Search Results (584)

Monometallic nanoparticles tend to aggregate and exhibit limited catalytic performance, rendering them inadequate for high-efficiency electrocatalytic applications. In this study, a green and mild liquid-phase reduction method was employed, using sodium borohydride to simultaneously reduce graphene oxide (GO) and metal precursors. This approach enabled the uniform and highly dispersed loading of silver–copper bimetallic alloy nanoparticles (Ag_1−xCu_x NPs) onto the surface of reduced graphene oxide (RGO). By tuning the Ag/Cu molar ratio, the size, composition, and morphology of the nanoparticles were precisely controlled. Characterization by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) confirmed that GO was efficiently reduced to RGO, and the bimetallic nanoparticles were uniformly distributed on the RGO surface in an alloy state with small particle size and no obvious agglomeration. A strong interfacial interaction between the metal nanoparticles and the support was also observed. Electrochemical tests demonstrated that the composite exhibits excellent electrocatalytic activity toward the reduction of H₂O₂. Notably, the reduction peak current at the Ag_0.5Cu_0.5NPs/RGO modified electrode was 1.8 and 2.3 times higher than those at the monometallic Ag/RGO and Cu/RGO electrodes, respectively. These results provide a reliable theoretical basis and a viable research route for the controllable synthesis of low-cost, high-performance electrocatalytic nanocomposites and their application in electrochemical H₂O₂ sensing. Full article

The escalating global demand for renewable energy has positioned solar photovoltaics (PV) as a critical technology for achieving net-zero emissions. However, PV efficiency is strictly limited by thermal degradation, where elevated operating temperatures significantly reduce power output and accelerate material aging. This review systematically evaluates the integration of advanced phase change materials (PCMs) as a passive thermal management solution. We analyze the transition from material-level innovations—including nano-enhanced PCMs, 3D conductive frameworks, and shape-stabilization—to system-level hybrid architectures such as liquid—PCM, heat pipe-fin, and thermoelectric generator (TEG) integrations. Synthesis of recent empirical data (2024–2026) demonstrates that optimized PCM composites can achieve PV temperature reductions of up to 32 °C and electrical efficiency enhancements exceeding 19%. Furthermore, techno-economic assessments reveal that these systems can reduce the levelized cost of energy (LCOE) by 5–15% and achieve energy payback times as short as 1.5 years. Finally, this paper identifies critical research gaps in long-term outdoor durability, AI-driven predictive modeling, and sustainable bio-based encapsulation, providing a strategic roadmap for the commercialization of next-generation solar thermal management systems. Full article

TIDEs (therapeutic peptides, oligonucleotides, and related molecules) represent a rapidly expanding market that has gained significant momentum due to the recent success of Glucagon-like peptide-1 (GLP-1) receptor agonists for the treatment of obesity, diabetes and as cardiovascular and kidney diseases. Chemical synthesis remains the dominant manufacturing route for candidates containing approximately 10–40 amino acids and includes non-proteinogenic amino acids. Consequently, various combinations of solid-phase peptide synthesis (SPPS), liquid-phase peptide synthesis (LPPS), hybrid approaches, or tag-assisted peptide synthesis (TAPS) can be applied to achieve full-sequence assembly. However, identifying the most eco-efficient pathway through experimental trials alone is impractical because of the vast number of possible process combinations and the growing variety of green solvent alternatives. Therefore, process simulation studies—widely established in chemical engineering—must be adapted to the specific physicochemical characteristics of these large, multi-component molecules. This paper provides an overview of the current state of research and illustrates potential process improvements enabled by digital twin technologies as exemplified for the first manufacturing steps of tirzepatide. Full article

Polymeric fibers represent a vital class of functional materials due to their versatile properties, such as wide availability, low cost, recyclability, biodegradability, and excellent mechanical and chemical stability. Polymer fibers can be fabricated at both micro- and nanoscale dimensions using a variety of processing techniques. This review provides a comprehensive overview of the principal methods employed for polymer fiber preparation, including electrospinning, melt and solution blowing, dry and wet spinning, template synthesis, phase separation, and self-assembly. The technical principles, as well as the advantages and limitations, of each technique are systematically discussed. The review also explores polymeric fibers as smart materials for actuation applications. Particular focus is given to stimulus-responsive fiber systems such as shape memory fibers, hydrogel fibers, liquid crystal fibers, and electroactive polymers. Overall, this review establishes a coherent framework linking polymer fiber fabrication strategies with structure–property–function relationships, offering practical guidance for material selection and accelerating the development of next-generation smart polymer fibers for advanced actuation and multifunctional applications. Full article

The present study extends the investigation of thermodynamic properties of phases in the silver–magnesium binary system, with particular emphasis on the κ-Ag₂Mg₅ phase, for which available literature data remain scarce. The work is divided into two parts. The experimental section comprises the synthesis of the κ phase from high-purity Ag and Mg, followed by its characterisation using scanning electron microscopy (SEM) and X-ray diffraction (XRD). The synthesised material was subsequently used for calorimetric determination of the standard enthalpy of formation employing the drop solution method. Measurements were carried out in two experimental series (A and B), using two different metallic solvents (Al and Sn), at temperatures of 1020 K and 689 K. The enthalpy of formation obtained in both series was −14.4 ± 0.32 and −14.5 ± 0.42 kJ/mol at., respectively. In addition, the limiting partial enthalpy of solution of liquid Ag in liquid Al was determined calorimetrically and its average value is equal 7.1 ± 0.7 kJ/mol. The theoretical part of the study involved ab initio calculations of defect formation energies. The obtained results show good agreement with available literature data and provide a consistent interpretation of the observed non-stoichiometry of the κ-phase. Full article

Plasma-assisted nitrogen fixation has emerged as a promising strategy for sustainable nitrate production. However, the coexistence of multiple interfaces and complex multi-step reaction pathways within the plasma-liquid system often leads to the formation of mixed nitrogen species, posing a significant challenge for achieving high product selectivity. In this study, a dual-cell reactor was introduced in liquid-phase plasma (LPP) system, enabling selective product distribution. Optical emission spectroscopy revealed pronounced signals corresponding to the second positive system (SPS) of N₂ and the first negative system (FNS) of N₂⁺, indicative of strong plasma excitation and ionization processes that facilitated the formation of reactive nitrogen oxide intermediates. These species were subsequently converted into aqueous NO₂⁻ and further oxidized into NO₃⁻ only in the reaction cell where reactive species are generated. The effects of key parameters, including electrode material, treatment time, solution pH, and discharge conditions, were comprehensively evaluated. As a result, the reaction cell achieved a nitrate selectivity of 98.9%, whereas the absorption cell achieved a nitrite selectivity of 100%. Findings from EPR and scavenger analyses collectively provide a detailed mechanistic understanding of LPP-driven nitrogen fixation and highlight the importance of controlling plasma parameters to achieve highly selective production of nitrogen compounds. Full article

Since the first successful synthesis of borophene in 2015, this atomically thin boron allotrope has attracted extensive attention due to its polymorphic structures, metallic conductivity, and outstanding mechanical flexibility. As a new member of the two-dimensional (2D) materials family, borophene exhibits a unique triangular lattice with tunable hexagonal vacancies, leading to rich structural diversity and anisotropic physical properties. Recent breakthroughs in synthesis—particularly molecular beam epitaxy (MBE), chemical vapor deposition (CVD), and solvothermal-assisted liquid-phase exfoliation (S-LPE)—have significantly expanded the accessible structural phases and improved control over film quality and stability. Meanwhile, borophene’s distinctive combination of structural and electronic characteristics has enabled its rapid development in both energy and biomedical applications. In energy storage, borophene serves as a promising anode material for lithium/sodium-ion batteries and a lightweight medium for hydrogen storage and supercapacitors, owing to its metallic conductivity, high surface charge density, and large adsorption capacity. In biomedicine, borophene-based nanoplatforms exhibit excellent photothermal conversion efficiency, enabling multifunctional roles in cancer diagnosis and therapy. Despite these advances, several challenges—such as environmental instability, oxidation susceptibility, and limited scalable synthesis—continue to restrict practical implementation. Future progress will depend on chemical functionalization, surface passivation, and machine-learning-assisted materials design to achieve oxidation-resistant, large-area, and biocompatible borophene derivatives. This review summarizes recent advances in borophene synthesis, structural engineering, and multifunctional applications, while outlining key scientific challenges and future opportunities for the realization of borophene-based materials in next-generation energy and biomedical systems. Full article

The scalable production of high-quality nanoparticles is a significant challenge for advancing nanotechnology applications. This research introduces a continuous-flow liquid-plasma discharge reactor for the synthesis of silver nanoparticles at room temperature and atmospheric pressure, utilizing D-xylose as a dual-function reducing and stabilizing agent. The reactor effectively generated uniform xylose-capped silver nanoparticles (X-Ag NPs). Optimal conditions were established utilizing argon gas at a 1:100 molar ratio of Ag precursor to D-xylose, resulting in spherical X-Ag NPs with an average size of 16.89 nm, a zeta potential of −38.87 mV, and a polydispersity index of 0.22. The formation and properties of X-Ag NPs were confirmed through characterization techniques including UV-Vis spectroscopy, dynamic light scattering (DLS), Fourier-transform infrared spectroscopy (FT-IR), and scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDS). The findings demonstrate that uniform particle nucleation and growth occurred due to the homogeneous distribution of high-energy electrons and reactive gas species produced in the plasma phase. This environmentally sustainable, continuous-flow method shows considerable promise for the industrial-scale production of biomass-derived silver nanoparticles. Full article

The discovery of melatonin as a multifunctional free radical scavenger and its possible synthesis in the mitochondrial matrix of peripheral eukaryotic somatic cells highlights a critical new perspective on the importance of this indole. Experimental evidence supporting these findings is substantial, but there are still lingering questions whether melatonin is a direct radical scavenger in vivo and whether it is synthesized in the mitochondrial matrix. We systematically analyze the innovative experimental approaches that support melatonin’s radical scavenging actions and assess the compelling data supporting its production in mitochondria. Melatonin concentrations are reportedly higher in this organelle than in other cellular compartments. Proteins for the enzymes required to convert serotonin to melatonin are present in the mitochondrial matrix and purified mitochondria synthesize melatonin. In the mitochondrial matrix, melatonin is likely located within the “damage radius” of highly reactive oxygen species. We also summarize novel actions of melatonin associated with its regulation of membrane fluidity, determine the molecular composition of membrane lipid rafts, and modulate liquid–liquid phase separation and biomolecular condensates intracellularly. If the findings discussed herein continue to be validated, melatonin would be in an optimal position to function as an antioxidant and may be a key driver in the context of preserving mitochondrial redox homeostasis and disease mitigation. Full article

This study addresses the synthesis of a new liquid crystalline compound featuring a 3,5-disubstituted isoxazoline and a 1,3-dioxolan-2-one ring, and renewable aromatic building blocks derived from vanilin and benzoic acid. The target compound was synthesized through a multistep synthetic route involving alkylation, esterification, oxime formation, and a 1,3-dipolar cycloaddition reaction. The synthesized compound, 2-methoxy-4-[5-(2-oxo-1,3-dioxolan-4-yl)-4,5-dihydroisoxazol-3-yl]phenyl 4-n-decyloxybenzoate, was isolated and fully characterized by spectroscopic techniques. Liquid crystal behavior was evaluated by DSC and POM. The monotropic mesomorphic behavior of the title compound was dictated by the interplay between molecular architecture and intermolecular organization, with the methoxy substituent and the 1,3-dioxolan-2-one ring critically influencing phase stability and texture morphology. These findings suggest a structure–property relationship and guide ongoing synthetic optimization toward achieving a stable enantiotropic liquid-crystalline phase and further ion-conduction experiments. Full article

Ultrafine spherical Ag powders with narrow particle size distribution, high tap density, and limited agglomeration are important conductive fillers for advanced photovoltaic paste formulation. Current liquid-phase reduction scale-up is limited by uncontrolled nucleation, secondary agglomeration, and precursor passivation. This study investigates a process-integrated synthesis chain from precursor preparation to pilot-scale powder production from precursor preparation to kilogram-scale production. A flow-field-enhanced dissolution process (70–80 °C, 30–40% HNO₃) alleviates silver ingot passivation, while a multi-stage NaOH spray system reduces NO_x emissions to 186 mg/m³, meeting GB31573-2015 standards. Ascorbic acid kinetically decouples nucleation and growth per the LaMer model. Molecular dynamics simulations and RDF analysis reveal a synergistic dispersion mechanism involving PVP and gum arabic. A purpose-built 20 L pilot reactor with optimized fluid dynamics and high-pressure cleaning eliminates supersaturation heterogeneity. Subsequent ethanol displacement and supersonic jet milling yield 1 kg-scale powder with D50 = 1.90 µm, tap density = 6.0 g/mL, specific surface area = 0.6 m²/g, and LOI (538 °C) = 0.98%. The obtained powder shows powder-level characteristics relevant to subsequent photovoltaic paste formulation, rather than direct device-level validation. Full article

Background: Prostate cancer remains a significant global health burden, yet current diagnostic reliance on PSA screening is heavily hampered by limited specificity and high rates of overdiagnosis. Methods: To address this clinical bottleneck, we utilized a highly sensitive Complete360^®-MyMeta targeted-metabolomics platform to perform high-resolution profiling of 43 metabolites across the carnitine, polyamine, and methylation networks in plasma from a discovery cohort of all-stage (I–IV) PCa patients and healthy controls. Results: Our analysis identified 28 significantly altered metabolites (p < 0.05), revealing profound systemic metabolic reprogramming characterized by the depletion of circulating TML and putrescine, alongside the elevation of L-acetylcarnitine and sarcosine. These systemic shifts are consistent with a localized tumoral “metabolic sink”, wherein upregulated mitochondrial TML import via the SLC25A45 transporter actively fuels fatty acid oxidation, while parallel androgen signaling drives massive polyamine synthesis. Translating these mechanistic insights into a clinical tool, we developed a multivariable diagnostic signature utilizing mathematically stable bipartite metabolic ratios. An optimized, cross-validated model combining L-acetylcarnitine/TML and sarcosine/putrescine effectively mitigated physiological noise to achieve robust diagnostic separation, yielding an area under the curve (AUC) of 0.99. Conclusions: Ultimately, this study provides a discovery-phase proof-of-concept for the SLC25A45-TML axis as a mechanistically grounded, stage-independent liquid biopsy, offering a rational, non-invasive framework to significantly improve PCa detection. Full article

This work presents a novel one-step plasma–solution synthesis of Prussian Blue (PB) and copper hexacyanoferrate (Cu-PBA) nanoparticles via underwater pulsed DC discharge. For the first time, the direct plasma-assisted formation of these coordination polymers is reported. The obtained materials were examined by X-ray diffraction, Fourier-transform infrared spectroscopy, Raman spectroscopy, and scanning electron microscopy (SEM). These analyses confirmed that the desired phases had formed, along with small amounts of oxide byproducts (α-Fe₂O₃, CuO) arising from the erosion of the electrodes. Photocatalytic activity was evaluated through the degradation of organic dyes (Reactive Red 6C, Rhodamine B, and Methylene Blue) under UV-light irradiation. Both catalysts achieved complete dye degradation within 90 min of UV irradiation (after an initial 30 min dark adsorption step, total experiment time 120 min). Notably, selective performance was observed: PB exhibited higher activity toward the cationic dye Methylene Blue, while Cu-PBA was more effective for the anionic dye Reactive Red 6C. This selectivity is attributed to the specific oxide impurities forming heterojunctions that facilitate charge separation and generate distinct reactive oxygen species. The plasma–liquid method offers a rapid and environmentally benign route to functional PBA-based composites, with potentially scalable characteristics pending further engineering optimization. These findings highlight the potential of utilizing synthesis-induced impurities to tailor photocatalytic selectivity for water purification applications. Full article

Meltable metal–organic frameworks (MOF) are essential for the formation of MOF glasses, which have emerged as a new family of functional materials offering promising potential for applications in gas separation, luminescence, energy storage, and beyond. Herein, the synthesis of iron-based zeolitic imidazolate framework (ZIF) crystals, specifically Fe₃(Im)₆(HIm)₂, where Im is imidazolate, is reported. Upon the substitution of some Im linkers with a secondary ligand, 5,6-dimethylbenzimidazole (dmbIm), it was found that such substitution induces the formation of new phases: one phase exhibits meltability and subsequent glass formation, while another phase [Fe₃(Im)_1.56(dmbIm)_4.44(HIm)₂] is non-meltable. Through structural characterizations, the configuration of the tetrahedral [Fe-linkers] units was revealed to be crucial in determining the meltability of Fe-ZIF. The incorporation of a large secondary ligand hinders the occurrence of melting. This work provides an insight into how ligands affect the accessibility of the liquid state of MOFs, showing a practical strategy for designing meltable MOFs. Full article

This research systematically investigated the catalytic pyrolysis of Arab Heavy (AH) and Arab Light (AL) crude oils using NiO supported on Al₂O₃ or ZSM-5 in a microwave-assisted reactor, with particular emphasis on hydrogen (H₂) generation and value-added chemicals. To understand how both the catalyst and feedstock affect reaction products, gas and liquid products as well as catalyst activity were carefully examined. The production of H₂ and olefins was significantly enhanced by the NiO/Al₂O₃ catalyst, especially when using AL crude. This is most likely due to favorable metal-support interactions that increase the dehydrogenation activity. However, when paired with lighter feedstock, NiO/ZSM-5 greatly increased paraffin production and encouraged light alkane synthesis in both phases. GC-MS and FTIR spectroscopy confirmed that NiO/Al₂O₃ produced liquid products richer in aromatics while also containing a significant fraction of paraffins. Remarkably, the AL over NiO/Al₂O₃ combination showed very little liquid recovery, indicating that gas generation was higher in these reaction conditions. These results showed how H₂ selectivity and hydrocarbon routes in NiO/ZSM-5 and NiO/Al₂O₃ are controlled by various microwave-catalyst interactions. This work further highlights the importance of matching catalyst properties with feedstock type to control product selectivity, with NiO/Al₂O₃ showing particular promise for H₂-focused applications. Full article