-scale solar water-splitting cells, introducing a new approach to enhance H2/O2 production and expand its application range.

Scalable decarboxylative trifluoromethylation by ion-shielding heterogeneous photoelectrocatalysis

Electrochemistry offers a sustainable synthesis route to value-added fine chemicals but is often constrained by competing electron transfer between the electrode and redox-sensitive functionalities distinct from the target site. Here, we describe an ion-shielding heterogeneous photoelectrocatalysis strategy to impose mass-transfer limitations that invert the thermodynamically determined order of electron transfer. This strategy is showcased to enable decarboxylative trifluoromethylation of sensitive (hetero)arenes by using trifluoroacetate, an inexpensive yet relatively inert trifluoromethyl group (CF 3 ) source. An ion-shielding layer, formed by trifluoroacetate anions electrostatically adsorbed on a positive molybdenum-doped tungsten trioxide (WO 3 ) photoanode, prevents undesired electron transfer between substrates and photogenerated holes. The practicality of the developed method was demonstrated with robust photoanode stability (approximately 380 hours), a good substrate scope, and scaling capability to achieve 100-gram synthesis by using photoelectrochemical flow cells.

Advanced IGZO Phototransistor Arrays: Enhancing Visible Light Detection Through Selectively Electrohydrodynamic Jet‐Printed Photocatalytic Layer Formation

AbstractExploring new horizons in phototransistors with an emphasis on mass customization is essential. Herein, a method for enhancing the performance of indium‐gallium‐zinc‐oxide (IGZO) phototransistors by incorporating a selectively formed tungsten trioxide (WO3) photocatalytic layer, utilizing electrohydrodynamic (EHD) jet‐printing is proposed. This approach aims to achieve significant manufacturing advantages and enhance functionality. An oxidizing solution of hydrogen peroxide (H2O2) doped with hydroxyethyl cellulose (HEC) is introduced to selectively oxidize tungsten (W) electrodes. In this mixture, H2O2 is responsible for the selective oxidation of W, whereas HEC contributes to the viscosity regulation and the formation of subgap states. The resulting selectively oxidized photocatalytic layer significantly expands its visible light absorption capacity to red light. Therefore, the optimized device, particularly under red light (635 nm) 5 mW mm−2, shows a remarkable enhancement in its optoelectronic characteristic: photoresponsivity increases from 29.71 to 124.54 A W−1, photosensitivity from 1.99 × 10‐1 to 1.79 × 104, and detectivity from 1.31 × 107 to 1.98 × 108 Jones compared to IGZO phototransistors without selectively oxidized photocatalytic layer. This advancement not only enhances the visible light detection capacity but also minimizes the persistent photoconductance issue inherent in IGZO devices. The demonstration of 6 × 6 phototransistor array illustrates the potential for image sensor applications, showcasing the practicality of mass customization.

Integrating Electrochemically Grown Nano‐Oxide and Polymer Films for Electrochromic Device: Achieving Near‐Infrared Shielding and Four‐Digit Efficiency

Electrochemically deposited thin films yield high uniformity, a property which is quite vital to in the context of electrochromic (EC) coatings and devices. Tungsten oxide and polyaniline are two such materials that show superior EC properties individually. However, when combined into a solid‐state device structure, they yield a device where the efficiency increases multifolds. This device combination, being thoroughly characterized in the domain of EC parameters such as high switching speeds, rich color contrast, and stability, is found to be an excellent complementary EC pair. The unique property of the said device is that it can reduce the transmission of wavelengths in the near‐infrared region of the electromagnetic spectrum, providing an edge over other such combinations. In addition, a four‐digit value of coloration efficiency makes this device stand out in the family of its contemporaries. Overall, the hybrid nature of the device prompts it to be an excellent combination indicating its high performance in terms of increased endurance and heat isolation capacity.

Constructing High-Active Surface of Plasmonic Tungsten Oxide for Photocatalytic Alcohol Dehydration.

Plasmonic semiconductors with broad spectral response hold significant promise for sustainable solar energy utilization. However, the surface inertness limits the photocatalytic activity. Herein, a novel approach is proposed to improve the body crystallinity and increase the surface oxygen vacancies of plasmonic tungsten oxide by the combination of hydrochloric acid (HCl) regulation and light irradiation, which can promote the adsorption of tert-butyl alcohol (TBA) on plasmonic tungsten oxide and overcome the hindrance of the surface depletion layer in photocatalytic alcohol dehydration. Additionally, this process can concentrate electrons for strong plasmonic electron oscillation on the near surface, facilitating rapid electron transfer within the adsorbed TBA molecules for C-O bond cleavage. As a result, the activation barrier for TBA dehydration is significantly reduced by 93% to 6.0kJ mol-1, much lower than that of thermocatalysis (91kJ mol-1). Therefore, an optimal isobutylene generation rate of 1.8mol g-1 h-1 (selectivity of 99.9%) is achieved. A small flow reaction system is further constructed, which shows an isobutylene generation rate of 12mmol h-1 under natural sunlight irradiation. This work highlights the potential of plasmonic semiconductors for efficient photocatalytic alcohol dehydration, thereby promoting the sustainable utilization of solar energy.

Preparation and characterization of composite-modified PA6 fiber for spectral heating and heat storage applications

Abstract Composite coating technology was used to prepare a modified polyamide 6 (PA6) polymer material masterbatch with low mutual interference and good spinnability using molybdenum oxide, tungsten trioxide, graphene oxide, etc., as modifiers. Experiment shows that using nanoscale composite-coated modified masterbatches capable of spectral heating and heat storage in the preparation of nylon 6 fiber, adding modified masterbatches with a mass ratio of 6% online, and controlling various process parameters can result in good functionality and usability as well as enable consistent production. Optimal production conditions are achieved by utilizing pre-dried PA6 chips with a moisture content of 420 ppm. The master batch is subjected to drying at a temperature of 95°C for 12 h. During this process, the master batch is introduced at an addition ratio of 6%. Subsequent spinning is conducted at a speed of 4,300 m·min−1 and a temperature of 255°C. Cooling is facilitated by air set at a temperature of 17°C, flowing at a speed of 0.45 m·min−1. In the production line, one roller operates without heating, while the second roller is maintained at a temperature range of 160°C. The stretching process is performed at a ratio of 1.3. To ensure proper lubrication, an oil rate of 1.3% is applied. These meticulously controlled process parameters collectively contribute to the most favorable production status.

Effect of In Situ Heating on the Growth and Electrochromic Properties of Tungsten Trioxide Thin Films

Electrochromism has emerged as a pivotal technology in the pursuit of energy efficiency and environmental sustainability, spurring significant research efforts aimed at the creation of advanced electrochromic devices. Most electrochromic materials are used for smart window applications. However, current electrochromic materials have been applied to new energy vehicles, cell phone back covers, AR glasses, and so on. More application scenarios put forward more requirements for the color of the colored states. Choosing the right color change in the application will be the trend in the future. In this work, tungsten trioxide (WO3) thin films were prepared by adjusting the in situ heating temperature. WO3 with a crystalline structure showed excellent cyclic stability (5000 cycles), electrochromic performance (ΔT = 77.7% at 633 nm, CE = 37.1 cm2/C), relatively fast bleaching/coloring speed (20.0 s/19.4 s), and the darkest coloring effect (L* = 29.32, a* = 7.41, b* = −22.12 for the colored state). These findings offer valuable insights into the manipulation of smart materials and devices, contributing to the advancement of electrochromic technology.

Transition metal oxide catalytic abilities for fuel cell applications: Density functional theory (DFT) studies

Because of its heavy reliance on fossil fuels, the world's existing energy supply releases pollutants into the atmosphere. Researchers have conducted extensive studies on greener energy sources, particularly fuel cell technology, which generates power from electrochemical energy while emitting minimal carbon. But there are obstacles to fuel cell efficiency and commercialization, such as the slow oxygen reduction reaction (ORR) and the expensive and unstable platinum (Pt) catalysts used in fuel cell membranes. This work explores the use of tungsten oxide, cobalt, and titanium oxide nanoparticles as inexpensive, active electrocatalysts. Despite extensive research on the monoxides of these metals, their bimetallic compositions when combined with oxygen to function as fuel cell catalysts remain poorly understood. This work evaluates the catalytic capabilities of the crystallographic surfaces of these oxides using Density Functional Theory (DFT) via CASTEP and DMol3, as well as the Adsorption Locator module. These surfaces, which include CoWO4, Co3WO8, and TiWO4, have different levels of stability and reactivity when it comes to absorbing hydrogen and oxygen. This makes them potentially useful for changing the hydrogen oxidation and oxygen reduction reactions in fuel cells.

Defective Tungsten Oxides with Stacking Faults for Proton Exchange Membrane Green-Hydrogen Generation.

Defects can introduce atomic structural modulation and tailor performance of materials. Herein, it demonstrates that semiconductor WO3 with inert electrocatalytic behavior can be activated through defect-induced tensile strains. Structural characterizations reveal that when simply treated in Ar/H2 atmosphere, oxygen vacancies will generate in WO3 and cause defective structures. Stacking faults are found in defects, thus modulating electronic structure and transforming electrocatalytic-inert WO3 into highly active electrocatalysts. Density functional theory (DFT) calculations are performed to calculate *H adsorption energies on various WOx surfaces, revealing the oxygen vacancy composition and strain predicted to optimize the catalytic activity of hydrogen evolution reaction (HER). Such defective tungsten oxides can be integrated into commercial proton exchange membrane (PEM) electrolyser with comparable performance toward Pt-based PEM. This work demonstrates defective metal oxides as promising non-noble metal catalysts for commercial PEM green-hydrogen generation.

Electrochromic screen-printed tungsten trioxide electrodes

A methodology is presented to develop tungsten-oxide based inks for screen-printing. Different amounts of tungsten oxide have been grown by co-precipitation on the surface of conducting microparticles. These modified particles have been formulated into inks, and electrodes have been screen-printed. The work describes the characterization of the materials using a range of techniques including XRD, SEM, as well as electrochemical and spectroscopic techniques. Thermal treatment of the co-precipited oxides changes their crystalline structure, increasing bandgap (from 2.48 eV to 2.87 eV) and worsening their electrochromic performance. Structures printed with untreated WO3-based materials display contrast ratios as high as 90 % in reflectance, and colour efficiencies between 30 and 40 cm2 C–1. Another important aspect is the pH stability of the oxide up to pH = 6.

Tungsten Oxide Dispersed on Silica as Robust and Readily Available Oxo/Imido Heterometathesis Catalyst.

Continuing our investigation of catalytic oxo/imido heterometathesis as novel water-free method for C=N bond construction, we report here the application of classical transition metal oxides dispersed on silica (MOx/SiO2, M=V, Mo, W) as cheap, robust and readily available alternative to the catalysts prepared via Surface Organometallic Chemistry (SOMC). The oxide materials demonstrated activity in heterometathetical imidation of ketones, WO3/SiO2 being the most efficient. We also describe a new well-defined supported W imido complex (≡SiO)W(=NMes)2(Me2Pyr) (Mes=2,4,6-Me3C6H2, Me2Pyr=2,5-dimethylpyrrolyl) and characterize it with SOMC protocols, which allowed us to identify the position of W on the oxo/imido heterometathesis activity scale (Mo<W<Ta) and showed that W in fact provides an optimal balance between activity and stability. Noteworthy, the performance of WO3/SiO2 was only slightly inferior to that of the SOMC analog enabling the efficient synthesis of a broad range of ketimines hardly accessible by classical methods, in most cases W being a competitive and robust alternative to the most active albeit highly sensitive Ti imido systems. Combined with the availability of the catalyst, this facilitates a more widespread application of heterometathesis methodology in organic synthesis including potential larger scale applications.

Design tungsten oxides hole transport layers (HTLs) to modify the back interface in all-inorganic carbon-based CsPbBr3 solar cells

To enhance the inferior photovoltaic performance of all-inorganic carbon-based perovskite solar cells (C-PSCs) caused by inefficient charge extraction and transport processes of the CsPbBr3/carbon back interface, three types of tungsten oxides (WO3, WO2.72, WO2) are synthesized as low cost and stable hole transport layers (HTLs) to modify the back interface by tunning the energy level alignment. Among the three kinds of tungsten oxides, WO3 shows the best hole extraction and transport capability and the C-PSCs using WO3 HTL generates a power conversion efficiency (PCE) of 7.90% with a high open circuit voltage (Voc) of 1.307 V, indicating a great PCE enhancement of 43.9%, as compared with the device without HTL (5.49%). Meanwhile, WO2.72 and WO2 also are also proved to be qualified HTLs and the devices show PCE values of 7.57% and 6.24%, respectively. Importantly, WO3 and WO2.72 based device show excellent stabilities with PCE retention over 90% of the initial PCE values under ambient conditions for 60 days.

Investigation the Gamma Ray Shielding Parameters for Portland Cement Doped with Several Metal Oxides

In this research, gamma ray photons emitted from radioactive sources (Cs-137, Ra-226) with energies (186, 242, 295, 352, 609, 662, 1120, 1765) keV, respectively, to study some parameters, Such as the linear attenuation coefficient ( , mass attenuation coefficient ( for shield made of composite materials consisting of cement as the base material reinforced with different materials (magnesium oxide MgO , tungsten oxide WO3) nanoparticles with different reinforcement ratios (10, 30, 50) % and thickness (0.5) cm to protect against radiation. For this purpose, a sodium iodide detector activated with thallium with dimensions ( was used with an integrated measuring system, to determine the suitability of these shields for use in the field of gamma ray protection. The results showed that the values ​​of these parameters are affected by changing the reinforcement ratios and the gamma ray energy. It was found that when increasing the reinforcement ratio of the shield led to an increase in the linear and mass attenuation coefficient, and in contrast, a decrease in the values ​​of each occurs when the gamma ray energy of the used radioactive source is increased, especially at a concentration of 50 % and at energy (1765) Kev.

Glutathione-Mediated Synthesis of WO3 Nanostructures with Controllable Morphology/Phase for Energy Storage, Photoconductivity, and Photocatalytic Applications.

Developing an improved synthesis method that controls the morphology and crystal phase remains a substantial challenge. Herein, we report phase and morphology-controlled hydrothermal synthesis of tungsten oxides by varying acid concentration and utilizing glutathione (GSH) as a structural directing agent, together with the exploration of their applications in supercapacitors, photoconductivity, and photocatalysis. Orthorhombic hydrated tungsten oxide (WO3·0.33H2O) with nonuniform block and plate-like morphology was obtained at 3 M hydrochloric acid (HCl). In contrast, nonhydrated monoclinic tungsten oxide (WO3) with smaller rectangular blocks was obtained at 6 M HCl. Further, the addition of GSH results in an increase in the surface area of the materials along with a narrowing of the band gap. Moreover, it plays a pivotal role in regulating the morphology through oriented attachments, Ostwald ripening, and the self-assembly of WO3 nuclei. GHTO and GTO polymorphs showed pseudocapacitive behavior with the highest specific capacitances of 450 and 300 F g-1 at 0.5 A g-1, maintaining 94 and 92% retention stability, respectively, over 1000 cycles at 2 A g-1. Also, the synthesized materials displayed favorable photoconductivity under light irradiation, implying potential utilization in photovoltaic applications. Moreover, these materials exhibited remarkable photocatalytic performance in the degradation of methylene blue (MB) dye, establishing themselves as highly effective photocatalysts. Therefore, nanostructured tungsten oxide showcases its versatility, rendering it an appealing candidate for energy storage, photovoltaic systems, and photocatalysis.

Photoelectrochemical Conversion of Methane to Ethane and Hydrogen under Visible Light Using Functionalized Tungsten Trioxide Photoanodes with Proton Exchange Membrane.

Developing methane utilization technologies is desired to convert abundant and renewable carbon resources, such as natural gas and biogas, into value-added chemical products. This study provides insights into emerging photoelectrochemical (PEC) technology for the photocatalytic transformation of methane to C2H6 and H2 using visible light at room temperature. The PEC conversion of methane to oxygenates has been investigated in aqueous electrolytes. Herein, we demonstrate the gas-phase PEC methane conversion using a proton exchange membrane (PEM) as a solid polymer electrolyte and a gas-diffusion photoanode for methane oxidation. Tungsten trioxide (WO3), a semiconductor photocatalyst responsive to visible light, is utilized as the photoanode material. Ultraviolet light (∼365 nm) excitation predominantly results in CO2 production with lower C2H6 selectivity in humidified methane. In contrast, visible light (∼453 nm) effectively promotes C2H6 production over the WO3 photoanode, attributed to preferential hydroxyl radical (•OH) formation compared to UV irradiation. Photogenerated holes formed near the valence band maximum of WO3 contribute to •OH formation through a single-electron water oxidation. The photogenerated •OH activates gaseous methane molecules to methyl radicals, subsequently coupled into C2H6 at the gas-electrolyte-semiconductor boundary. H2 is concurrently formed on the cathode electrocatalyst. Improving the selectivity for the dehydrogenative coupling of methane is pivotal for enhancing the energy efficiency in the PEM-PEC system.

Nanostructured tungsten trioxide developed from environmentally friendly green process as a promising cathode for excellent field emission

Extensively explored as cathodes for field emission, nanostructured metal oxides play a crucial role in diverse applications such as microwave amplifiers, renewable energy systems, flat panel displays, and micro-electronics. The quest for high current density, low threshold field, and stable field emission persists. In present study, we introduce a green synthesis approach using vegetable oil as a reaction medium to produce hexagonal tungsten trioxide (h-WO3). The structural analysis confirmed the formation of h-WO3 with a nanorod-like morphology. The spin-coated h-WO3 film on a silicon substrate exhibited promising field emission properties, including a field enhancement factor (β) of 1596 and a turn-on field of 4.60 V/μm, comparable to reported values. This research opens avenues for the cost-effective and scalable utilization of h-WO3 as an electron emitter in advanced optical and electrical devices.

Electrochemical Properties of NiCo2O4/WO3/Activated Carbon Wheat Husk Nano-Electrocatalyst for Methanol and Ethanol Oxidation

It is common to use efficient catalysts in the anodes and cathodes of methanol and ethanol fuel cells, such as platinum and ruthenium. However, due to their expansivity and rarity, finding a suitable alternative is important. In this work, multi-component catalysts consisting of tungsten oxide, nickel cobaltite, and activated carbon were synthesized through the hydrothermal method. The performance of catalysts in the processes of methanol and ethanol oxidation reactions (MOR and EOR) were investigated. The addition of activated carbon obtained from wheat husk, with an excellent active surface and acceptable electrical conductivity, to the matrix of the catalyst significantly facilitated the oxidation process of alcohols and enhanced the efficiency of the catalyst. The physical and electrochemical characterization of the NiCo2O4/WO3 hybridized with the wheat husk-derived activated carbon (ACWH) catalyst indicated its successful synthesis and good performance in the alcohol oxidation process. NiCo2O4/WO3/ACWH with an oxidation current density of 63.39 mA/cm2 at the peak potential of 0.58 V (1.59 vs. RHE), a cyclic stability of 98.6% in the methanol oxidation reaction (MOR) and 27.98 mA/cm2 at the peak potential of 0.67 V (1.68 vs. RHE), and a cyclic stability of 95.7% in the ethanol oxidation reaction (EOR) process can be an interesting option for application in the anodes of alcohol fuel cells.

Metal oxide-based nanocomposites as advanced electrode materials for enhancing electrochemical performance of Supercapacitors: A comprehensive review

In recent years, the escalating use of nonrenewable fossil fuels has emerged as a significant threat to global sustainability, prompting the need for renewable, cost-effective, and eco-friendly energy storage solutions. Supercapacitors (SCs) are notable for their high power density (PD), cycle stability, and swift charge/discharge rates, although they fall short in energy density (ED) compared to traditional batteries. The performance of SCs is greatly influenced by the electrode materials used, highlighting the importance of material innovation in tackling the challenges posed by increasing fossil fuel consumption. Transition metal oxides (TMOs), known for their redox activity in energy storage, have been thoroughly investigated for their exceptional specific capacitance, which ranges from 100 to 2000F g−1, surpassing that of electrical double-layer capacitors (EDLCs). TMOs such as ruthenium oxide (RuO2), manganese oxide (MnO2), nickel oxide (NiO), cobalt oxide (Co3O4), tin oxide (SnO2), zinc oxide (ZnO), tungsten oxide (WO3), and vanadium pentoxide (V2O5) are widely researched for their high theoretical capacitance, affordability, and longevity. This review emphasizes the groundbreaking potential of metal oxide nanocomposites (NCs) formed by combining them with graphene, carbon nanotubes (CNTs), and polymers, leading to synergistic enhancements in electrical conductivity, surface area, and charge storage capacity. This thorough review not only presents an in-depth analysis of current research but also sheds light on potential future developments, contributing to the ongoing progress in the field of advanced electrode materials for energy storage.