Search Results (888)

Europium (Eu) is a rare-earth element with unique optoelectronic properties that underpin its applications in displays and lighting, X-ray imaging, anti-counterfeiting, and biomedicine. Conventional methods typically involve the synthesis of europium-based luminescent materials in powder or crystalline form via high-temperature solid-state reactions or solution processes, followed by secondary processing such as spin coating or evaporation to fabricate films or devices. In this work, we report a direct approach to prepare trivalent europium-based luminescent materials using divalent europium bromide (EuBr₂) as the precursor via a gas-phase vacuum evaporation approach (GPVEA). This “deposition-as-synthesis” method enables the fabrication of the hybrid nanoscale films with various blending ratios, which exhibit changes in the fine structure of the emission peaks. The luminescence spectra remain nearly identical across the temperature range from 80 K to 320 K. The photoluminescence emission intensity is stronger in air than in a vacuum. The films show a maximum photoluminescence quantum yield (PLQY) of 8.27% and good photostability, with an emission decay of 3.44% over 50 min under continuous 300 nm excitation. Through patterned design, we demonstrate their value for anti-counterfeiting applications. This work thus provides guidance for the preparation of europium-based luminescent nanomaterials via GPVEA and their application in anti-counterfeiting. 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

In this work, ZnO nanoparticles were synthesized via a plant-mediated green route using Prosopis tamaulipana extract as a reducing and stabilizing agent and subsequently modified with silver to obtain Ag-modified ZnO powders. Structural and morphological characterization techniques confirmed the formation of nanocrystalline ZnO with a hexagonal wurtzite structure, submicrometric agglomerates composed of nanosized primary particles and a high degree of phase purity, indicating the effectiveness of the synthesis approach. The photocatalytic performance of the Ag-modified ZnO materials was evaluated under natural solar irradiation using methylene blue as a model organic contaminant in aqueous solution. Visual observations, together with absorbance, temperature and electrical conductivity measurements, demonstrated an effective and progressive degradation of the dye over a 5 h irradiation period. The observed increase in electrical conductivity under illumination was associated with enhanced charge carrier generation and improved separation efficiency, as well as the formation of reactive oxygen species, promoted by the presence of Ag as an electron sink. These results confirm that green-synthesized Ag-modified ZnO nanoparticles exhibit enhanced photocatalytic activity and are promising multifunctional materials for sustainable water sanitation applications. Full article

The growing demand for efficient and sustainable energy storage systems has intensified research on advanced materials for lithium–ion batteries (LIBs). Gel-based synthesis routes—particularly polymeric and chelating gel techniques—have emerged as powerful methods for designing lithium–ion battery (LIB) anode materials with tailored microstructures, composition uniformity, and enhanced electrochemical performance. These methods facilitate the transformation of solution-phase precursors into homogeneous and finely structured materials, enabling precise tuning of physicochemical properties. This review provides a comprehensive overview of the fundamental principles of polymeric and chelate gel synthesis routes, highlighting their ability in controlling particle size, morphology, and phase purity. Their applicability to a wide range of anode materials, including transition metal oxides and silicon-based composites, is discussed. The manuscript highlights LIBs anode material developments via gel precursor chemistry, structure–property relationships, and future directions toward scalable and sustainable electrode manufacturing. 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 subject of this study is the electrochemical synthesis of samarium–cobalt (Sm-Co) alloy coatings on a copper substrate from aqueous solutions using chronoamperometric methods. The study focused on assessing the effect of ecological complexing agents—L-arginine and glycine—on the deposition kinetics and quality of the deposits obtained within a potential range of −1.1 V to −1.8 V vs. Ag/AgCl. Morphological analyses indicated that the type of amino acid used determines the layer growth mechanism. It was found that exceeding the potential of −1.4 V results in a rapid increase in samarium content in the alloy, reaching maximum values of 29 at.% for the system with L-arginine and 35 at.% for the system with glycine at a potential of −1.8 V. X-ray Diffraction (XRD) structural studies confirmed the successful synthesis of the Co_8.5Sm intermetallic phase directly by electrodeposition, while X-ray Photoelectron Spectroscopy (XPS) analyses indicated the presence of oxides and hydroxides on the deposit surface. Despite obtaining a high samarium content, it was observed that intense hydrogen co-evolution at low potential leads to a decrease in current efficiency and the formation of internal stresses and cracks in the structure of the coatings. Full article

Heavy metal contamination of water by cadmium (Cd²⁺) and silver (Ag⁺) represents a significant environmental concern due to their toxicity and persistence. In this study, peptide-functionalized resins were evaluated as bio-inspired adsorbent materials for metal removal from aqueous solutions. Glycine-based and histidine-containing peptide sequences were synthesized via solid-phase peptide synthesis and immobilized onto Wang and Rink amide resins, with and without N-terminal acetylation. Adsorption capacity (Q, mg g⁻¹) was determined for each material. The results showed that adsorption performance strongly depends on both peptide structure and metal type. Higher adsorption capacities were consistently observed for Cd²⁺ (up to 7.9 mg g⁻¹) compared to Ag⁺ (up to 2.4 mg g⁻¹). Interestingly, histidine-containing resins exhibited superior performance, likely due to the presence of imidazole groups that enhance metal coordination. In contrast, the influence of resin type and N-terminal acetylation was less consistent, suggesting a secondary role of these factors. Overall, the findings provide an initial screening or proof-of-concept for peptide-functionalized resins and highlight the potential of these peptidyl resins as effective adsorbent materials for the removal of heavy metals from aqueous environments. Full article

Achieving a circular and climate-neutral bioeconomy by 2050 requires not only high-quality recycling but also the large-scale integration of renewable carbon from biomass and atmospheric CO₂ into material systems. Plastics represent the world’s largest and most rapidly growing carbon sink, positioning them as a critical intervention point for replacing fossil-based feedstocks with renewable alternatives. Because plastic packaging is one of the most visible material streams encountered by consumers in daily life, a transition toward sustainable, recyclable bioplastics has the potential to deliver both meaningful environmental benefits and strong societal impact, accelerating public awareness and acceptance of renewable carbon solutions. Poly(ethylene furanoate) (PEF)—a fully bio-based polyester synthesized from plant-derived 2,5-furandicarboxylic acid (FDCA) and monoethylene glycol (MEG)—offers a promising pathway toward more sustainable packaging due to its superior mechanical strength and gas-barrier performance relative to polyethylene terephthalate (PET). This study presents a cradle to grave life cycle assessment (LCA) of PEF resin production and PEF bottle applications, using industrially relevant, at-scale process data covering biomass feedstock conversion, polymer synthesis, packaging manufacture, use phase, and end of life. Bottle applications were selected as a focal point due to their technical maturity, commercial relevance, and suitability for direct comparison with incumbent PET systems. The results indicate that PEF can reduce greenhouse gas emissions by up to 71% and fossil resource depletion by 26% compared to PET at the resin level when biogenic carbon uptake is included. Moreover, the material’s enhanced functional properties enable lightweight, recyclable bottle designs with carbon footprint reductions of up to 88% for 500 mL formats under a baseline recycling rate scenario of 72%, with the remaining share directed to municipal solid-waste incineration with energy recovery. Sensitivity analyses reveal that virgin PEF maintains environmental advantages over PET even when PET incorporates high levels of recycled content, highlighting the complementary roles of renewable carbon and circular material strategies. Prospective scenario modeling underscores the importance of sustainable feedstock selection and process electrification, with sucrose-based routes offering the largest potential for further decarbonization. Overall, the findings demonstrate that PEF is a scalable biopolymer capable of delivering substantial climate benefits while supporting circularity objectives. By targeting a highly visible consumer application—plastic packaging—this transition amplifies the societal impact of adopting renewable carbon materials. The study provides actionable insights for policymakers, industry stakeholders, and sustainability practitioners working to advance a more resilient, renewable, and consumer-recognizable plastics economy. 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

Real-time binaural beat synthesis in dynamic acoustic environments is challenged by carrier non-stationarity, interaural phase discontinuities, and processing delay in conventional digital signal processing pipelines. This study proposes a predictive dual-stage neural framework for phase-coherent auditory synthesis under non-stationary acoustic conditions. The framework decouples real-time carrier estimation from phase-coherent signal generation through two specialized modules. An intelligent acoustic sensing module (AI-1) estimates time-varying carrier information across harmonic, fluctuating, and broadband acoustic profiles using a causal neural front-end with an adaptive confidence-driven strategy. A predictive phase-coherent generator (AI-2) then forecasts short-horizon carrier trajectories and drives a discrete-time phase accumulator to maintain continuous phase evolution during binaural beat embedding. Objective evaluation under multiple acoustic profiles and noise conditions shows that the proposed framework maintains strong phase continuity, with a Phase Coherence Factor greater than 0.91, and low artifact levels, with a Signal-to-Artifact Ratio greater than 39.8 dB, under the evaluated conditions. Additional comparisons with conventional DSP baselines, stronger classical F0 estimators, a lightweight neural F0 tracker, and component-wise ablation variants further demonstrate that the performance improvement arises from the combination of adaptive carrier estimation and predictive phase-coherent actuation, rather than from carrier estimation alone. Hardware profiling shows a combined INT8 inference time of 2.4 ms per frame on a resource-constrained Raspberry Pi Zero 2W-class edge device. Importantly, this inference time and the sub-millisecond phase-accumulator resolution should not be interpreted as sub-millisecond end-to-end physical audio latency. The complete system still includes buffering, framing, neural inference, and output processing delay; the proposed method instead reduces effective phase-boundary misalignment through short-horizon predictive compensation. These results support the proposed framework as a lightweight engineering solution for real-time phase-continuous auditory synthesis in dynamic listening environments. The reported PCF and SAR values should be interpreted as signal-level indicators of phase continuity and artifact suppression, rather than as evidence of listener comfort, perceptual preference, or neurophysiological efficacy. Full article

Background/Objectives: This paper describes the synthesis of silica nanoparticles (SiNPs) and their surface modification with amino and phosphate groups (SiNPs-NH₂-PO₃). The functionalized nanoparticles were subsequently loaded with the anticancer drug 5-fluorouracil (SiNPs-NH₂-PO₃-5-FLU) and further modified with PEG2000 (SiNPs-NH₂-PO₃-5-FLU-PEG2000). Methods: In this study, a one-step, two-phase, sol–gel method carried out at room temperature was used to synthesize the nanoparticles. The size and surface zeta potential of the created SiNPs were determined by DLS measurements. HPLC was used to determine the amount of drug loaded into silica nanoparticles and the drug release profile in two different pH environments (slightly acidic and physiological). Based on physicochemical characteristics, the SiNPs-NH₂-PO₃-5-FLU and SiNPs-NH₂-PO₃-5-FLU-PEG2000 formulations were chosen for comprehensive characterization. The cytotoxicity of the studied complexes was assessed in MCF7 breast cancer cells, while their ability to induce apoptosis in those cells was examined using specific immunofluorescence markers: active caspase-7, active poly(ADP-ribose) polymerase (PARP), and p53 protein. Results: Our findings demonstrate that SiNPs-NH₂-PO₃-5-FLU can induce a stronger apoptotic response than free 5-FLU at equivalent concentrations. We observed that drug release occurs not only under physiological conditions but is further enhanced in a mildly acidic environment (pH 5.0), characteristic of the tumor microenvironment. Conclusions: Most 5-fluorouracil formulations are administered as injectable solutions, resulting in systemic exposure and significant adverse effects. However, their encapsulation within nanoparticles could favor preferential drug release in the acidic tumor microenvironment, thus supporting targeted therapy and reducing toxicity to healthy tissues. Moreover, PEGylation of the nanoformulation allows prolonged and controlled release. Full article

Sustainable management of industrial solid waste is critical for a circular economy. This study presents a novel approach for valorizing blast furnace slag (BFS) into NaA zeolite through selective acetic acid leaching followed by hydrothermal crystallization. The leaching step selectively extracts Ca²⁺ and Mg²⁺ while efficiently retaining silicon and aluminum in the solid residue, producing a reactive aluminosilicate precursor that facilitates zeolite nucleation and growth. The effects of the silicon-to-aluminum molar ratio (n(Si)/n(Al)), crystallization temperature, and duration on the phase evolution and morphology were systematically investigated. The results demonstrate that phase-pure NaA zeolite with high crystallinity and a uniform cubic morphology can be obtained from precursor gels with n(Si)/n(Al) ratios of 0.5–1.25. Optimal synthesis conditions were identified as n(Na):n(Si):n(Al):n(H₂O) = 6:1:1:240 at 373 K for 8 h. The resulting zeolites exhibit a BET specific surface area of 52.1 m²/g, a micropore volume of 0.016 cm³/g, an average adsorption pore size of 4.7 nm, and an external specific surface area of 12.8 m²/g. It achieved near-complete removal of Cu²⁺ and high adsorption efficiencies for Pb²⁺ (77.78%) and Ni²⁺ (71.79%) from 250 mg/L solutions at 298 K with a dosage of 4.0 g/L, following the affinity sequence Cu²⁺ > Pb²⁺ > Ni²⁺, with all pairwise differences statistically significant at p < 0.001, using one-way ANOVA and Tukey’s HSD tests. The adsorption of three metal ions was most accurately described by the Freundlich isotherm and pseudo-second-order kinetic models, indicating heterogeneous multilayer chemisorption. The theoretical maximum monolayer adsorption capacities (q_max) were 307.67 mg/g for Cu²⁺, 246.09 mg/g for Pb²⁺, and 173.79 mg/g for Ni²⁺, whereas the kinetic equilibrium adsorption capacities (q_e) reached 62.69, 48.85 and 41.69 mg/g, respectively. This study demonstrates a value-added strategy for valorizing BFS into a micro-mesoporous adsorbent, advancing both circular resource utilization and environmental remediation. Full article

Ultra-high-temperature ceramics (UHTCs) in the Ta–Hf–C ternary system are of significant interest for extreme aerospace and energy applications due to their melting points near 4000 °C. However, their synthesis typically requires extreme temperatures and pressures. This study reports a pectin-assisted low-temperature route for Ta-rich Ta_xHf_1−xC powder synthesis via carbothermal reduction at 1500 °C. The effect of Ta/Hf molar ratios (2.7/1, 0.9/1, and 0.3/1) on phase evolution, crystallinity, and morphology was systematically investigated. FTIR confirmed the successful formation of homogeneous hybrid organic–inorganic precursors through the chelation of metal ions with pectin functional groups. XRD results demonstrated that the Ta-rich composition (Ta/Hf = 2.7/1) promotes the formation of a high-purity (95.87%) cubic solid solution (lattice parameter a = 4.453 Å) with sharp reflections and improved crystallinity. In contrast, Hf-rich samples exhibited incomplete conversion, leaving unreacted HfO₂ and Ta₂Hf₆O₁₇ oxide phases due to the high thermodynamic stability of hafnia. Microstructural analysis revealed quasi-spherical Ta_xHf_1−xC particles with an average size of approximately 123 nm, together with finer residual oxide particles of about 50 nm. Overall, these results demonstrate that pectin-assisted precursor chemistry is an effective strategy for promoting low-temperature carbide formation in Ta-rich Ta_xHf_1−xC compositions. Full article

Background: Multi-objective optimization (MOO) is widely used in engineering design and energy systems to represent trade-offs through Pareto fronts. Yet practical deployment requires moving from a non-dominated set to an implementable preferred design, and this decision step is often treated implicitly. Many studies equate decision support with improved Pareto front generation or visualization, while decision-maker preferences are assumed, weakly specified, or not elicited from stakeholders. Methods: A two-phase scoping evidence synthesis with PRISMA-informed reporting was adopted to map the literature and synthesize explicit Pareto-front decision-support mechanisms. Phase 1 produced a broad evidence map of how Pareto-front decision support is framed and clustered studies by primary contribution, while Phase 2 conducted a focused synthesis of explicit Pareto-front decision-support methods using refined searches in Scopus and SpringerLink. Results: Phase 1 mapped 46 studies; only 10 reported an explicit reproducible Pareto front solution-selection mechanism. Phase 2 included 17 studies and identified four method families: post hoc scoring and ranking, compromise aggregation, interactive preference-guided exploration, and preference elicitation and learning. Conclusions: The literature remains dominated by Pareto front generation and exploration rather than reproducible final solution selection; future work should strengthen preference elicitation, transparency, sensitivity analysis, and uncertainty-aware recommendation stability. 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