UV-visible Reflectance Spectroscopy Research Articles

Solar driven highly efficient photocatalyst based on Dy2O3 nanorods deposited on reduced graphene oxide nanocomposite for methylene blue dye degradation.

In recent years, the demand for rare earth elements has surged due to their unique characteristics and diverse applications. This investigation focuses on utilizing the rare earth element dysprosium oxide (Dy2O3) for the photocatalytic oxidation of model pollutants under solar light irradiation. A novel RGO-Dy2O3 nanocomposite photocatalyst was developed using a solvothermal approach, Dy2O3 nanorods uniformly deposited onto reduced graphene oxide (RGO) nanosheets. Comprehensive characterization techniques, including Brunner-Emmett-Teller (BET), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), Fourier transform-infrared spectroscopy (FTIR), Raman spectroscopy, high resolution - transmittance electron microscopy (HR-TEM), field emission-electron scanning microscopy (FE-SEM), atomic force microscopy (AFM), electron paramagnetic resonance spectroscopy (EPR), photoluminescence spectroscopy (PL), and electrochemical impedance spectroscopy EIS techniques. The UV-visible diffusive reflectance spectroscopy (UV-Vis-DRS) studies revealed a band gap energy of 3.18eV and a specific surface area of 114 m2/g for the fabricated RGO-Dy2O3 nanocomposite. The RGO-Dy2O3 nanocomposite demonstrated a high photocatalytic degradation efficiency of 98.1% at neutral pH for methylene blue (MB) dye for the dye concentration of 10ppm. The remarkable photocatalytic performance was achieved within 60min under solar light irradiation. Reusability tests demonstrated stability, maintaining over 90% photocatalytic efficiency after three cycles. The EPR spectra and quenching experiments confirmed that photogenerated hydroxyl radicals significantly influence the photodegradation processes. The RGO-Dy2O3 nanocomposite photocatalyst, with its green, easy preparation process and recycling capabilities, presents an ideal choice for various applications. It offers a viable alternative for the photocatalytic degradation of organic dyes in real wastewater, contributing to sustainable environmental remediation.

A novel barium zirconate titanate/Fe-MOF nanocomposite: Synthesis, characterization, and photocatalytic mechanism

The synthesis of a metal-organic framework (MOF) matrix of MIL-100 (Fe) loaded with BaTi0.85Zr0.15O3 (BTZ) nanoparticles (NPs) was achieved by an easy one-pot solvothermal procedure and encasing of BTZ NPs. X-ray diffraction (XRD), photoluminescence spectroscopy (PL), UV-Vis reflectance spectroscopy (DRS), Transmission electron microscopy (TEM), scanning electron microscopy (SEM), and N2 adsorption-desorption were deployed for the characterization of the synthesized samples. The degradation efficiency for tetracycline (TC), among the photocatalytic BTZ/MIL-100(Fe) nanocomposites with varied BTZ percentages (10, 20, 30, and 40 wt% BTZ), revealed that (30 wt%), offered the best outcome. At 0.8 g L-1 of the catalyst, pH 9, 30 ppm TC solution, and 180 min irradiation time, as the optimal conditions, the degradation efficiency of TC molecules reached >90. Based on the study of some scavenging agents, the importance of the reactive species in TC photodegradation followed the trend of photogenerated e-, hydroxyl radicals, superoxide radicals, and photogenerated h+. TC degradation occurred through reduction and oxidation pathways via a direct Z-scheme mechanism. This work aims to describe the use of MOF-based materials as a visible-light-driven photocatalyst towards TC.

Encapsulation of the vanadium substituted Keggin polyoxometalates [α-PVW11O40]4- and [α-PV2W10O40]5- in HKUST-1.

Two POM@MOF hybrid materials composed of a copper-based metal-organic framework (MOF) [Cu3(C9H3O6)2(H2O)3]n (HKUST-1) encapsulating vanadium-substituted Keggin polyoxometalates (POM), [α-PVW11O40]4- (PVW11) and [α-PV2W10O40]5- (PV2W10), were prepared and characterized. PVW11@HKUST-1 and PV2W10@HKUST-1 were synthesized hydrothermally by self-assembly of HKUST-1 in the presence of the preformed POMs, [α-PVW11O40]4- and [α-PV2W10O40]5-, respectively. The two POM@MOF composites were characterized by X-ray diffraction, TGA, BET surface area analysis and FT-IR and Raman spectroscopy. The electronic structure of the POM@MOF materials and their respective constituents is surveyed using solid state UV-vis reflectance spectroscopy. The UV-vis spectra order the oxidizing strength of the POM constituents ([α-PV2W10O40]5- > [α-PVW11O40]4-) and reveal the distinct electronic structure of the POM@MOF materials obtained by synthetic encapsulation of mono- and di-vanadium substituted Keggin polyoxotungstates in HKUST-1.

Anodization of cast and sintered Fe40Al alloy in etidronic acid: Morphological and semiconductive properties of the oxide films

Fe40Al alloys produced by casting and sintering were anodized to form nanostructured oxide layers. Microstructural characterization revealed a lower grain size for the sintered alloy compared to the cast alloy. Anodizing was performed in four electrolytes with a constant etidronic acid concentration (0.3 M) and different ethylene glycol-water ratios. Different voltages (5–400 V) and treatment times (1–4 hours) were evaluated for cast and sintered Fe40Al alloys. Among the studied anodization regimes, only four anodic films formed on sintered Fe40Al were homogeneous. These films were annealed at 900°C and analyzed by conventional characterization techniques (SEM/EDS and XRD). Results indicated a non-self-ordered morphology and different content of P, Fe, and Al species as a function of the electrolyte composition. Annealing post-treatment led to the formation of Fe/Al oxides and spinels in selected anodic films. An additional peak of FePO4 was detected only in the anodic film formed in pure ethylene glycol. The band gap values (UV-Vis reflectance spectroscopy) of the anodic film formed in ethylene glycol decreased from 2.87 eV to 2.45 eV after annealing. This band gap decrease was associated with the preferential formation of conductive phases (Fe2O3 and FeAlO3) over insulating phases (γ-Al2O3 and FeAl2O4) after annealing.

Ag–CdS-Coated Cladding-Modified Fiber-Optic Sensor for Detection of NO2 Gas

In this study, a cladding-modified fiber-optic sensor is reported for NO2 gas detection. Monitoring the purity of air is the need of the hour, with the growing technologies. Hence, in this work, Ag-doped CdS is coated over the cladding-removed region of 3[Formula: see text]cm length by Chemical Bath Deposition (CBD) which acts as the gas-sensing medium. Ag–CdS is coated over four fibers each with a different coating duration of 10[Formula: see text]min, 20[Formula: see text]min, 30[Formula: see text]min and 40[Formula: see text]min. Characterization of Ag–CdS is done by Scanning Electron Microscope (SEM), UV-visible absorption spectroscopy and UV-visible reflectance spectroscopy. The spectral response for different concentrations of NO2 is studied on the four fibers separately, and it is analyzed and compared. The minimum detection limit is 100[Formula: see text]ppm and the response time is 10[Formula: see text]min. Out of the four fibers, Ag–CdS-30 exhibited the best response with a sensitivity of 15.5%. The results are compared with cladding-modified fiber coated with CdS, which was reported previously. The effect of Ag-doping is analyzed.

Tailoring structural and optical properties of Cu(II)-induced MgAl2O4 nanoparticles and their response to toxic dyes under solar illumination.

Worldwide environmental challenges pose critical problems with the growth of the global economy. Addressing these issues requires the development of an eco-friendly and sustainable catalyst for degrading organic dye pollutants. In this study, copper-doped magnesium aluminates (CuxMg1-xAl2O4) with x = 0.0-0.8 were synthesized using a citrate-based combustion route. The inclusion of Cu(II) significantly impacted the structural, microstructural, optical, and photocatalytic activity of the catalyst. Rietveld analysis of X-ray diffraction powder profiles revealed single-phase spinels crystallized in the face-centered cubic unit cell with space group. Chemical states of the ions, surface morphology, and elemental investigation were analyzed by X-ray photoelectron spectroscopy, field-emission scanning electron microscopy, and energy-dispersive X-ray spectroscopy, respectively. UV-visible and diffuse reflectance spectroscopies confirmed the reduction of the band gap due to Cu(II) doping, validated by first-principle investigations using the WIEN2k code. The catalyst with x = 0.8 showed higher photocatalytic efficacy (90% and 93%) for removing two azo organic dye pollutants, rhodamine B and methyl orange, respectively, within 120min. Degradation kinetics followed a pseudo-first-order mechanism. The doped (0.8) sample was structurally and morphologically stable and reusable under visible irradiation, retaining performance after three runs. Scavenger studies confirmed hydroxyl and superoxide radicals' involvement in the degradation. This work presents an effective approach to enhancing CuxMg1-xAl2O4 catalysts' photodegradation performance, with potential applications in pharmaceuticals and wastewater remediation.

Phase transitions in NiO during the oxygen evolution reaction assessed via electrochromic phenomena through operando UV–Vis spectroscopy

Due to its high activity and stability, nickel oxide (NiO) has shown significant promise as an electrocatalyst for the alkaline oxygen evolution reaction (OER). In parallel, NiO exhibits a well-known electrochromic phenomenon, changing its optical properties in response to an applied electric potential. This study investigates the relationship between NiO phase changes that occur during the OER and the connected optical modulation using operando UV–visible reflectance spectroscopy. The correlation between the OER activity and the electrochromic behavior of NiO is explored, providing insights into the underlying physicochemical mechanisms governing both phenomena. Strong reduction of the reflected light at higher applied potentials cannot be attributed solely to the change in optical bandgap due to the phase change or the change in the material's refractive index when different phases form. Therefore, in-gap states responsible for increasing the absorption at higher applied potentials were experimentally characterized by ultraviolet photoelectron spectroscopy (UPS) and X-ray absorption spectroscopy (XAS). The results show that phase changes in NiO during OER influence its optical absorption characteristics, which in turn give access to following active phase changes of the electrocatalyst material through a non-invasive, optical, operando probe in real time allowing for kinetic studies of the involved solid-state conversion reactions.

XPS valence band observable light-responsive system for photocatalytic acid Red114 dye decomposition using a ZnO–Cu2O heterojunction

ZnO–Cu2O composites were made as photocatalysts in a range of different amounts using an easy, cheap, and environment-friendly coprecipitation method due to their superior visible light activity to remove pollutants from the surrounding atmosphere. X-ray diffraction and Fourier transform infrared spectroscopy (FT-IR) have demonstrated that ZnO–Cu2O catalysts are made of highly pure hexagonal ZnO and cubic Cu2O. X-ray photoelectron spectroscopy has confirmed that there is a substantial interaction between the two phases of the resultant catalyst. The optical characterizations of the synthesized ZnO–Cu2O composite were done via UV–vis reflectance spectroscopy. Due to the doping on ZnO, the absorption range of the ZnO–Cu2O catalyst is shifted from the ultraviolet to the visible region due to diffuse reflection. The degradation efficiency is affected by the Ratio of ZnO: Cu2O and ZnO–Cu2O composite with a proportion of 90:10 exhibited the most prominent photocatalytic activity on Acid Red 114, with a pseudo-first-order rate constant of 0.05032 min−1 that was 6 and 11 times greater than those of ZnO and Cu2O, respectively. The maximum degradation efficiency is 97 %. The enhanced photocatalytic activity of the composite is caused by the synergistic interaction of ZnO and Cu2O, which improves visible light absorption by lowering band gap energy and decreasing the rate at which the electron-hole pairs recombine. The scavenging experiment confirmed that hydroxyl radical was the dominant species for the photodegradation of Acid Red 114. Notably, the recycling test demonstrated the ZnO–Cu2O photocatalyst was highly stable and recyclable. These results suggest that the ZnO–Cu2O mix might be able to clean up environmental pollutants when it meets visible light.

Not all apparently gynandromorphic butterflies are gynandrous: The case of Polyommatus icarus and its relatives (Lepidoptera: Lycaenidae)

Beside the more than two thousand normal specimens of Polyommatus icarus (Rottemburg, 1775) yielded by rearing experiments, there was one perfectly bilateral dichromatic individual first considered to be gynandrous. On the basis of analysing genitalia traits, wing surface covering scale micromorphology, and the spectral characteristics of the blue colour generated by the cover scales, the gender of the specimen has been identified as female. This exemplar was investigated in comparison with gynandrous specimens from the collections of the Hungarian Natural History Museum exhibiting various degrees of intermixing of blue and brown coloration. Focus stacking microscopy for detailed scale morphology and UV–visible reflectance spectroscopy was used for the characterization of the optical properties. Inspecting literature references and the Lycaenidae collection of the museum, further examples have been found for female bilateral dichromatism in the closely related polyommatine lycaenid species Lysandra bellargus (Rottemburg, 1775) and Lysandra coridon (Poda, 1761) what suggests that polyommatine female dichromaticity may be displayed by the manner of bilaterality and mosaicism, phenomena hitherto solely connected to gynandromorphy.

Preparation of high color fastness structural colored cotton fabric via SiO2@PDA photonic crystal

Structural color is an important way to achieve the ecological coloring of textiles. SiO2 microspheres with sizes in the range of 200–337 nm were synthesized by the Stober method and then covered with highly light-absorbing melanin PDA to form SiO2@PDA photonic crystals. The SiO2@PDA photonic crystals were assembled onto the surface of white cotton fabrics by gravity deposition to achieve structural color. The addition of polyvinylpyrrolidone (PVP) enhances interfacial bonding by forming multiple hydrogen bonds between its lactam group and the phenolic hydroxyl group of PDA, resulting in a structured color cotton fabric with high color fastness. Scanning electron microscopy (SEM) was used to study the structure and morphology of SiO2@PDA microspheres. The chemical compositions of PDA and PVP were surveyed by Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD). The surface structural color of cotton fabrics was investigated by UV–Vis reflectance spectroscopy.

High performance Co3O4/Sn-ZnO nanocomposite photocatalyst for removal of methylene blue dye

Methylene blue is a toxic, carcinogenic, and non-biodegradable synthetic dye discharged from factories and industries that causes severe harm to human health and environmental pollution. Therefore, in this work, Co3O4/Sn-ZnO nanocomposite was synthesized using a simple sol–gel method for efficient photocatalytic removal of methylene blue dye in an aqueous basic medium. The structural, optical, photoluminescence, morphological, and compositional properties were studied. The XRD result revealed that the crystal size increases as the full width at half maxima (FWHM) decreases when Co3O4 are coupled with Sn-ZnO. From UV-visible diffusive reflectance and photoluminescence spectroscopies, a narrowing of the band gap and a reduction of the charge carrier’s recombination rate were observed, respectively. The photocatalytic efficiency and degradation rate constant of 95.1% and 0.03251 min−1 were recorded for methylene blue dye upon the use of optimized catalyst dosage of 60 mg Co3O4/Sn-ZnO nanocomposite catalyst under an irradiation time of 100 min at room temperature for optimized pH value of 9 in an aqueous basic medium.

Immobilization of Bi2WO6 on Polymer Membranes for Photocatalytic Removal of Micropollutants from Water - A Stable and Visible Light Active Alternative.

In this work, bismuth tungstate Bi2WO6 is immobilized on polymer membranes to photocatalytically remove micropollutants from water as an alternative to titanium dioxide TiO2. A synthesis method for Bi2WO6 preparation and its immobilization on a polymer membrane is developed. Bi2WO6 is characterized using X-ray diffraction and UV-vis reflectance spectroscopy, while the membrane undergoes analysis through scanning electron microscopy, X-ray photoelectron spectroscopy, and degradation experiments. The density of states calculations for TiO2 and Bi2WO6, along with PVDF reactions with potential reactive species, are investigated by density functional theory. The generation of hydroxyl radicals OH• is investigated via the reaction of coumarin to umbelliferone via fluorescence probe detection and electron paramagnetic resonance. Increasing reactant concentration enhances Bi2WO6 crystallinity. Under UV light at pH 7 and 11, the Bi2WO6 membrane completely degrades propranolol in 3 and 1 h, respectively, remaining stable and reusable for over 10 cycles (30 h). Active under visible light with a bandgap of 2.91eV, the Bi2WO6 membrane demonstrates superior stability compared to a TiO2 membrane during a 7-day exposure to UV light as Bi2WO6 does not generate OH• radicals. The Bi2WO6 membrane is an alternative for water pollutant degradation due to its visible light activity and long-term stability.

Synthetization and Characterization of Zinc Oxide Nanoparticles by X- Ray Diffractometry (XRD), Fourier Transforms, Infra-Red Spectroscopy (FT-IR), Scanning Electron Microscopy (SEM) and Antibacterial Activity Test

Purpose: Nanomaterials with their derivable potentials offer wide obtain ability and have recently aroused much attention for biomedical applications. Nowadays, nanomaterials-based colorimetric sensing is a quickly emerging field of sensing applications. Nanomaterials are considered as the main component of colorimetric determination of hydrogen peroxide to replace the natural enzyme-based sensors because of some associated intrinsic drawbacks. Considering the advantageous properties of ionic liquid (IL) for various applications, significant attention has been made to the use of ionic liquid stabilized metal NPs which may serve as a regulator to enhance the catalytic performance of the metal nanoparticles in the different IL reaction medium. 
 Methodology: The peroxidase-like activity of IL coated metal NPs (IL-MNPs) have been considered for the catalytic oxidation reaction of chromogenic substrate 3,3,5,5- tetramethylbenzidine (TMB) in the presence of H2O2 at an estimated wavelength of 652 nm.
 Results: The synthesized metal nanoparticles (Ag) were produced using a chemical reduction method. Various characterization techniques like FTIR, UV-Visible spread Reflectance Spectroscopy [UV-VIS DRS], were employed, which verified the structure, nano-size and successful combination of metal dopant ion into the samples. The molecular structure of ionic liquid with varying cations was produced and confirmed by 1H-NMR spectroscopy. The ionic liquid was coated on metal nanoparticles to enhance their conductivity. 
 Unique Contribution to Theory, Practice and Policy: Optimized reaction conditions like pH, temperature and catalyst dosage affect catalytic activity and color sensing properties. The coating of [Min] Ac on Ag achieved low detection limits and colorimetric detection of [Pyr] based Ag.

Assembling ZnMnFe2O4@Ag-AgVO3 nanostructure heterojunctions for photocatalytically degrading RhB and Pseudomonas aeruginosa bacteria under visible irradiation

Improving the separation of photocarriers is a vital approach to create highly effective heterojunction photocatalysts for the photodegradation of environmental pollutants. In this work, coprecipitation and hydrothermal methods were employed to develop a new heterojunction of Zn0.5Mn0.5Fe2O4@Ag-AgVO3 magnetic nanocomposite as photocatalysts for the photodegradation of Rhodamine B (RhB) and bacterial inactivation of Pseudomonas aeruginosa (P. aeruginosa) when exposed to illumination of visible light. FESEM, EDX, UV–vis reflectance spectroscopy (DRS), N2 adsorption/desorption, TEM, PL, Brunauer-Emmett-Teller (BET) surface area, Vibrating Sample Magnetometer (VSM), and XRD techniques were used to investigate the structural and optical properties of synthesized materials. The Zn0.5Mn0.5Fe2O4@Ag-AgVO3 photocatalyst demonstrated noticeably higher photocatalytic activity for RhB degradation when compared to the pure constituents AgVO3, Ag-AgVO3, and Zn0.5Mn0.5Fe2O4 samples. The results revealed that when RhB was used at a concentration of 20 ppm, the Zn0.5Mn0.5Fe2O4@Ag-AgVO3 possessed a high degradation rate (93.43 % within 180 min), and this was sufficient to get the highest total organic carbons (TOC) removal (90 %). Besides, Zn0.5Mn0.5Fe2O4@Ag-AgVO3 possesses complete inactivation efficiency (log(CFU) decreased from 6.5 to 0.00001) toward P. aeruginosa in 120 min of visible illumination. The photodegradation mechanism was explained by the surface plasmonic resonance Z-type heterostructure, and tested by trapping experiments. It can beinferredthat the Zn0.5Mn0.5Fe2O4@Ag-AgVO3 photocatalyst was very stable and efficient in removing different organic pollutants and pathogenic bacteria from wastewater.

Efficient sunlight-assisted degradation of organic dyes using V2O3/g-C3N4 nanocomposite catalyst

This study reports the synthesis of vanadium oxide (V2O3) and graphitic carbon nitride (g-C3N4) nanocomposite for simple sunlight-assisted degradation of Methylene Blue(MB) and Rhodamine B (RhB) dyes. Herein, the V2O3 and g-C3N4 are synthesized via hydrothermal and thermal decomposition techniques, respectively. X-ray diffraction (XRD) analysis confirms the formation of the rhombohedral and hexagonal structures of V2O3 and g-C3N4 in the nanocomposite, respectively, while scanning electron microscopy (SEM) reveals the sheet-like morphology of g-C3N4 and V2O3 nanoparticles. The optical band gap of the nanocomposite is estimated as 1.89 eV using a Tauc's plot generated from UV–Vis reflectance spectroscopy. The as-synthesized nanocomposite exhibits an excellent dye degradation efficacy displaying a 100 % degradation of RhB and 90 % degradation of MB dyes within 1 h of exposure to daylight. This performance is attributed to the synergistic effect of the V2O3/g-C3N4 nanocomposite wherein the composite benefits from the large surface area and high visible light adsorption of g-C3N4, combined with the active catalytic sites of the rhombohedral V2O3 structure, resulting in its high efficiency for photocatalytic dye degradation. Scavenger studies confirm the hydroxyl (.OH) radicals and oxygen (O2−.) radicals as the primary reactive species in the degradation process MB. Furthermore, the catalyst exhibited remarkable stability over three cycles of photocatalysis thus confirming its utility for real-time environmental remediation applications.

Mixed Nanosphere Assemblies at a Liquid-Liquid Interface.

The in-plane packing of gold (Au), polystyrene (PS), and silica (SiO2) spherical nanoparticle (NP) mixtures at a water-oil interface is investigated in situ by UV-vis reflection spectroscopy. All NPs are functionalized with carboxylic acid such that they strongly interact with amine-functionalized ligands dissolved in an immiscible oil phase at the fluid interface. This interaction markedly increases the binding energy of these nanoparticle surfactants (NPSs). The separation distance between the Au NPSs and Au surface coverage are measured by the maximum plasmonic wavelength (λmax) and integrated intensities as the assemblies saturate for different concentrations of non-plasmonic (PS/SiO2) NPs. As the PS/SiO2 content increases, the time to reach intimate Au NP contact also increases, resulting from their hindered mobility. λmax changes within the first few minutes of adsorption due to weak attractive inter-NP forces. Additionally, a sharper peak in the reflection spectrum at NP saturation reveals tighter Au NP packing for assemblies with intermediate non-plasmonic NP content. Grazing incidence small angle X-ray scattering (GISAXS) and scanning electron microscopy (SEM) measurements confirm a decrease in Au NP domain size for mixtures with larger non-plasmonic NP content. The results demonstrate a simple means to probe interfacial phase separation behavior using in situ spectroscopy as interfacial structures densify into jammed, phase-separated NP films.

Structural transition and magnetization reversal in rare earth doped R0.5Sr0.5Fe0.5Cr0.5O3 (R[dbnd]La, Nd and Sm) perovskite oxides containing mixed valent cations at B site: Magnetic, optical and transport properties

In the current paper, the effect of lanthanide metal cation substitution on structural, magnetic, optical and transport properties of R0.5Sr0.5Fe0.5Cr0.5O3 (RLa, Nd and Sm) perovskite oxides have been investigated. Structural investigations reveal that there is a phase transition from cubic to orthorhombic symmetry with the doping of heavier rare earth ion. The findings of XPS studies point to the existence of mixed valence states of Cr and Fe ions. The change in magnetization in response to an external magnetic field reveals that the phases have a mostly antiferromagnetic character with some trace amounts of ferromagnetic components. In temperature dependent magnetization studies, magnetic reversal has been observed in Nd doped sample, while La and Sm doped samples only show positive magnetization. The band gap energies of the synthesized materials determined from the UV–vis reflectance spectroscopy lie in the range of 1.60–1.78 eV indicating the semi-conducting nature of the samples. The temperature-dependent resistivity measurements show semi-conducting behaviour of the samples with decreasing temperature which finally become insulating at low temperature. It has been shown that the VRH model provides the best fit for the resistivity data when compared to the other transport mechanism models that were used to describe the electrical conduction process of synthesized phases.

High-Selectivity Hydrogen Gas Sensors based on Mesoporous PbOx-ZnO Nanocomposites.

Hydrogen heralded as a promising renewable and environmentally friendly energy carrier, carries inherent risks owing to its highly flammable nature. A mere 4 % concentration of hydrogen in the air can trigger an explosion. To counteract this peril, a composite material comprising PbOX-ZnO (2 : 1) was synthesized, characterized, and subsequently employed to fabricate a hydrogen sensing device. Various analytical tools were used to characterize as-deposited materials, including X-ray diffraction, Scanning electron microscopy /Energy Dispersive X-ray Spectroscopy, Transmission electron microscopy UV-Vis Reflectance Spectroscopy and Fourier-transform infrared spectroscopy. The device exhibited favorable properties, such as good selectivity, stability, and a low detection limit for hydrogen. At ambient room temperature, the device demonstrated a sensing signal reaching 468.7, with a response time (T90) of 155 seconds and a recovery time (Tr90) of 69 seconds when exposed to a hydrogen concentration of 5 ppm. This performance underscores the device's rapid and effective response to hydrogen exposure. Moreover, the PbOX-ZnO (2 : 1) composite-based device exhibited a detection limit of 2.4 ppm, functioning accurately within a linear range spanning from 5 ppm to 50 ppm. This capability confirms its precision in accurately detecting hydrogen concentrations within this designated range.

Compositional Influence of Synthesized Magnetic Nanoparticles on Epoxy Composites: Dielectric, Magnetic, and Optical Characteristics

Epoxy nano-magnetic composites exhibit remarkable and promising properties by synergistically combining the properties of epoxy resin and magnetic nanofillers. The current study deals with the synthesis of Fe3O4, NiFe2O4, and CoFe2O4 nanoparticles and their respective nanoparticles-doped epoxy composites, as well as the structural, optical, and dielectric characterization of the resultant nano-composites. To investigate the surface morphology of the synthesized nanoparticles, field emission electron microscopy (FESEM) analysis was employed. By measuring electron diffraction spectroscopy (EDS), the presence of various chemicals was verified. X-ray diffraction (XRD) was used to determine the structural details of the synthesized nanoparticles and nanoparticles-doped epoxy composites. The structural chemistry and surface functionality of the nano-epoxy composites were investigated using Fourier transform infrared spectroscopy (FTIR). The magnetic properties of the synthesized nanoparticles and nanoparticles loaded epoxy composites were also studied using a vibrating sample magnetometer (VSM). UV–visible reflection spectroscopy was also carried out to find the optical properties of the synthesized nanoparticles, neat (undoped) epoxy, and nanoparticles-doped epoxy composites. Dielectric spectroscopy measurements of nanoparticles-doped epoxy composites were performed using an Agilent E4980A precision LCR (Inductance Capacitance Resistance) meter with an Agilent 16451B-test fixture LCR and vector network analyzer (VNA) in the frequency span of 10 kHz to 2 MHz and 200 MHz to 20 GHz, respectively. The influence of the synthesized nanoparticles on the neat (undoped) epoxy composites and the results in view of future applications are fully discussed.

Morphological and semiconductive properties of the anodic oxide layers made on Fe3Al alloy by anodizing in tartaric-sulfuric acid mixture

It has recently been found that the anodizing of FeAl alloys allows the formation of iron-aluminum oxide layers with interesting semiconducting properties. However, the lack of systematic research on different anodizing regimes is hampering their full exploitation in numerous photoelectrochemical-related applications. This study address, for the first time, the systematic effect of the electrolyte composition on the formation of self-ordered oxide films by anodizing on cast Fe3Al alloy. The Fe3Al alloy was anodized in 3 electrolytes with different water-ethylene glycol (EG) ratios (pure water, 25 vol.%-EG, and 50 vol.%-EG solutions) at a constant tartaric-sulfuric acids concentration, different voltages (10–20 V) and treatment times (2–60 min). After anodizing, all anodic oxide layers were annealed at 900 °C to form semiconductive iron-aluminum crystalline phases. Conventional techniques were used to systematically ascertain the morphological (SEM/EDS, XRD, eddy-current measurements) and semiconductive (UV–VIS reflectance spectroscopy) properties of these oxide layers. The results confirmed the formation of homogeneous and self-ordered anodic oxide layers at 10 and 15 V, regardless of the electrolyte composition. Namely, anodic films formed in electrolytes containing EG showed lower pore sizes, growth rates, and film thicknesses than those anodic films formed in the aqueous-based electrolyte. The annealing post-treatment results in different Fe-Al oxides (FexOy, FeAl2O4, etc.) with superior band gap values than those for non-annealed films.