Energy Dispersive Spectroscopy Research Articles

Characterization of GaAs and GaAs/Cr/GaAs interfacial layers fabricated via magnetron sputtering on silicon (100)

The obtaining and study of semiconductor materials have been topics of interest for decades. However, alternatives that allow greater versatility at the time of their application have yet to be explored, such as the inclusion of some transition metals. In this work, we report the obtaining of GaAs and GaAs/Cr/GaAs layers, which were prepared by r.f. magnetron sputtering on a Si (100) substrate by varying the deposition time of the intermediate Cr layer for t = 5 min and 10 min, respectively. Scanning electron microscopy in cross-section was carried out to determine the growth mode of the GaAs and GaAs/Cr/GaAs films. The percentage of the elements in the GaAs/Cr/GaAs thin films was determined through energy dispersive spectroscopy (EDS) in cross-sections along the entire layer thickness. X-ray diffraction and micro-Raman spectroscopy at room temperature were measured to analyze the formation of CrAs and GaCr binary phases by diffusion across interlayers. Finally, we conclude on the possible use of this technique to obtain semiconductor alloys with Cr inclusion.

Corrosion effects of Na2CO3/NaCl molten salt eutectic on 316L stainless steel under isothermal and cycling conditions

Using phase-change materials in thermal energy storage systems for concentrating solar thermal plants can significantly reduce the volume of storage media and, therefore, the cost of the system. However, this approach introduces new material compatibility issues between the thermal energy storage material and the containment vessel in the form of corrosion and thermal transients, which are inherent in these systems. Rods and sheet coupons of stainless steel 316L were corroded for up to 768 h in 59.4/40.6 wt% Na2CO3/NaCl eutectic salt under isothermal (650 °C) and cycled conditions (between 600 and 650 °C). The testing methodologies correspond to actual service conditions, as isothermal degradation may not represent material loss under typical solar thermal cycling conditions. Mass losses were calculated via the Dynamic Gravimetric Analysis technique while Scanning Electron Microscopy utilizing Energy Dispersive Spectroscopy was used to analyze the corrosion layers. Isothermal mass loss plateaued at 75 mg/cm2 at 96 h with no further measurable loss after this time, while cycled samples had a fast initial mass loss rate of 60 mg/cm2 in the first 96 h and lost 0.0331 mg/cm2 every hour thereafter. The results indicate that isothermal samples corrode more slowly than the predominant industry cases of thermal cycling. Spalling is responsible for the degradation in both sets; the continual temperature changes in the cycled samples lead to additional stresses, exacerbating the effect.

Enhanced adsorption and removal of Cd(II) from aqueous solution by amino-functionalized ZIF-8

Zeolite imidazolate framework-8 (ZIF-8), which is a special subgroup of metal–organic frameworks (MOFs), was synthesized and modified by ethylenediamine (ZIF-8-EDA) to prepare an efficient adsorbent for the high sorption of Cd2+ ions from solution. The synthesized and modified ZIF-8 (ZIF-8-EDA) were characterized by X-ray diffraction (XRD), Fourier-transform infrared (FT-IR) spectroscopy, Brunauer–Emmett–Teller (BET), field emission scanning electron microscopy (FE-SEM) with energy dispersive spectroscopy (EDS), and transmission electron microscopy (TEM) analysis. The optimum conditions for dosage of adsorbent, initial ion concentration, pH, and contact time were 0.05 g/l, 50 mg/l, 6, and 60 min, respectively, for cadmium ion sorption from aqueous solutions with a removal efficiency of 89.7% for ZIF-8 and 93.5% for ZIF-8-EDA. Adsorption kinetics and equilibrium data were analyzed using the Langmuir and Freundlich equations. The Langmuir model fitted the equilibrium data better than the Freundlich model. According to the Langmuir equation, the maximum uptake for the cadmium ions was 294.11(mg/g). The calculated thermodynamic parameters (ΔG°, ΔH°, and ΔS°) indicated that the adsorption process was feasible, spontaneous, and endothermic at 20–50 °C. Based on the results, the amino functionalized ZIF-8 had improved adsorption performance due to the replacing of the starting linker with organic ligands that had effective functional groups, leading to chemical coordination due to the interaction of metal ions with the non-bonding pair of electrons on the N atoms of the amino functional group. The selectivity toward metal ion adsorption by ZIF-8-EDA was Cd2+ > Pb2+ > Ni2+‏.

Reduction of an Ilmenite Concentrate by Using a Novel CO2/CH4 Thermal Plasma Torch

Plasma technology has emerged as a very helpful tool in a variety of sectors, notably metallurgy. Innovators and scientists are focused on the problem of finding a more ecologically friendly way of extracting titanium and iron metal from natural ilmenite concentrate for industrial applications. A direct current (DC) plasma torch operating at atmospheric pressure is used in this study to describe a decarbonization process for reducing an ilmenite concentrate. The plasma gases employed in this torch are CO2 and CH4. The molar ratio of the gases may be crucial for achieving a satisfactory reduction of the ilmenite concentrate. As a result, two molar ratios for CO2/CH4 have been chosen: 1:1 and 2:1. During torch operation, a thin layer of graphite is formed on the cathode to establish a protective barrier, prolonging the cathode’s life. The material was analyzed using X-ray diffraction (XRD) and scanning electron microscopy with energy dispersive spectroscopy (SEM-EDS). The output gases were analyzed using mass spectrometry (MS). In addition, a thermodynamic analysis was performed to predict the development of thermodynamically stable phases. An economic assessment (including capital expenditures (CAPEX) and operating expenditures (OPEX)) and a carbon balance were developed with the feasibility of the piloting in mind.

One‐step synthesis of a spongy flexible substrate for surface enhanced Raman spectroscopy comprising a silver nanoparticles‐loaded poly(amidoamine) dendrimer crosslinked with glutaraldehyde

AbstractA composite comprising a silver nanoparticles‐loaded poly(amidoamine) (PAMAM) dendrimer crosslinked with glutaraldehyde (PAMAM/AgNPs) is synthesized using a one‐step method under vortex at room temperature. The structure of glutaraldehyde‐crosslinked PAMAM dendrimer is characterized using FTIR and high‐resolution magic angle spinning–carbon 13 nuclear magnetic resonance (HRMAS 13C NMR) spectroscopy. The crosslinking structure ensures the uniformity and stability of the Ag nanoparticles, and the flexibility of the PAMAM/AgNPs composite. X‐ray diffraction (XRD) analysis and energy dispersive spectroscopy (EDS) confirm the formation of Ag nanoparticles in the PAMAM/AgNPs composite. Scanning electron microscopy (SEM) and three‐dimensional (3D) micro‐Raman images reveal the coarsely porous 3D micro‐structure of the PAMAM/AgNPs composite. This unique micro‐3D architecture provides the PAMAM/AgNPs composite with spongy flexibility and a swab‐like nature, which is advantageous for the rapid and effective absorption of liquid samples on the surfaces of objects. Surface enhanced Raman spectroscopy (SERS) indicates that the detection limits of both rhodamine 6G (R6G) and thiram are 1.0 × 10−5 mol L−1, and the SERS enhancement factor of R6G is determined to be 1.35 × 104. The spongy flexible PAMAM/AgNPs SERS substrate therefore has potential for use in Raman active compound detection.

Study of Nanohydroxyapatite Coatings Prepared by the Electrophoretic Deposition Method at Various Voltage and Time Parameters

The aim of the work is to compare the properties of nanohydroxyapatite coatings obtained using the electrophoretic deposition method (EDP) at 10 V, 20 V, and 30 V, and with deposit times of 2 and 5 min. The primary sedimentation was used to minimize the risk of the formation of particle agglomerates on the sample surface. Evaluation of the coating was performed by using a Scanning Electron Microscope (SEM), Energy-Dispersive Spectroscopy (EDS), Atomic Force Microscopy (AFM), optical profilometer, drop shape analyzer, and a nanoscratch tester. All of the coatings are homogeneous without any agglomerates. When low voltage (10 V) was used, the coatings were uniform and continuous regardless of the deposition time. The increase in voltage resulted in the formation of cracks in the coatings. The wettability test shows the hydrophilic behavior of the coatings and the mean contact angle values are in the range of 20–37°. The coatings showed excellent adhesion to the substrate. The application of a maximum force of 400 mN did not cause delamination in most coatings. It is concluded that the optimal coating for orthopedic implants (such as hip joint implants, knee joint implants or facial elements) is obtained at 10 V and 5 min because of its homogeneity, and a contact angle that promotes osseointegration and great adhesion to the substrate.

Improved Electrocatalytic Degradation of Alizarin Yellow R by Ti/Zr-SnO2/PbO2 Electrodes Doped with Ytterbium

Introduction: Electrochemical oxidation of Alizarin Yellow R (AYR) was investigated on Ytterbium (Yb) doped Ti/PbO2 electrodes prepared by an electrodeposition method. Method: The etching of the Ti sheet by using a mixed acid of H2SO4 and TA (volume ratio= 2: 1) for 50 min at 100 °C could produce a suitable interface for further modification. The morphologies, composition, and electrochemical properties of Yb doping on the electrode were characterized by SEM (Scanning Electron Microscopy), EDS (Energy-Dispersive Spectroscopy), Cyclic Voltammetry (CV) and Electrochemical Impedance Spectroscopy (EIS). The introduction of an appropriate intermediate layer, Zr-SnO2, was performed. We also tried to fabricate Ytterbium (Yb) doped Ti/Zr-SnO2/PbO2 electrodes by an electrodeposition method on the intermediate layer of Zr-SnO2. The surface morphology of the Ti/Zr-SnO2/PbO2 electrode was changed due to the Yb doping, which affected the electrocatalytic activity of the modified electrode. Result: The developed Yb-doped Ti/Zr-SnO2/PbO2 electrode showed improved removal efficiencies toward AYR. Conclusion: The effects of current density and initial AYR concentration on the electrochemical oxidation of AYR by Yb-doped Ti/Zr-SnO2/PbO2 were investigated. The removal rate of AYR was 97.3% in 180 min under the conditions of the current density of 60 mA/cm2 , initial AYR concentration of 50.0 mg L-1 , and Na2SO4 concentration of 0.10 mol L-1 .

Contribution of (Bi0.45Y0.05)Na0.5ZrO3 to induced multiphase coexistence and enhanced piezoelectric properties of K0.5Na0.5NbO3 lead-free ceramics

In this study, new lead-free piezoelectric ceramics (1 − x)(K0.5Na0.5)NbO3 (KNN)–x(Bi0.45Y0.05)Na0.5ZrO3 (BYNZ) were prepared using the conventional solid-state method, and the relation between the doping amount of (Bi0.45Y0.05)Na0.5ZrO3 and its structural and electrical properties was investigated. Material characterization and structural analyses conducted using X-ray diffraction, scanning electron microscopy, and energy-dispersive spectroscopy revealed that KNN–BYNZ ceramics formed single perovskite structures at 0 ≤ x ≤ 0.05 and a polycrystalline phase boundary (PPB) for the coexisting orthorhombic and tetragonal phases at 0.03 ≤ x ≤ 0.05. The ceramics exhibited desirable electrical properties at x = 0.04 (d33 = 305 pC/N, kp = 45.8 %, εr = 1316, tanδ = 2.4 %, Tc = 332 °C, Pr = 28.2 μC/cm2, and Ec = 1.07 kV/mm). These findings reveal that the introduction of BYNZ enables the effective formation of a PPB in the KNN-based ceramics to improve their electrical properties, and they exhibit potential for replacing lead-based piezoelectric ceramics in the market.

Optimization of electrical transport and magnetoresistance of La0.72Ca0.28-xPbxMnO3 ceramics by Pb2+ doping

Here, La0.72Ca0.28-xPbxMnO3 (LCPMO, 0 ≤ x ≤ 0.06) polycrystalline ceramics are prepared by the sol-gel method and the influence of Pb2+ doping on microstructure, chemical composition, and electrical transport properties of LCPMO ceramics is systematically investigated. The study was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Energy-Dispersive Spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS) and four-probe method. The four-probe test shows that all samples have MIT (metal-insulator transition) behavior, and the peak resistance gradually decreases with the increase of Pb2+ doping amount. With the increase of Pb2+ doping amount, the temperature coefficient of resistance (TCR) and magnetoresistance (MR) first increased and then decreased, the TCR increased from 24.6 % to 36.5 %·K−1, and the MR value increased from 47 % to 71.5 %, and both corresponded to high temperature direction. Referring to previous studies, higher TCR and MR values near room temperature are what researchers have been pursuing for a long time. it can be seen that the LCPMO ceramics prepared in this article can have good application prospects in infrared detection and magnetic storage.

Experimental study of the vacuum arc motion-diffuse transition in cup-shaped transverse magnetic field contacts

The arc in transverse magnetic field (TMF) contacts transitions to diffusion mode before current zero, affecting arc morphology and motion. TMF-generated force competes with local overheating's stagnation effect, impacting contact surface ablation. Cup-shaped TMF contacts exhibit slow, fast, and unstable transitions. Arc voltage declines gently, rapidly, or in repeated steps. Peak current, contact diameter, contact piece structure, and iron core influence transition characteristics. Transition energy increases linearly with peak current. Larger contact diameter and iron cores make transition constant earlier and transition current higher. Compared to circular contacts, annular contacts delay transition constant and widen transition current range. Scanning electron microscope (SEM) images showed that the ablation cathode surfaces exhibited five morphologies: melting pit, periphery, lamellar, particle, and pore. Energy dispersive spectrum (EDS) analyses show that the periphery has a higher Cu content than the interior, suggesting less Cu loss during fracture and less droplet splashing. The peripheral Cu content is comparable between the two contacts, 62.94 % vs. 62.37 %. However, the interior Cu content of contact NO.4 is higher than NO.6 at 60.54 % vs. 56.26 %. This indicates that the difference in the effect of fast and slow transitions on the cathode surface activity is mainly in the interior region.

Element transfer, microhardness and metallurgical analysis of weld-bead using CaF2−CaO−Al2O3−BaO fluxes

This study investigates the influence of shielded metal arc welding electrode coating flux on microhardness, microstructure and element transfer. A series of multi-pass bead-on-plate studies were conducted using laboratory-developed electrodes. The flux composition has shown a significant effect on all the responses. An increase in [Formula: see text] and [Formula: see text] has shown a positive influence on nickel transfer, whereas an increase in [Formula: see text] reduces nickel transfer. The slag detachability was found good for ratio [Formula: see text]:: 1.76:0.73:0.51. Energy dispersive spectroscopy has shown inclusions rich in aluminum and oxygen with trace amounts of Ca, Mn, Ti and Si. Artificial neural network models have been developed and then compared to conventional regression predictions.

Effect of alloy 625 buffer layer on corrosion resistance of nickel base hardfacing

Nickel base hardfacing alloys serve to mitigate corrosion losses at elevated temperatures. Efficacy of Nickel base hardfacing alloys can be compromised when applied onto Fe base substrates due to iron dilution in hardfacing. The degree of Fe dilution can be reduced by using advanced deposition methods and optimized deposition parameters. Gas Tungsten Arc Welding (GTAW) method is commonly employed for its cost-effectiveness and versatility, but it tends to induce higher Fe dilution due to increased heat input. This study aims to reduce the degree of Fe dilution and enhance corrosion resistance by introducing a nickel base buffer layer (alloy 625) between the nickel base hardfacing alloy and AISI 316L stainless steel substrate. For comparative purposes, Ni base hardfacing alloy was deposited on the substrate without any buffer layer. Hardfacing depositions were prepared using manual GTAW process. Process parameters namely, deposition current, voltage, travelling speed, pre-heating temperature, and cooling method were kept constant. Samples underwent aging at 1123 K for 4 h, followed by microstructural examination via optical and scanning electron microscopes. Iron (Fe) dilution quantification was performed using energy dispersive spectroscopy (EDS). The EDS analysis showed that the use of buffer layer between the hardfaced deposit and the substrate decreased the degree of Fe dilution in the hardfaced deposit. X-Ray diffraction (XRD) analysis was performed to identify various phases formed in the hardfaced deposit. Potentiodynamic polarization test was performed to assess the corrosion resistance of hardfaced deposit in 3.5 wt% NaCl solution. Results show significant improvement in corrosion resistance of hardfacings deposited sample with buffer layer as compared to those without buffer layer. Aging treatment further enhanced corrosion resistance. The corrosion resistance data is correlated with the microstructure and phases formed in various samples.

Characterization and identification of an archaeological “lacquer” pipe

A pipe with red coating on the surface was excavated from an archaeological site in Sweden, which is supposed to be a lacquer ware imported from China due to the admiration and pursue of lacquer wares from Asia by Europeans during sixteenth to eighteenth centuries. However, materials such as shellac and resins were often used to imitate lacquer during that time in Europe. To determine whether the pipe was Chinese lacquer ware or not, attenuated total reflection of fourier transform infrared spectroscopy (ATR-FTIR), thermally-assisted hydrolysis and methylation pyrolysis gas chromatography-mass spectrometry (THM-Py-GC/MS) were conducted. The detection of significant amount of aleuritic acid, laccijalaric acid, laccishellolic acid, shellolic acid and jalaric acid represents that shellac is the main material used for the pipe coating rather than Chinese lacquer. Long chain fatty alcohols were found in the sample, indicating that the shellac is un-dewaxed. In addition, pine resin and turpentine were also found as additives in the pipe coating. Furthermore, pigments in the coating were determined as cinnabar and carbon black by scanning electron microscopy with element energy dispersive spectroscopy (SEM–EDS) and Raman spectroscopy. The results could definitely support the conservation of the pipe, and also provide the evidence of the cultural exchange between Europe and Asia.

A Sustainable Approach for Enhancing Cationic Dyes Adsorption in Single and Multiple Systems using Novel Nano Ferrites Modified with Walnut Shell

AbstractWalnut shell has been used in various experimental studies for different dyes removal, but it is exciting to study the adsorption behaviour of bio‐waste (walnut shell) in combination with spinel zinc ferrite which resulted in the formation of a novel material having magnetic properties and help in easy separation after the wastewater treatment. Novel magnetic walnut shell zinc ferrite (WSZF) composite has been synthesized and used to remove Malachite Green and Methylene Blue from aqueous solution in single and binary dye systems. Different techniques have been used to characterize the composite such as Fourier Transform Infrared Spectroscopy, X‐Ray Diffraction, Field Emission Scanning Electron Microscopy, Energy Dispersive Spectroscopy, Thermogravimetric Analysis and pHzpc. Adsorption of dyes were studied to see the effect of time, pH, adsorbent dose, dye concentration and temperature. The Lagergren pseudo second order model fitted well among various kinetic models employed. Langmuir adsorption isotherm best fitted with maximum adsorption capacities of 86.20 and 169.5 mg/g in single dye and 23.92 and 18 mg/g respectively in binary dye system for Malachite Green and Methylene Blue. Process was spontaneous and ΔH° were found positive, confirmed endothermic process of adsorption. The composite‘s regeneration capacity was studied for five cycles and at the end of five cycle the efficiency of the material was found to be around 80 % for both single as well as binary dye systems. It is concluded that the chosen WSZF will be the optimum solution for cationic dyes removal.

Insights on the effect of process conditions on the optical properties of silver ion exchanged soda-lime silicate glass

The effects of ion exchange time and temperature on the optical properties and plasmonic response of silver ion exchanged soda-lime silicate glass were investigated using scanning electron microscopy (SEM) in energy dispersive spectrometry (EDS) configuration, m-lines spectroscopy, photoluminescence (PL) spectroscopy, and UV–visible absorption spectroscopy. SEM analyses in EDS mode provided profiles of silver oxide molar concentration. These profiles were directly correlated to the silver diffusion coefficient using an adjustment procedure. The effective indices of ion exchanged glasses measured by the standard prism coupling technique (m-lines) allowed access to refractive index distributions in ion exchange regions. These ion-exchanged glasses underwent evaluation to determine their potential suitability for use in multimode planar systems. The PL results acquired after ion exchange demonstrated that the creation of Ag0 atoms from Ag+ ions was responsible for the decline and quenching of PL intensity at ion exchange times and temperatures increase. Silver nanoparticles were generated in the samples subjected to ion exchange at 480 °C without the need for post-exchange treatments. The emergence of the surface plasmon resonance band around 427 nm in the optical absorption spectra confirmed the formation of Ag nanoparticles in annealed glasses. Estimates of the UV–visible absorption spectra indicated an average size of silver nanoparticles ranging from 1.8 to 2.4 nm.

The effect of NaCl concentration on impact-sliding fretting corrosion behavior of Inconel 690TT heat transfer tubes

The effect of NaCl concentration on impact-sliding fretting corrosion behavior of Inconel 690TT heat transfer tubes

Studies on the Authorship of Albumen Vintage Photographs: A Combined Experimental and Chemometric Approach

The differences in albumen photographs from vintage photographic studios were identified by energy-dispersive X-ray fluorescence spectroscopy and Fourier transform infrared spectroscopy. The results inspired the concept of finding common features characteristic of a given photographic studio. The obtained measurement data (i.e., positions of vibrational bands for characteristic groups of albumen and the mass contents of chosen elements) were analyzed chemometrically by employing the Principal Component Analysis (PCA). The PCA technique allowed us to reduce the number of relevant experimental parameters characterizing the unique features of the photographic objects. The two major components were able to distinguish the photographic objects in terms of their authorship and the time to produce a photograph. The method developed was examined for a selected group of photographs consisting of albumen prints from three Polish photographic ateliers. To validate ED-XRF measurements and, consequently, the chemometric findings, reference albumen photo samples were designed and prepared. The empirical functional relationships between the content of photochemically reduced silver particles on the photographic paper and several physicochemical factors, including time of exposure to UV light, AgNO3 concentration in a fixed bath, and concentrations of other additives, were proposed. These results can be used for the prediction of the experimental conditions under which the investigated photographs were developed.

Comparison of microstructure, mechanical, and electrochemical performance of laser-deposited FeCrV15 alloy at varying powder feed rates

In the realm of surface modification, repair, and reinforcement of components exposed to challenging operational conditions, such as tillage tools, laser cladding stands out as an innovative manufacturing technique. Employing this additive manufacturing approach, a functionally graded material with outstanding strength and properties is incorporated to enhance the desired attributes of the base material. This comparative investigation scrutinized and assessed the microstructural characteristics, hardness, wear resistance, and corrosion behavior of high carbon ferrochrome FeCrV15 coatings fabricated at two distinct powder feed rates, namely 5 and 6 g/min, respectively. The analysis delved into how the resultant coatings' molten bead deposition, microstructural evolution, hardness, wear resistance, and corrosion resistance were influenced by the powder feed rate. Evaluation of hardness was conducted using a Vickers microhardness testing apparatus, while phase identification was accomplished utilizing an X-ray diffractometer. The morphologies of the microstructures were scrutinized employing optical microscopy and scanning electron microscopy coupled with energy dispersive spectroscopy (SEM/EDS). Furthermore, the corrosion response of the deposits in a soil–water environment was probed utilizing an Autolab potentiostat. A comprehensive assessment of the coatings' sliding wear performance was undertaken using an Anton Paar Tribometer. The findings of the study reveal that an escalation in the powder feed rate engenders heightened grain refinement within the microstructure, yielding a defect-free sample and augmenting the wear performance (with a wear rate of 2.42 × 10–6 mm3/N/m for sample B, surpassing 2.39 × 10–5 mm3/N/m for sample A and outstripping 1.72 × 10–3 mm3/N/m for the steel substrate). Additionally, the corrosion resistance is enhanced (with a corrosion rate of 0.0032 mm/yr for sample B, surpassing 0.0036 mm/yr for sample A, which, in turn, exceeds 0.1168 mm/yr for the steel substrate) in the case of sample B.

Evaluation of the Combustion Properties and Catalytic Activity of MgAlB Energetic Ternary Particles

ABSTRACT Boron powder possesses significant potential for use as a combustible agent in energetic materials, owing to its superior combustion thermodynamic properties. However, the powder’s tendency to form an oxide layer on its surface results in delayed ignition, reduced combustion efficiency, and compromised energy advantage. To enhance the ignition and combustion properties of boron powder, we prepared boron-based energetic composites containing flammable metals (MgxAl1-xB2) through high-temperature sintering. These were then characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), energy dispersive spectroscopy (EDS). The combustion heat of these alloy powders were measured using an oxygen bomb calorimeter, while their catalytic performance on the thermal decomposition of ammonium perchlorate (AP) was analyzed using differential scanning calorimetry (DSC) and differential thermal analysis (DTA). The results indicate that compared with boron, the MgxAl1-xB2 powders are more flammable, require less oxygen, exhibit a higher combustion efficiency and exothermic advantage. Especially, the Mg0.9Al0.1B2 and MgB2 alloy exhibit optimal combustion heat values of 39,094.92 and 37,693.90 J·g−1, respectively. They significantly enhance the thermal decomposition of AP and reduce the activation energy by over 20%.

Advances in Understanding Tungsten Disulfide Dynamics during the Hydrogen-Evolution Reaction: An Initial Step in Elucidating the Mechanism.

Tungsten disulfide (WS2), a promising electrocatalyst made from readily available materials, demonstrates significant effectiveness in the hydrogen-evolution reaction (HER). The study conducts a thorough investigation using various analytical methods such as scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive spectrometry (EDS), X-ray diffraction (XRD), X-ray absorption spectroscopy (XAS), electron paramagnetic resonance (EPR), and in situ Raman spectroscopy. These techniques have uncovered changes in the WS2 particle structure during HER. Through employing EPR, XAS, and in situ Raman spectroscopy, the research reveals structural and chemical transformations. This includes the formation of novel W species and signs of W-O bond formation. Moreover, significant changes in the morphology of the particles were observed. These findings offer enhanced insights into the mechanisms of WS2 under HER conditions, highlighting its catalytic performance and durability.