Search Results (58)

Ammonia, a toxic and volatile pollutant commonly found in chemical industrial environments, requires reliable real-time detection to ensure industrial safety and effective environmental monitoring. Conventional gas sensors typically operate at elevated temperatures, resulting in high power consumption. Moreover, pure metal oxides and conductive polymers often suffer from significant aggregation and exhibit suboptimal sensing performance under ambient conditions, limiting their practical applications. In this study, hierarchical porous V₂O₅/PANI composites were synthesized via a straightforward one-step coprecipitation method combined with in situ polymerization. The interlaced architecture of polyaniline (PANI) and vanadium pentoxide (V₂O₅) effectively reduces structural aggregation and increases the availability of surface active sites. Furthermore, the synergistic interaction at the bi-phase interface significantly enhances charge carrier transport, leading to improved ammonia-sensing capabilities at room temperature. Notably, the composite containing 20% V₂O₅ demonstrated superior response, selectivity, and reproducibility toward 10 ppm NH₃. Due to its simple fabrication process and room-temperature operation without external heating, the developed V₂O₅/PANI composite sensor holds significant potential for practical applications in low-concentration ammonia detection under ambient conditions. Full article

Aluminum alloy 6061 is widely used in the industrial field, but its poor corrosion resistance has a significant impact on the reliability of equipment components. To address the corrosion resistance issue of 6061 aluminum alloy, a novel Ti-Zr-V conversion coating was prepared on its surface in this study, and the conversion parameters were optimized. The morphology, element distribution and content, composition of compounds, and corrosion resistance of the prepared Ti-Zr-V conversion coating were comprehensively analyzed and evaluated using scanning electron microscopy, energy dispersive spectroscopy, X-ray photoelectron spectroscopy, copper sulfate spot test, and electrochemical experiments. The research results showed that the conversion parameters had a significant impact on the corrosion resistance of the conversion coating. The optimal conversion parameters were a pH value of 4.5 and a conversion time of 5 min, with the optimal addition amount of the auxiliary film former NaVO₃ being 0.6 g/L. Under these conditions, the Ti-Zr-V conversion coating prepared was relatively dense, with fewer grooves, the longest spot resistance time, and the best corrosion resistance. Its surface mainly consisted of titanium dioxide, zirconium dioxide, vanadium pentoxide, V₂O₃, aluminum oxide, and a small amount of fluoride compounds. Electrochemical analysis also demonstrated that the corrosion rate of TiZrVCC decreased by approximately 87.12% compared to the aluminum alloy 6061 substrate, providing a theoretical basis and technical support for the further promotion and use of aluminum alloy. Full article

The hydrogen evolution reaction (HER) plays a pivotal role in electrochemical water splitting for sustainable hydrogen production. However, its practical implementation is hindered by sluggish kinetics and the reliance on costly noble-metal catalysts. In this work, a conductive polymer-inorganic hybrid electrode based on vanadium pentoxide (V₂O₅) and polyaniline (PANI) is rationally designed and fabricated on carbon cloth via a combined hydrothermal synthesis and electropolymerization strategy. Initially, hierarchical V₂O₅ nanoflowers were synthesized, followed by controlled PANI deposition through cyclic voltammetry at varying cycle numbers to tailor the interfacial architecture and electronic properties. Morphological and structural analyses reveal the formation of well-defined V₂O₅ nanoflowers uniformly decorated with PANI nanorods, establishing an interconnected conductive network. Among the prepared samples, the optimized V₂O₅-PANI-2 electrode exhibits superior interfacial integration and structural homogeneity. Electrochemical evaluation in 1.0 M KOH demonstrates that V₂O₅-PANI-2 achieves a low overpotential of 79.9 mV at −10 mA cm⁻², accompanied by a small Tafel slope of 46.6 mV dec⁻¹, indicating accelerated HER kinetics. Furthermore, the electrode shows reduced charge-transfer resistance and an enhanced electrochemically active surface area (ECSA), facilitating efficient charge transport and abundant active site exposure. The catalyst also delivers excellent durability, maintaining stable performance over 5000 CV cycles and prolonged 24 h operation. The enhanced HER performance is attributed to the synergistic interaction between V₂O₅ and the conductive PANI matrix, which promotes charge redistribution, improves electrical conductivity, and optimizes the adsorption/desorption energetics of hydrogen intermediates. Full article

This article describes a study on the synthesis and annealing processes of thin-film coatings of vanadium oxide on flat, parallel substrates made of quartz glass, sapphire, and silicon, as well as optical fibers using an organometallic precursor, triisopropoxy vanadium (V) oxide. For the first time, optical constants of nanomaterials were estimated in real time during synthesis and subsequent annealed using the lossy-mode resonance effect. The coatings produced in an inert atmosphere after deposition were amorphous, comprising a mixture of VO₂, V₂O₅, V₆O₁₃, and V₃O₅. This method allowed for accurate determination of the threshold temperature for the transformation of oxide mixtures into a monocomponent phase. Optimal conditions for synthesis and annealing were determined for the production of vanadium dioxide (VO₂) and pentoxide (V₂O₅). Morphological changes in coated surfaces were observed as a result of heat treatment. The composition and properties of these samples were studied using optical, terahertz and Raman spectroscopy, as well as temperature-dependent analysis of electrical resistance. The morphology of the coating surface was determined using a scanning electron microscope and an atomic force microscope. The reduction of VO_x to VO₂ was studied in an atmosphere of hydrogen and argon during annealing after deposition, with its effectiveness being compared. It was shown for the first time that the reduction of higher vanadium oxides is due to the presence of elemental carbon in the volume of the material formed from a metalorganic precursor during growth of vanadium oxide. Coatings obtained by annealing in hydrogen had a smaller hysteresis loop width (~5 °C) during phase transition compared to coatings obtained by argon annealing (~9 °C). Both types of coatings demonstrated a 50–60% increase in transmission at 1 THz frequency and in the IR region, accompanied by a 10³–10⁴-fold change in electrical resistance. Full article

Cyclodextrins in metal oxide nanoparticles (NPs) serve as stabilizing, dispersing, and functionalizing agents that enhance antimicrobial performance through better nanoparticle stability, synergistic action, and potential controlled release mechanisms, making them ideal for advanced biomedical and environmental antimicrobial applications. In this study, NPs of vanadium pentoxide (V₂O₅) were obtained by the precipitation method, and, following a supramolecular assembly, were synthesized using the impregnation method via addition of β-cyclodextrin (BCD) and its derivatives, such as hydroxypropyl-β-cyclodextrin (HCD) and methyl-β-cyclodextrin (MCD). The formation of the V₂O₅:CDs was driven by non-covalent host–guest interactions, leading to a stable supramolecular structure with enhanced physicochemical properties. Morphological analysis using scanning electron microscopy (SEM) revealed uniformly distributed V₂O₅ NPs within the CD matrix. Structural characterization was further supported by proton nuclear magnetic resonance (NMR) spectroscopy, which confirmed the inclusion interactions between V₂O₅ and CDs. The synthesized NPs demonstrated significant antimicrobial activity against Gram-positive and fungal strains, indicating a synergistic enhancement in bioactivity due to the supramolecular architecture. This work highlights the potential of CD-assisted V₂O₅ NPs as promising antimicrobial agents for biomedical and environmental applications. Full article

Layered intercalating V₂O₅ (vanadium pentoxide) is a durable battery-type electrode material exploited in supercapacitors. The advancement of V₂O₅ nanomaterials synthesized from non-aqueous organic solvents holds significant potential for energy storage applications. Liquid-phase synthesis of orthorhombic V₂O₅ cathode material corroborated its compatibility with quartet glycols and allowed examination of their explicit roles in faradic charge storage efficacy. V₂O₅ was found to be an intercalative material in all the quartet glycols. The crystalline, rod-like morphology and monodisperse V₂O₅ electrode were ascribed to the effects of ethylene, diethylene, triethylene, and tetraethylene glycols. Notable differences were observed in the electrochemical analysis of the prepared V₂O₅ (EV, DV, TV, and TTV). In a three-electrode cell setup, the DV electrode demonstrated a superior specific capacity of 460.2 C/g at a current density of 1 A/g. From the Trasatti analysis, the DV electrode exhibited 961.53 C/g of total capacitance, comprising a diffusion-controlled contribution of 898.19 C/g and a surface-controlled contribution of 63.34 C/g. The aqueous asymmetric device DV//AC exhibited a maximum energy density of 65.72 Wh/kg at a power density of 1199.97 W/kg. The glycol-derived electrodes were anticipated to bepromising materials for supercapacitors and have the potential to meet electrochemical energy needs. Full article

Vanadium pentoxide (V₂O₅) has attracted considerable interest owing to its unique chemical and physical properties. However, traditional synthesis methods are often time-consuming, complex, and difficult to scale, limiting the broader applications of V₂O₅. Herein, we present a flame vapor deposition (FVD) method to enable rapid, scalable, and one-step synthesis of various V₂O₅ nanostructures under ambient pressure conditions. By optimizing critical synthesis parameters, specifically, source temperature (840 °C) and substrate temperature (610 °C), we achieved highly crystalline, one-dimensional (1D) V₂O₅ nanorods on a variety of substrates, including silicon (Si), fluorine tin doped (FTO) glass, stainless steel, and silicon dioxide (SiO₂). Moreover, we demonstrate the rapid growth of ultrathin, two-dimensional (2D) V₂O₅ nanoflakes with nanometer-scale thickness, as well as enhanced uniformity and coverage density with an externally applied electric field. This FVD method provides a simple, efficient, and scalable approach for synthesizing advanced V₂O₅ nanostructures, significantly expanding opportunities for their integration into various technological applications. Full article

This study reports an efficient and low-cost hydrothermal method for synthesizing vanadium oxide/graphene nanocatalysts. Field-emission scanning electron microscopy (FESEM) revealed the formation of nanostructured catalysts with consistent and directional shapes, as confirmed by X-ray diffraction (XRD). Fourier transform infrared (FTIR) spectroscopy indicated the presence of V₂O₅ and graphene, highlighting their bonds and structures. Thermogravimetric analysis (TGA) identified three stages of weight loss in the nanocatalysts, corresponding to water molecule evaporation, decomposition of residual organics, and the formation of yellow vanadium pentoxide particles due to the oxidation of vanadium V⁴⁺. Gas chromatography analysis from 450 °C to 600 °C showed that ethylene selectivity increased with temperature, while propylene selectivity showed the opposite trend. The effectiveness of these nanocatalysts was assessed in the oxidative dehydrogenation of propane using temperature programmed reduction. The approach of graphene-based vanadium oxide nanostructures will open up a new insight into the fabrication of high-performance catalysts. Full article

We report a gas-phase precursor modulation strategy for the controlled synthesis of 1T-phase vanadium diselenide (VSe₂) from vanadium pentoxide (V₂O₅) nanosheets by systematically adjusting the vapor pressure of selenium. By controlling the selenium vapor pressure, selenium-free vapor transport of vanadium dioxide led to the spontaneous oxidation and formation of tens-of-micrometer-sized rectangular V₂O₅ crystals, while moderate selenium introduction produced intermediate oxygen-rich phases with trapezoidal crystal facets, and a highly selenium-rich environment yielded trigonal VSe₂ crystals. Raman scattering measurements confirmed the stepwise transformation from V₂O₅ to VSe₂, and atomic force microscopy revealed well-defined layered morphologies and distinct conformation within an atomically thin regime. Additionally, high-resolution transmission electron microscopy validated the orthorhombic and trigonal crystal structures of V₂O₅ and VSe₂, respectively. This work demonstrates the versatility of fine-tuned vapor-phase growth conditions in vanadium-based layered compounds, providing useful platforms to optimize structural composition with atomic precision. Full article

In this study, vanadium (3.5⁺) electrolyte was prepared for vanadium redox flow batteries (VRFBs) through a reduction reaction using a batch-type hydrothermal reactor, differing from conventional production methods that utilize VOSO₄ and V₂O_5. The starting material, V₂O₅, was mixed with various concentrations (0.8 M, 1.2 M, 1.6 M, 2.0 M) of citric acid (CA) as the reducing agent and stirred for 60 min at 90 °C using a hot plate to ensure complete dispersion in the solution. The resulting solution was subsequently subjected to a hydrothermal reduction reaction (HRR) furnace at 150 °C for 24 h to generate vanadium (3.5⁺). The mixed states of the produced vanadium (3⁺) and vanadium (4⁺) were confirmed using UV-vis spectroscopy. The electrochemical properties of the electrolyte were investigated through cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS), revealing that the optimal concentration of the CA was 1.6 M. The current efficiency, energy efficiency, and voltage efficiency of the electrolyte produced via the HRR process was compared with that prepared using VOSO₄ in charge and discharge experiments. The results demonstrate that the HRR process yields an enhanced electrolyte across all efficiency metrics produced through the given improved performance in all efficiencies. These findings indicate that the HRR process using citric acid can facilitate the straightforward preparation of vanadium (3.5⁺) electrolyte, making it suitable for large-scale production. Full article

Incorporating metal cations into V₂O₅ has been proven to be an effective method for solving the poor long-term cycling performance of vanadium-based oxides as electrodes for mono- or multivalent aqueous rechargeable batteries. This is due to the existence of a bilayer structure with a large interlayer space in the V₂O₅ electrode and to the fact that the intercalated ions act as pillars to support the layered structure and facilitate the diffusion of charged carriers. However, a fundamental understanding of the mechanical stability of multi-ion-co-intercalated bilayered V₂O₅ is still lacking. In this paper, a variety of pillared vanadium pentoxides with two types of co-intercalated ions were studied. The root-mean-square deviation of the V-O bonds and the elastic constants calculated by density functional theory were used as references to evaluate the stability of the intercalated compounds. The d-band center and electronic band structures are also discussed. Our theoretical results show that the structural characteristics and stability of the system are quite strongly influenced by the intercalating strategy. Full article

Aqueous zinc-ion batteries (ZIBs) have attracted burgeoning attention and emerged as prospective alternatives for scalable energy storage applications due to their unique merits such as high volumetric capacity, low cost, environmentally friendly, and reliable safety. Nevertheless, current ZIBs still suffer from some thorny issues, including low intrinsic electron conductivity, poor reversibility, zinc anode dendrites, and side reactions. Herein, conductive polyaniline (PANI) is intercalated as a pillar into the hydrated V₂O₅ (PAVO) to stabilize the structure of the cathode material. Meanwhile, graphene oxide (GO) was modified onto the glass fiber (GF) membrane through simple electrospinning and laser reduction methods to inhibit dendrite growth. As a result, the prepared cells present excellent electrochemical performance with enhanced specific capacity (362 mAh g⁻¹ at 0.1 A g⁻¹), significant rate capability (280 mAh g⁻¹ at 10 A g⁻¹), and admirable cycling stability (74% capacity retention after 4800 cycles at 5 A g⁻¹). These findings provide key insights into the development of high-performance zinc-ion batteries. Full article

Chronic environmental exposure to toxic heavy metals, which often occurs as a mixture through occupational and industrial sources, has been implicated in various neurological disorders, including Parkinsonism. Vanadium pentoxide (V₂O₅) typically presents along with manganese (Mn), especially in welding rods and high-capacity batteries, including electric vehicle batteries; however, the neurotoxic effects of vanadium (V) and Mn co-exposure are largely unknown. In this study, we investigated the neurotoxic impact of MnCl₂, V₂O_5, and MnCl₂-V₂O₅ co-exposure in an animal model. C57BL/6 mice were intranasally administered either de-ionized water (vehicle), MnCl₂ (252 µg) alone, V₂O₅ (182 µg) alone, or a mixture of MnCl₂ (252 µg) and V₂O₅ (182 µg) three times a week for up to one month. Following exposure, we performed behavioral, neurochemical, and histological studies. Our results revealed dramatic decreases in olfactory bulb (OB) weight and levels of tyrosine hydroxylase, dopamine, and 3,4-dihydroxyphenylacetic acid in the treatment groups compared to the control group, with the Mn/V co-treatment group producing the most significant changes. Interestingly, increased levels of α-synuclein expression were observed in the substantia nigra (SN) of treated animals. Additionally, treatment groups exhibited locomotor deficits and olfactory dysfunction, with the co-treatment group producing the most severe deficits. The treatment groups exhibited increased levels of the oxidative stress marker 4-hydroxynonenal in the striatum and SN, as well as the upregulation of the pro-apoptotic protein PKCδ and accumulation of glomerular astroglia in the OB. The co-exposure of animals to Mn/V resulted in higher levels of these metals compared to other treatment groups. Taken together, our results suggest that co-exposure to Mn/V can adversely affect the olfactory and nigral systems. These results highlight the possible role of environmental metal mixtures in the etiology of Parkinsonism. Full article

The fabrication of sponge-like vanadium pentoxide (V₂O₅) nanostructures using vertically aligned carbon nanotubes (VACNTs) as a template is presented. The VACNTs were grown on silicon substrates by chemical vapor deposition using the Fe/Al bilayer catalyst approach. The V₂O₅ nanostructures were obtained from the thermal oxidation of metallic vanadium deposited on the VACNTs. Different oxidation temperatures and vanadium thicknesses were used to study the influence of these parameters on the stability of the carbon template and the formation of the V₂O₅ nanostructures. The morphology of the samples was analyzed by scanning electron microscopy, and the structural characterization was performed by Raman, energy-dispersive X-ray, and X-ray photoelectron spectroscopies. Due to the catalytic properties of V₂O₅ in the decomposition of carbonaceous materials, it was possible to obtain supported sponge-like structures based on V₂O₅/CNT composites, in which the CNTs exhibit an increase in their graphitization. The VACNTs can be removed or preserved by modulating the thermal oxidation process and the vanadium thickness. Full article

Copper metal is a promising anode in aqueous batteries due to its low price, noble reaction potential (0.34 V), high theoretical specific capacity, abundance and chemical stability. However, only a few copper ion storage materials have been reported. Herein, layered vanadium pentoxide is chosen to store copper ions for the first time. Ex situ XRD reveals a unique two phase transition process during cycling. The V₂O₅ electrode shows stable copper ion storage performance. It delivers 91.9 mAh g⁻¹ for the first cycle with a cycle life of as high as 4000 cycles at 1.0 A g⁻¹. This work provides an intriguing copper ion storage material and expands the available options of electrode materials for copper ion storage. Full article