Search Results (65)

Ammonia borane (AB) is recognized as a highly promising material for hydrogen storage owing to its exceptional safety and high hydrogen density, enabling controllable hydrogen release at room temperature through catalytic hydrolysis. The development of efficient catalysts to accelerate this process remains a critical research challenge. In this work, carbon nanotube (CNT)-supported Co-MoO₃ nanoparticles were synthesized through reduction with sodium borohydride. The catalyst with a Co/MoO₃ molar ratio of 1.0:0.1 (denoted as Co₁Mo_0.1/CNTs) showed optimal performance in AB hydrolysis, with a turnover frequency (TOF) of 19.15 mol_H2 mol_cat⁻¹ min⁻¹ and an activation energy (E_a) of 26.41 kJ mol⁻¹. The superior performance of the Co₁Mo_0.1/CNTs catalyst can be ascribed to the efficient proton-transfer promotion by carboxylated carbon nanotubes and the synergistic catalytic effect between Co and Mo in the system. This study offers a viable pathway for constructing high-efficiency noble metal-free catalysts for hydrogen production from AB hydrolysis. Full article

In this work, the influences of the Ar flow-rate and sublimation temperature on the phase composition and morphological structure of the sublimation products of analytical reagent MoO₃ are investigated. The results show that the sublimation products are always composed of thermodynamically stable orthorhombic molybdenum trioxide (α-MoO₃) and metastable monoclinic molybdenum trioxide (β-MoO₃) under different reaction conditions, among which the proportion of β-MoO₃ gradually increases with the increase in Ar flow-rate and the decrease in sublimation temperature. The formation temperature of α-MoO₃ is mainly between 780 K and 847 K, with the particles exhibiting an obvious sheet-like morphology. This work also finds that β-MoO₃ is mainly generated below 500 K; however, due to the co-actions of the deposition of gaseous MoO₃ molecules, the adsorption of Ar molecules, and the collision effect between the different particles, the newly formed β-MoO₃ is more inclined to take a spherical-shaped morphology in order to maintain its lowest energy state. Full article

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

Green diesel is a high-quality biofuel obtained through the transformation of triglycerides into linear alkanes. In order to obtain green diesel, this study investigates the impact of impregnation pH on the surface species of NiMo/Al₂O₃ catalysts in the hydroprocessing of soybean oil. NiMo catalysts supported on Al₂O₃ were synthesized at different pH values (pH = 7 and 9). In the oxide state, solids were characterized by UV-Vis diffuse reflectance, Raman, and FT-IR spectroscopies, and, in the sulfide state, they were characterized by HR-TEM. The results show that the pH of impregnation significantly determines the surface species formed. An impregnation at pH = 7 favors the formation of Ni²⁺_(Oh) and Ni²⁺_(Oh-dis) interacting with non-crystalline molybdenum trioxide, while the formation of Ni²⁺/Al₂O₃, Ni_2+(Oh-dis), and MoO₃ species is favored at pH = 9. These surface species play a fundamental role in the hydrogenolysis and deoxygenation steps. Catalyst impregnated at pH = 7 shows higher activity due to the formation of shorter MoS₂ slabs. This study emphasized the importance of controlling impregnation conditions for optimizing catalyst performance. Full article

The ultrafine MoO₃ powders were prepared by the combination of centrifugal spray drying and calcination in this work. The thermal decomposition behavior of the spherical precursor was studied. The phase constituents, morphologies, particle size, and specific surface areas of MoO₃ powders were characterized at different temperatures. It is found that the decomposition of the precursor is subjected to five stages, and forms different intermediate products, including (NH₄)₈Mo₁₀O₃₄, (NH₄)₂Mo₃O₁₀, (NH₄)₂Mo₄O₁₃, h-MoO₃, and the final product α-MoO₃. Moreover, the decomposition rate equation is established based on the thermal decomposition kinetic parameters of the precursor. With an increase in decomposition temperature, the morphology changes from unclear boundary particles to dispersed flake particles, and the flaky particles exhibit larger sizes, higher crystallinity, and better dispersion, which can be attributed to the mass transfer of gaseous MoO₃ products. Additionally, the MoO₃ particle size decreases progressively, and the specific surface area increases and then decreases. At 500 °C, it can achieve ultrafine flaky MoO₃ powder with the size of thick sheets, with a thickness of about 300 nm and a length of about 1–3 μm. This research can offer an innovative strategy for preparing ultrafine MoO₃ powder. Full article

In order to broaden the working voltage (1.23 V) of aqueous supercapacitors, a high-performance asymmetric supercapacitor with a working voltage window reaching up to 2.1 V is assembled using a nanorod-shaped molybdenum trioxide (MoO₃) negative electrode and an activated carbon (AC) positive electrode, as well as a sodium sulfate–ethylene glycol ((Na₂SO₄-EG) electrolyte. MoO₃ electrode materials are fabricated by adjusting the hydrothermal temperature, hydrothermal time and solution’s pH value. The specific capacity of the optimal MoO₃ electrode material can reach as high as 244.35 F g⁻¹ at a current density of 0.5 A g⁻¹. For the assembled MoO₃//AC asymmetric supercapacitor with a voltage window of 2.1 V, its specific capacity, the energy density, and the power density are 13.52 F g⁻¹, 8.28 Wh kg⁻¹, and 382.15 W kg⁻¹ at 0.5 A g⁻¹, respectively. Moreover, after 5000 charge–discharge cycles, the capacity retention rate of the device still reaches 109.2%. This is mainly attributed to the small particle size of MoO₃ nanorods, which can expose more electrochemically active sites, thus greatly facilitating the transport of electrolyte ions, immersion at the electrolyte/electrolyte interface and the occurrence of electrochemical reactions. Full article

This study utilized semiconductor processing techniques to fabricate patterned silicon (Si) substrates with arrays of inverted pyramid-shaped micro-pits by etching. Molybdenum trioxide (MoO₃) was then deposited on these patterned Si substrates using a thermal evaporation system, followed by two-stage sulfurization in a high-temperature furnace to grow MoS₂ thin films consisting of only a few atomic layers. During the dropwise titration of Rhodamine 6G (R6G) solution, a longitudinal electric field was applied using a Keithley 2400 (Cleveland, OH, USA) source meter. Raman mapping revealed that under a 100 mV condition, the analyte R6G molecules were effectively confined within the pits. Due to its two-dimensional structure, MoS₂ provides a high surface area and supports a surface-enhanced Raman scattering (SERS) charge transfer mechanism. The SERS results demonstrated that the intensity in the pits of the few-layer MoS₂/patterned Si SERS substrate was approximately 274 times greater compared to planar Si, with a limit of detection reaching 10⁻⁵ M. The experimental results confirm that this method effectively resolves the issue of random distribution of analyte molecules during droplet evaporation, thereby enhancing detection sensitivity and stability. Full article

This study focused on designing an ultra-wideband metamaterial absorber, consisting of layers of Mn (manganese) and MoO₃ (molybdenum trioxide) arranged in a planar interleaving pattern, with a matrix square-shaped Ti (titanium) on the top MoO₃ layer. Key features of this research included the novel use of Mn and MoO₃ in a planar interleaving configuration for designing an ultra-wideband absorber, which was rarely explored in previous studies. MoO₃ thin film served as the fundamental material, leveraging its favorable optical properties and absorption capabilities in the infrared spectrum. Alternating layers of Mn and MoO₃ were adjusted in thickness and order to optimize absorptivity across desired wavelength ranges. Another feature is that the Mn and MoO₃ materials in the investigated absorber had a planar structure, which simplified the manufacturing of the absorber. Furthermore, the topmost layer of square-shaped Ti was strategically placed to enhance the absorber’s bandwidth and efficiency. When the investigated absorber lacked a Ti layer, its absorptivity and bandwidth significantly decreased. This structural design leveraged the optical properties of Mn, MoO₃, and Ti to significantly expand the absorption range across an ultra-wideband spectrum. When the Ti height was 280 nm, the investigated absorber exhibited a bandwidth with absorptivity greater than 0.9, spanning from the near-infrared (0.80 μm) to the mid-infrared (9.07 μm). The average absorptivity in this range was 0.950 with a maximum absorptivity of 0.989. Additionally, three absorption peaks were observed at 1010, 2510, and 6580 nm. This broad absorption capability makes it suitable for a variety of optical applications, ranging from near-infrared to mid-infrared wavelengths, including thermal imaging and optical sensing. Full article

Silicon has dimensional limitations in following Moore’s law; thus, new 2D materials complementing Silicon are being researched. Molybdenum disulfide (MoS₂) is a prospective material anticipated to bridge the gap to complement Silicon and enhance the performances of semiconductor devices and embedded systems in the package. For a synthesis process to be of any relevance to the industry. it needs to be at the wafer scale to match existing Silicon wafer-processing standards. Atomic Layer Deposition (ALD) is one of the most promising techniques for synthesizing wafer-scale monolayer MoS₂ due to its self-limiting, conformal, and low-temperature characteristics. This paper discusses the wafer-scale ALD synthesis of Molybdenum trioxide (MoO₃) using Mo (CO)₆ as a precursor with Ozone as a reactant. An ALD-synthesized wafer-scale MoO₃ thin film was later sulfurized through Chemical Vapor Deposition (CVD) to transform into stoichiometric MoS₂, which was evaluated using X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, Scanning Electron Microscopy (SEM), and Atomic Force Microscopy (AFM). The roles of activation energy and first-order reaction kinetics in determining the ALD recipe parameters of the pulse time, reactor temperature, and purge time are explicitly discussed in detail. Discretized pulsing for developing one-cycle ALD for monolayer growth is suggested. Remedial measures to overcome shortcomings observed during this research are suggested. Full article

Molybdenum trioxide (MoO₃) is an attractive semiconductor. Thus, bandgap engineering toward photoelectronic applications is appealing yet not well studied. Here, we report the incorporation of sulfur atoms into MoO₃, using sulfur powder as a source of sulfur, via a self-developed hydrothermal synthesis approach. The formation of Mo-S bonds in the MoO₃ material with the synergistic effect of sulfur doping and oxygen vacancies (designated as S-MoO_3−x) is confirmed using Fourier-transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), and electron paramagnetic resonance (EPR). The bandgap is tuned from 2.68 eV to 2.57 eV upon sulfur doping, as confirmed by UV-VIS DRS spectra. Some MoS₂ phase is identified with sulfur doping by referring to the photoluminescence (PL) spectra and electrochemical impedance spectroscopy (EIS), allowing significantly improved charge carrier separation and electron transfer efficiency. Therefore, the as-prepared S-MoO_3−x delivers a sensitive photocurrent response and splendid cycling stability. This study on the synergistic effect of sulfur doping and oxygen vacancies provides key insights into the impact of doping strategies on MoO₃ performance, paving new pathways for its optimization and development in relevant fields. Full article

This study focuses on the hole transport layer of molybdenum trioxide (MoO₃) for inverted bulk heterojunction (BHJ) organic photovoltaics (OPVs), which were fabricated using a combination of a spray coating and low-temperature annealing process as an alternative to the thermal evaporation process. To achieve a good coating quality of the sprayed film, the solvent used for solution-processed MoO₃ (S-MoO₃) should be well prepared. Isopropanol (IPA) is added to the as-prepared S-MoO₃ solution to control its concentration. MoO₃ solutions at concentrations of 5 mg/mL and 1 mg/mL were used for the spray coating process. The power conversion efficiency (PCE) depends on the concentration of the MoO₃ solution and the spray coating process parameters of the MoO₃ film, such as flow flux, spray cycles, and film thickness. The results of devices fabricated from solution-processed MoO₃ with various spray fluxes show a lower PCE than that based on thermally evaporated MoO₃ (T-MoO₃) due to a limiting FF, which gradually increases with decreasing spray cycles. The highest PCE of 2.8% can be achieved with a 1 mg/mL concentration of MoO₃ solution at the sprayed flux of 0.2 mL/min sprayed for one cycle. Additionally, S-MoO₃ demonstrates excellent stability. Even without any encapsulation, OPVs can retain 90% of their initial PCE after 1300 h in a nitrogen-filled glove box and under ambient air conditions. The stability of OPVs without any encapsulation still has 90% of its initial PCE after 1300 h in a nitrogen-filled glove box and under air conditions. The results represent an evaluation of the feasibility of solution-processed HTL, which could be employed for a large-area mass production method. Full article

This investigation focuses on the Goos–Hänchen (GH) and Imbert–Fedorov (IF) shifts on the surface of the uniaxial hyperbolic material hexagonal boron nitride (hBN) based on the biaxial hyperbolic material alpha-molybdenum (α-MoO₃) trioxide structure, where the anisotropic axis of hBN is rotated by an angle with respect to the incident plane. The surface with the highest degree of anisotropy among the two crystals is selected in order to analyze and calculate the GH- and IF-shifts of the system, and obtain the complex beam-shift spectra. The addition of α-MoO₃ substrate significantly amplified the GH shift on the system’s surface, as compared to silica substrate. With the p-polarization light incident, the GH shift can reach 381.76λ₀ at about 759.82 cm⁻¹, with the s-polarization light incident, the GH shift can reach 288.84λ₀ at about 906.88 cm⁻¹, and with the c-polarization light incident, the IF shift can reach 3.76λ₀ at about 751.94 cm⁻¹_. The adjustment of the IF shift, both positive and negative, as well as its asymmetric nature, can be achieved by manipulating the left and right circular polarization light and torsion angle. The aforementioned intriguing phenomena offer novel insights for the advancement of sensor technology and optical encoder design. Full article

Molybdenum trioxide is an abundant natural, low-cost, and environmentally friendly material that has gained considerable attention from many researchers in a variety of high-impact applications. It is an attractive inorganic oxide that has been widely studied because of its layered structure, which results in intercalation ability through tetrahedral/octahedral holes and extension channels and leads to superior charge transfer. Shape-related properties such as high specific capacities, the presence of exposed active sites on the oxygen-rich structure, and its natural tendency to oxygen vacancy that leads to a high ionic conductivity are also attractive to technological applications. Due to its chemistry with multiple valence states, high thermal and chemical stability, high reduction potential, and electrochemical activity, many studies have focused on the development of molybdenum oxide-based systems in the last few years. Thus, this article aims to briefly review the latest advances in technological applications of MoO₃ and MoO₃-based materials in gas sensors, lithium-ion batteries, and water pollution treatment using adsorption and photocatalysis techniques, presenting the most relevant and new information on heterostructures, metal doping, and non-stoichiometric MoO_3−x. Full article

Hepatitis viral infections are the most common cause of hepatitis liver disease, which eventually leads to cancer and fibrosis if not detected early. Therefore, early detection would allow for preventive and therapeutic actions. Here, a surface-enhanced Raman spectroscopy (SERS)-based biosensor was developed using plasmonic molybdenum trioxide quantum dots (MoO₃-QDs) as the SERS substrates. The nanostructured substrate of MoO₃-QDs was functionalized with a proteoglycan (syndecan-1) as a novel bioreceptor for the target hepatitis E virus (HEV). The innovative biodetection system achieved a detection limit of 1.05 fg/mL for the tested HEV target (ORF2), indicating superb clinically relevant sensitivity and performance. The designed biosensing system incorporating a glycan motif as a bioreceptor instead of the conventional antibodies or aptamers presents new insights for the ultrasensitive detection of HEV and other infectious viruses. Full article

The article describes the technology of molybdic acid recovery from spent petrochemical catalysts (HDS) developed and implemented in industrial activity. HDS catalysts contain molybdenum in the form of MoO₃ and are used for the hydrodesulfurization of petroleum products. After deactivation, due to the impurities content in the form of sulfur, carbon and heavy metals, they constitute hazardous waste and, at the same time, a valuable source of the Mo element, recognized as a critical raw material. The presented technology allows the recovery of molybdic acid with a yield of min. 81%, and the product contains min. 95% H₂MoO₄. The technology consisted of oxidizing roasting of the spent catalyst, then leaching molybdenum trioxide with aqueous NaOH to produce water-soluble sodium molybdate (Na₂MoO₄), and finally precipitation of molybdenum using aqueous HCl, as molybdic acid (H₂MoO₄). Industrial-scale testing proved that the technology could recover Mo from the catalyst and convert it into marketable molybdic acid. This proves that the technology can be effectively used to preserve molybdenum. Full article