Search Results (508)

With the rapid advancement of energy storage technologies, there is a growing demand for affordable, efficient, and environmentally benign battery systems. Sodium-ion batteries (SIBs) present a promising alternative to lithium-ion systems due to sodium’s high abundance and similar electrochemical properties. Particular attention is given to developing NASICON -sodium (Na) super ionic conductor, type cathode materials, especially Na3V2(PO4)3, which exhibits high thermal and structural stability. This study focuses on the sol–gel synthesis of Na₃V₂(PO₄)₃ using citric acid and ethylene glycol, as well as investigating the effect of annealing temperature (400–1000 °C) on its structural and electrochemical properties. Phase composition, morphology, textural characteristics, and electrochemical performance were systematically analyzed. Above 700 °C, a highly crystalline NASICON phase free of secondary impurities was formed, as confirmed by X-ray diffraction (XRD). Microstructural evolution revealed a transition from a loose amorphous structure to a dense granular morphology, accompanied by changes in specific surface area and porosity. The highest surface area (67.40 m²/g) was achieved at 700 °C, while increasing the temperature to 1000 °C caused pore collapse due to sintering. X-ray photoelectron spectroscopy (XPS) confirmed the predominant presence of V³⁺ ions and the formation of V⁴⁺ at the highest temperature. The optimal balance of high crystallinity, uniform elemental distribution, and stable texture was achieved at 900 °C. Electrochemical testing in a Na/NVP half-cell configuration delivered an initial capacity of 70 mAh/g, which decayed to 55 mAh/g by the 100th cycle, attributed to solid-electrolyte interphase (SEI) formation and irreversible Na⁺ trapping. These results demonstrate that the proposed approach yields high-quality Na₃V₂(PO₄)₃ cathode materials with promising potential for sodium-ion battery applications. Full article

Humans have been using lipids for many centuries; these are oils found in plants, particularly in seeds. However, relatively recently, it has become clear that lipids are the primary metabolites of any living organism. Fatty acids (FAs) are a structural component of lipids, and their role in building the framework of the lipid bilayer cannot be overstated. They participate in maintaining homeostasis by controlling membrane permeability. Changes in the FA composition of lipid bilayers can modulate the transition of the membrane from a liquid crystalline to a gel-like state. Thus, knowledge of a plant’s FA profile can aid in understanding the physiological mechanisms underlying their interaction with the environment and the ways in which they adapt to various stress factors. Throughout the colonization of terrestrial habitats, plants evolved, and new phylogenetic groups appeared; at present, some features of the FA composition of their individual representatives are known. However, the overall change in the composition of lipid FAs during the evolution of higher plants is still not understood. Our analysis of the literature showed that the FA diversity tends to decrease from mosses to angiosperms, mainly due to a reduction in polyunsaturated very-long-chain FAs, while the average acyl chain length remains unchanged. It is important to recognize the trends in this process in order to understand the adaptive capabilities of higher plants. This knowledge can be useful not only from a fundamental point of view, but also in practical human activities. Full article

To solve the problem of purifying concentrates of rutile and zircon, a new method of electric separation after thermal activation roasting at 800 °C was proposed to strengthen the separation of Ti/Zr-bearing minerals. The results showed that the grade of TiO₂ in the conductor increased by 2.55~6.45% and the content of ZrO₂ decreased by 0.83~2.60% after thermal activation roasting and electronic separation, in contrast with electronic separation without roasting. To further explore the mechanism of activation roasting, the electrical conductivity, the phase evolution, and the microstructure of the gravity separation concentrate (GSC), pure rutile and pure zircon before and after roasting were investigated. The results of conductivity testing showed that the roasting pretreatment significantly improved the conductive difference between rutile and zircon, thus strengthening their separation performance. The XRD results revealed that the thermal activation roasting made the anatase in the GSC transform into rutile, thus enhancing the conductivity. Meanwhile, the crystallinity of both of the pure minerals was improved. The SEM results showed that the GSC particles formed loose and porous sinters, suggesting the reconstruction of the unstable anatase into rutile. Small amounts of cracks and protrusions occurred on the surface of both pure minerals, ascribed to the dehydration and deoxygenation at a high temperature. Full article

We present a systematic study of the fundamental optical properties of indium selenide (InSe) single crystals over a temperature range of 17 K to 300 K. The high structural quality of the β-polytype crystals was confirmed through X-ray diffraction, Raman spectroscopy, and high-resolution transmission electron microscopy, demonstrating excellent crystallinity and a nearly stoichiometric In:Se ratio. The temperature-dependent absorption and photoluminescence (PL) spectra are characterized by a prominent free exciton (FX) resonance. At 17 K, the photoluminescence spectrum exhibits a distinct fine-structure splitting of the Wannier–Mott exciton, yielding a triplet state at 1.333 eV and a singlet state at 1.336 eV. Additionally, a biexciton (XX) is localized at an energy of 1.322 eV as confirmed by the nonlinear dependence of intensity on excitation power density. At low temperatures, the absorption spectrum exhibits the free exciton ground state (n = 1) at 1.338 eV together with the first excited state (n = 2) at 1.350 eV. We systematically tracked and analyzed the temperature evolution of these quasiparticle energies. These findings enhance our understanding of the intrinsic many-body interactions in high-quality InSe, providing essential parameters for advancing its applications in innovative optoelectronic and quantum light-emitting devices. Full article

Currently, the growing demand for sustainable hydrogen makes the oxygen evolution reaction (OER) increasingly important. To boost the performance of electrochemical cells for water electrolysis, both cathodic and anodic sides need to be optimized. Noble metal catalysts for the OER suffer from high costs and limited availability; therefore, developing efficient, low-cost alternatives is crucial. This work investigates manganese-based materials as potential noble-metal-free catalysts. Mn antimonates, Mn chlorates, and Mn bromates were synthesized using ultrasound-assisted techniques to enhance phase composition and homogeneity. Physicochemical characterizations were performed using X-ray diffraction (XRD) and Scanning Electron Microscopy (SEM), together with energy-dispersive X-ray spectroscopy (EDX) and surface area analyses. All samples exhibited a low surface area and inter-particle porosity within mixed crystalline phases. Among the catalysts, Mn_7.5O₁₀Br₃, synthesized via ultrasound homogenization (30 min at 59 kHz) and calcined at 250 °C, showed the highest OER activity. Drop-casted on Fluorine-Doped Tin Oxide (FTO)-coated Ti mesh, it achieved an overpotential of 153 mV at 10 mA cm⁻², with Tafel slopes of 103 mV dec⁻¹ and 160 mV dec⁻¹ at 1, 2, and 4 mA cm⁻² and 6, 8, 10, and 11 mA cm⁻², respectively. It also demonstrated good short-term stability (1 h) in acidic media, with a strong signal-to-noise ratio. Its short-term stability is comparable to that of the benchmark IrO₂, with a potential drift of 15 mV h⁻¹ and a standard deviation of 3 mV for the best-performing electrode. The presence of multiple phases suggests room for further optimization. Overall, this study provides a practical route for designing noble metal-free Mn-based OER catalysts. Full article

The objective of this study is to systematically investigate the effects of friction stir spot welding (FSSW) parameters—rotational speed, dwell time, and pin diameter—on the mechanical, thermal, and microstructural properties of PA6. PA6 plates (5 mm thick, 30 mm wide, 150 mm long) were welded using an Optimum BF20L milling machine, examining key parameters: rotational speed (762, 1146, 1560 rpm), pin diameter (M10, M12), and dwell time (15 s, 60 s). A full factorial design was employed to analyze their effects. Rotational speed emerged as the most significant factor influencing tensile strength, with an optimal speed of 1146 rpm yielding 72.4 MPa. Dwell time also played a major role, improving flexural strength by 56.5% as it increased from 15 to 60 s (40.6 MPa to 63.6 MPa). Although pin diameter had limited influence on tensile performance, larger pins (M12) promoted higher crystallinity (up to 33.37%) and better thermal distribution. The degree of crystallinity and crystalline lamella thickness (λ) varied, indicating that thermal and structural properties can be tailored through parameter optimization. These findings highlight the potential of FSSW to enhance PA6’s performance characteristics, making it a viable joining method for high-performance applications in the automotive, aerospace, and electronics industries. Further research is encouraged to deepen the understanding of the relationship between welding parameters and microstructural evolution, particularly in relation to crystallization behavior. Full article

The microstructure of polyacrylonitrile (PAN) precursor fibers has a profound influence on the performance of carbon fibers and depends on the spinning processes and processing conditions. This study compared the evolution of the microstructures and performance of PAN fibers between the wet-spinning and dry-jet wet-spinning processes, utilizing scanning electron microscopy, small/wide-angle X-ray scattering, dynamic mechanical analysis, and single-fiber tensile testing. Both spinning processes promoted the oriented alignment of microfibrils and fibrils, improved the crystal arrangement and molecular regularity, and facilitated the transition from a two-phase (crystalline/amorphous) structure to a single-phase structure, thereby gradually improving the fibers’ elastic character and mechanical properties. However, wet-spun fibers exhibited inherent defects (skin-core structure and large voids), which caused surface grooves, radial mechanical heterogeneity, and low breaking elongation during post-spinning. In contrast, dry-jet wet-spun fibers initially had a smooth surface and a homogeneous radial structure, which evolved into well-oriented, radially homogeneous structures during post-spinning. Furthermore, the dry-jet wet-spinning process produced greater increases in crystallinity (46%), crystal size (258%), and orientation index (146%) than the wet-spinning process did. The dry-jet wet-spinning process’s superiority in forming and optimizing the fiber microstructure gives it greater potential for producing high-quality PAN precursor fibers. Full article

Silver thin films are widely utilized in plasmonic, electronic, and catalytic devices due to their excellent conductivity, optical properties, and surface activity. However, the nanostructure and performance of Ag films are highly dependent on deposition parameters, particularly during radio-frequency magnetron sputtering (RF-MS). In this study, we systematically investigate the effects of RF power, sputtering time, and substrate type on the growth behavior, crystallinity, and electrical conductivity of Ag films. Optical emission spectroscopy (OES) and Langmuir probe diagnostics were employed to analyze the plasma environment, revealing the evolution of electron temperature and plasma density with varying RF powers. Structural characterizations using XRD, SEM, and AFM demonstrate that higher RF power results in reduced grain size, increased film density, and improved crystallinity, while deposition time influences film thickness and grain coalescence. Substrate material also plays a key role, with Cu substrates promoting better crystallinity due to improved lattice matching. Electrical measurements show that denser films with larger grains exhibit lower sheet resistance. These findings provide a comprehensive understanding of the plasma–film interplay and offer strategic insights for optimizing silver nanofilms in high-performance optoelectronic and catalytic systems. Full article

Considering the current requirement for high temperatures and the significant energy consumption in the preparation of geopolymer-based cements, this paper presents a study on the compressive strength of metakaolin-based geopolymers containing various low-calcium fly ash admixtures, prepared at room temperature (25 ± 2 °C). The physical properties and microstructure of the geopolymers were characterized using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and energy dispersive X-ray spectroscopy (EDS). The type of alkaline cations, phase transformation, evolution of characteristic functional groups, and hydration characteristics of the microstructures were analyzed, and the hydration mechanism is discussed. The experimental results indicated that the fly ash content had a more significant impact on compressive strength than the alkaline cation type (Na⁺/K⁺). The optimal formulation (20% fly ash with 20% KOH activator) reached a compressive strength of 76.70 MPa at 28 days, which was around 6% higher than that of the NaOH-activated counterpart (72.34 MPa). Crystalline phase analysis in the transformation of mullite and microstructure analysis indicated that the increase in compressive strength could be attributed to the effective filling of the matrix interface by chemically inert fillers and the dense N-A-S-H and C-(A)-S-H multi-dimensional gel structures. These experiments prove the feasibility of using fly ash and metakaolin to prepare geopolymer materials with high compressive strength at room temperature. Full article

This study explores the synthesis of copper oxide nanoparticles (CuO NPs) via green and conventional methods, with emphasis on their performance in hydrogen evolution reactions (HERs). CuO NPs synthesized using okra extract (CuO_okra) and hydrazine hydrate (CuO_hyd) were characterized using XRD, FTIR, SEM, HRTEM, and electrochemical techniques. Structural analysis revealed that CuO_okra NPs have smaller crystallite sizes (39.8 nm) and higher defect densities than CuO_hyd NPs (56.8 nm), while CuO_hyd exhibited superior porosity and crystallinity. In HER studies, CuO_hyd outperformed CuO_okra, achieving a significantly lower overpotential (342.2 mV vs. 408.49 mV at 20 mA cm⁻²) and higher cathodic current density (15.9 vs. 11.3 mA cm⁻² at −1.3 V). Electrochemical impedance spectroscopy (EIS) further confirmed the superior catalytic activity of CuO_hyd NPs, showing minimal polarization resistance compared to CuO_okra. Full article

Geopolymers represent an innovative and environmentally sustainable alternative to traditional construction materials, offering significant potential for reducing anthropogenic CO₂ emissions. Among these, phosphoric acid-activated metakaolin-based systems have attracted increasing attention for their chemical and thermal resilience. In this study, we present a comprehensive structural and mechanical evaluation of metakaolin-based geopolymers synthesized across a wide range of Al/P molar ratios (0.8–4.0). Six formulations were systematically prepared and analyzed using X-ray powder diffraction (XRPD), small-angle X-ray scattering (SAXS), Fourier-transform infrared spectroscopy (FTIR), solid-state nuclear magnetic resonance (ssNMR), and complementary mechanical testing. The novelty of this work lies in the integrated mapping of composition–structure–property relationships across the broad Al/P spectrum under controlled synthesis, combined with the rare application of SAXS to reveal composition-dependent nanoscale domains (~18–50 nm). We identify a stoichiometric window at Al/P ≈ 1.5, where complete acid consumption leads to a structurally homogeneous AlVI–O–P network, yielding the highest compressive strength. In contrast, acid-rich systems exhibit divergent flexural and compressive behaviors, with enhanced flexural strength linked to hydrated silica domains arising from metakaolin dealumination, quantitatively tracked by ²⁹Si MAS NMR. XRPD further reveals the formation of uncommon Si–P crystalline phases (SiP₂O₇, Si₅P₆O₂₅) under low-temperature curing in acid-rich compositions. Together, these findings provide new insights into the nanoscale structuring, phase evolution, and stoichiometric control of silica–alumino–phosphate geopolymers, highlighting strategies for optimizing their performance in demanding thermal and chemical environments. Full article

Protective coatings are essential for extending the service life of components exposed to harsh conditions, such as pipes used in industrial systems, where wear and corrosion remain constant challenges. This study explores the development of a nano-sized TiO₂-reinforced electroless nickel-based ternary (Ni-W-P) alloy and composite coating on API X60 steel, a high-strength carbon steel pipe grade widely used in oil and gas pipelines, using an alkaline hypophosphite-reduced bath. The surface morphology, microstructure, elemental composition, structure, phase evolution, adhesion, and roughness of the coatings were analyzed using optical microscopy, FESEM, EDS, XRD, AFM, cross-cut tape test, and 3D profilometry. The tribological performance was evaluated via Vickers microhardness measurements and reciprocating wear tests conducted under dry conditions at a 5 N load. The TiO₂ nanoparticle-reinforced composite coating achieved a consistent thickness of approximately 24 µm and exhibited enhanced microhardness and reduced coefficient of friction (COF), although the addition of nanoparticles increased surface roughness (S_a). Annealing the electroless composites at 400 °C led to a significant improvement in their tribological properties, primarily owing to the grain growth, phase transformation, and Ni₃P crystallization. XRD analysis revealed phase evolution from an amorphous state to crystalline Ni₃P upon annealing. Both the alloy and composite coatings exhibited excellent adhesion performances. The combined effect of TiO₂ nanoparticles, tungsten, and Ni₃P crystallization greatly improved the wear resistance, with abrasive and adhesive wear identified as the dominant mechanisms, making these coatings well suited for high-wear applications. Full article

The CaO-SiO₂-P₂O₅ system is one of the main systems studied aiming for the synthesis of new bioactive materials for bone regeneration. The interest in materials containing calcium-phosphate-silicate phases is determined by their biocompatibility, biodegradability, bioactivity, and osseointegration. The object of the present study is the synthesis by the sol-gel method of biocompatible glass-ceramics in the Ca₂SiO₄-Ca₃(PO₄)₂ subsystem with the composition 6Ca₂SiO₄·Ca₃(PO₄)₂ = Ca₁₅(PO₄)₂(SiO₄)₆. The phase-structural evolution of the samples was monitored using X-ray diffraction analysis (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS), and surface area analysis. A powder (20–30 µm) glass-ceramic material containing fine crystalline aggregates of dicalcium silicate and plates of silicon-substituted hydroxyapatite was obtained after heat treatment at 700 °C. After heat treatment at 1200 °C, Ca₁₅(PO₄)₂(SiO₄)₆, silicocarnotite Ca₅(PO₄)₂(SiO₄), and pseudowollastonite CaSiO₃ were identified by XRD, and the particle size varied between 20 and 70 µm. The compact glass-ceramic obtained at 1400 °C contained Ca₂SiO₄-Ca₃(PO₄)₂ solid solutions with an α-Ca₂SiO₄ structure as a main crystalline phase. SEM showed the specific morphology of the crystalline phases and illustrated the trend of increasing particle size depending on the synthesis temperature. Effects of the glass-ceramic materials on cell viability of HL-60-derived osteoclast-like cells and on the expression of apoptotic and osteoclast-driven marker suggested that all materials at low concentrations, above 1 µg mL⁻¹, are biocompatible, and S-1400 might have a potential application as a scaffold material for bone regeneration. Full article

Iron, an essential element for virtually all known organisms, serves not only as a micronutrient but also as an energy source for bacteria. Iron-oxidizing microorganisms mediate Fe(II) oxidation under diverse redox conditions, yielding amorphous iron (hydr)oxides or crystalline iron minerals. This globally significant biogeochemical process drives modern iron cycling across terrestrial and aquatic ecosystems. The resulting biomineralization not only produces secondary minerals but also effectively immobilizes heavy metals, offering a sustainable strategy for environmental remediation. This review systematically examines (1) the biogeochemical mechanisms and mineralogical signatures of Fe(II) oxidation by four distinct iron oxidizers: acidophilic aerobes (e.g., Acidithiobacillus), neutrophilic microaerophiles (e.g., Gallionella), nitrate-reducing anaerobes (e.g., Acidovorax), and anoxygenic phototrophs (e.g., Rhodobacter); (2) research advances in heavy metal immobilization by biogenic iron minerals: adsorption, coprecipitation, and structural incorporation; and (3) the impact of pH, temperature, organic matter, and coexisting ions on Fe(II) oxidation efficiency and iron mineral formation by iron-oxidizing bacteria. By characterizing iron-oxidizing bacterial species and their functional processes under varying pH and redox conditions, this study provides critical insights into microbial behaviors driving the evolution of acid mine drainage (AMD). Full article

Electrocatalytic water splitting has been demonstrated to be a highly efficient and promising technology for green hydrogen production. However, the inefficiency and instability of the cathode hinder its wide application in water electrolysis. Herein, we report a rapid Joule heating method for synthesizing the Ru-Mo oxide catalyst. Comprehensive characterization results confirmed that the as-prepared catalyst featured an internal porous structure with low crystallinity, which weakened the strength of Ru-H bonds through structural and electronic modulation. The enhanced HER performance was attributed to the incorporation of Mo⁴⁺ species, which strengthened Ru-O-Mo interactions. As tested, the optimized catalyst exhibited ultralow overpotentials (25.08 mV and 120.52 mV @ 10 and 100 mA cm⁻², respectively) and excellent stability (100 h @ 100 mA cm⁻²) in a 1 M KOH solution. Meanwhile, the as-prepared catalyst was equipped in an anion exchange membrane (AEM) alkaline water electrolyzer, which could deliver 185 mA cm⁻² at only 2.16 V with 100% Faradaic efficiency. This study provides a feasible strategy for constructing highly efficient low-crystallinity electrocatalysts. Full article