Search Results (232)

Life could not emerge through molecular synthesis alone; it also required mechanisms that coupled environmental energy to directional chemical change. Yet, ATP, the dominant energy carrier in modern cells, depends on nucleotide synthesis, selective catalysis, and membrane-based regeneration, making it an unlikely starting point for bioenergetics. Here, I examine inorganic pyrophosphate as a possible intermediate between geochemical phosphate activation and ATP-centred metabolism. Condensed phosphates can form under plausible volcanic, mineral-mediated, and wet–dry conditions, and pyrophosphate has sufficient transfer potential to support selected phosphorylation reactions and ion translocation when appropriately coupled. I propose that recurrent pyrophosphate production could have promoted the formation of phosphorylated sugars, linking prebiotic carbon synthesis to non-enzymatic reaction networks resembling central metabolism. Activated enol and acyl phosphates may subsequently have regenerated pyrophosphate, allowing partial energetic closure. I further consider how polyphosphorylated pentoses could have provided transitional group-transfer scaffolds from which nucleotide-based activation chemistry emerged. In this view, ATP did not replace an unrelated primordial currency, but consolidated functions already distributed across simpler phosphate compounds. The persistence of pyrophosphate in biosynthetic directionality, phosphoryl transfer, and membrane energetics may therefore reflect a remnant of an earlier energetic architecture. Full article

Background: The optical losses in the form of reflections, parasitic absorption, and scattering limit photovoltaic efficiency. This review examines plasma-assisted surface engineering as an effective tool for improving light management in solar cells. Plasma-based methods, including etching, oxidation, deposition, and texturing, enable precise control of surface morphology and chemistry, lowering reflectance, enhancing light trapping, and passivating defects. Methods: In contrast to wet-chemical or high-temperature processes, plasma processes are dry, low-temperature, scalable, and can be used with silicon, perovskite, thin-film, and organic solar cells, as well as tandem structures. The fundamentals of optical losses are described, along with the principles of radio-frequency (RF), inductively coupled plasma (ICP), microwave, and atmospheric plasma systems and their distinctive advantages for controlling ion and reactive-species generation. Key applications reviewed include black-silicon texturing by ICP reactive-ion etching (ICP-RIE), anti-reflective/passivation coatings by plasma-enhanced chemical vapor deposition (PECVD), and interface activation by atmospheric plasma. Results: Among performance improvements are a reflectance of less than 2%, a photocurrent increase of 10–20%, and longer carrier lifetime. Conclusions: The advantages of plasma compared to lithography and sol–gel processes are in the precision and affordability of the method. The difficulties include damage caused by the processing, uniformity over extensive areas, and environmental stress resistance. Future directions rely on low-temperature plasmas for flexible PV, machine-learning-guided process optimization, and hybrid plasma–laser systems. This synthesis of otherwise fragmented studies is intended to support the implementation of plasma-based methods in next-generation, high-efficiency, and sustainable solar production. Full article

The modulation of ZnO physicochemical properties through Mn doping represents a promising strategy for the development of multifunctional nanomaterials with enhanced biological performance. In this study, we investigate how the nominal Mn concentration influences both the physicochemical properties and antibacterial, antibiofilm, and anti-virulence activities of ZnO nanoparticles (NPs). Mn-doped ZnO nanoparticles containing nominal Mn from 2.5 to 10 mol% were synthesized through a simple wet-chemical approach and characterized by UV–Vis, Raman, TEM, EDX, and EELS analyses. The resulting ZnO-based NPs showed average dimensions of 3.7–4.8 nm, while increasing Mn incorporation produced measurable changes in optical response and morphology of nanoparticles. Antibacterial activity was evaluated against Gram-positive and Gram-negative bacterial models by assessing planktonic growth inhibition, biofilm formation, and pyocyanin production. The sample with the highest Mn amount (Mn₁₀-ZnO) markedly enhanced antibacterial performance by reducing MIC₉₀ from 150 to 37.5 μg/mL against Staphylococcus aureus and from 300 to 75 μg/mL for Pseudomonas aeruginosa. Mn doping also enhanced biofilm inhibition and produced a progressive reduction in pyocyanin synthesis. These results establish a concentration-dependent relationship between Mn concentration, nanoparticle properties, and antibacterial performance, highlighting the potential of Mn-doped ZnO nanoparticles for the development of anti-infective biomaterials, including antimicrobial coatings for implantable medical devices. Full article

Plasma–liquid interactions (PLIs) have emerged as a rapid and reagent-minimized platform for the synthesis of gold nanomaterials (GNMs) with tunable size, morphology, crystallinity, and surface chemistry. In contrast to conventional wet-chemical routes, non-thermal atmospheric-pressure plasmas reduce HAuCl₄ through highly reactive species generated at the gas–liquid interface. This review consolidates the field by classifying PLIs systems into four categories based on the discharge configuration, including plasma electrochemistry, plasma jet, solution plasma, and plasma aerosol, and critically compares their mechanisms and operational parameters. We show that the relative weighting of key process variables is strongly configuration-specific, with short-lived species initiating burst nucleation and long-lived neutrals sustaining autocatalytic growth. Furthermore, the review highlights how the distinct characteristics of each PLI configuration affect nanoparticle formation, morphology evolution, and physicochemical properties, providing practical guidance for selecting appropriate plasma systems for the controlled synthesis of gold nanomaterials. Full article

This study investigates the synthesis of La_0.6Ca_0.4FeO₃ (LCF) perovskite via a ball milling method for application in reverse water–gas shift chemical looping (RWGS-CL) for CO₂-to-CO conversion. Unlike conventional wet-chemical routes such as the Pechini method, the ball milling approach offers a solvent-free, scalable synthesis using low-cost metal oxide precursors (e.g., La₂O₃, CaO, Fe₂O₃). Structural analysis by XRD confirmed the successful formation of single-phase cubic perovskite, with no secondary phases when using oxide precursors. Crystallite size increased with calcination temperature, from 118.9 Å (no calcination) to 404.3 Å (1050 °C). BET analysis revealed a decrease in surface area from 2.5 m²/g (no calcination) to 0.51 m²/g (1050 °C), consistent with sintering at higher temperatures. TPR-H₂ and TPO-CO₂ studies revealed that non-calcined LCF possesses slightly enhanced redox properties, with oxygen vacancy formation and CO₂ reoxidation activity both at 500 °C. RWGS-CL experiments demonstrate that all LCF samples exhibit stable CO production (910–970 µmol/g_LCF) over multiple cycles at 500 °C, with comparable performance across calcination conditions. A cost and sensitivity analysis reveals that the ball milling method had lower synthesis costs by approximately 92% at the laboratory-scale and 88% at the industrial-scale compared to the Pechini method, highlighting its strong potential for large-scale perovskite production. Full article

Silicon carbide (SiC) nanowires possess unique one-dimensional structural features, excellent mechanical strength, thermal stability and wide bandgap properties, showing great potential in high-temperature electronics, catalysis, sensing and composite reinforcement. Nevertheless, pristine SiC nanowires suffer from inert surface activity, weak interfacial compatibility and limited optoelectronic and catalytic performance. Surface coating and heterojunction engineering are effective strategies to address these deficiencies. This review systematically summarizes the synthesis routes of pristine SiC nanowires, including carbothermal reduction, chemical vapor deposition, template-assisted growth and molten salt synthesis, as well as their morphological regulation, physicochemical properties and inherent limitations. Meanwhile, typical coating methods such as wet chemical, hydrothermal, CVD and PIP are elaborated, and the influences of coating thickness, uniformity, adhesion and lattice/thermal compatibility on performance are summarized. The classification and interfacial charge mechanism of Type II, Z-scheme and Schottky heterojunctions are discussed, and the advances of coated SiC nanowires in photodetection, photocatalysis, gas sensing, electromagnetic shielding and energy storage are reviewed. Current challenges including coating stability, scalable preparation and integration bottlenecks are pointed out, and future research directions focusing on interface control, multifunctional integration and AI-assisted material design are prospected. Full article

High-entropy alloys (HEAs), composed of five or more principal elements in near-equimolar ratios, have emerged as a groundbreaking class of materials for next-generation flexible electronics. This review systematically examines the unique potential of HEAs as sensing materials, moving beyond their traditional role as structural components. We first elucidate the fundamental mechanisms—core effects including lattice distortion, sluggish diffusion, and the cocktail effect—that endow HEAs with an exceptional synergy of high strength, good ductility, tunable electrical resistivity, and superior electrocatalytic activity. Subsequently, we critically analyze the state-of-the-art strategies for processing HEA-based micro/nano structures, including mechanical alloying, wet-chemical synthesis, and non-equilibrium deposition techniques, with an emphasis on their compatibility with flexible substrates. The core of the review categorizes and discusses the latest advances in HEA-based flexible sensors for strain/stress, gas, and electrochemical (e.g., glucose, biomarkers, heavy metals) detection, highlighting the structure–property–performance relationships. Representative studies have demonstrated that HEA flexible strain sensors achieve a temperature coefficient of resistance as low as 45.59 ppm/K with no signal drift over 6000 stretching cycles; room-temperature hydrogen sensors reach a detection limit down to 31 ppb with a response time of 19 s; and non-enzymatic glucose sensors deliver a sensitivity up to 3043 μA·mM⁻¹·cm⁻². Finally, we summarize the key challenges—such as manufacturing scalability, long-term stability under dynamic deformation, and cost-effectiveness—and provide a forward-looking perspective on promising research directions, including high-throughput compositional screening, multi-functional sensor arrays, and the integration of machine learning for rational material design. 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

To mitigate health hazards from pathogenic bacteria (Escherichia coli, Staphylococcus aureus) and fungi (Aspergillus niger) as well as the coating mildew issue in high-humidity indoor environments, and to overcome the challenges of particle agglomeration and non-uniform distribution in conventional benzalkonium chloride (BAC)-clay composites, this study proposes a wet chemical strategy to prepare BAC-hectorite antimicrobial composites using synthetic hectorite as a high-performance carrier, which is superior to natural clays such as montmorillonite and kaolin in structural uniformity, ion-exchange efficiency, and dispersion stability. Characterization using X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and Brunauer–Emmett–Teller (BET) analysis confirmed the successful intercalation of BAC cations into the hectorite interlayers through ion exchange. This resulted in a significant expansion of the interlayer spacing from 1.0–1.2 nm to 1.5–1.8 nm, a marked alleviation of particle agglomeration, and an optimized pore structure. A clear structure–activity relationship between preparation conditions, microstructure regulation, and antimicrobial performance is systematically established. Antibacterial tests revealed superior efficacy against Gram-positive bacteria; the composite exhibited an inhibition zone of 13.31 mm and a minimum inhibitory concentration (MIC) of 4 μg/mL against S. aureus, compared to 11.62 mm and 32 μg/mL against E. coli. Practical application tests demonstrated that at an ultralow addition level of 0.4%, incorporating this composite into latex paint achieved an antibacterial rate exceeding 99.9% against both pathogens. When added to putty powder, it yielded Grade 0 mold resistance with no observable growth. Furthermore, compounding with polypropylene (PP) increased the elongation at break to approximately 600%, simultaneously realizing antibacterial, antifungal, and toughening functions, thereby not only conferring antibacterial functionality but also significantly enhancing toughness—resolving the typical polymer embrittlement caused by traditional inorganic antibacterial fillers. Short-term evaluations confirm that this composite offers a stable structure, high-efficiency antimicrobial properties, and improved substrate mechanics at low loading levels. These findings provide technical support and experimental guidance for the functional upgrading of indoor decorative coatings, putties, and polymer materials used in high-humidity scenarios such as kitchens and bathrooms. Full article

Bone tissue has a remarkable regenerative capacity; however, advanced strategies are needed to support the repair process for critical-sized defects. While autografts and allografts remain the gold standard, their limitations have stimulated alternative approaches in bone tissue engineering, in search of scaffolds capable of mimicking native bone properties to promote effective regeneration. In this study, silk fibroin (SF)-based composite scaffolds incorporating β-tricalcium phosphate (β-TCP) and poly-ε-caprolactone (PCL) were synthesized using a simple and innovative cryogenic foaming method. The proposed fabrication technique overcomes many limitations of current synthesis methods, such as long processing times, the use of solvents, and reliance on complex, energy-intensive equipment. The composites were characterized using infrared spectroscopy to confirm the incorporation of all three components and their chemical bond arrangements. µ-CT, SEM, and ESEM analyses revealed that SF/β-TCP/PCL scaffolds exhibited great porosity and dynamic interaction with water while preserving pore morphology in wet environments. Swelling behavior, indirect cytotoxicity, and cell proliferation tests recognized the greater performance of SF/β-TCP/PCL scaffolds in promoting long-term cell proliferation, maintaining superior mechanical properties. These findings indicate that the proposed original, simple, and relatively low-cost manufacturing approach enabled the fabrication of scaffolds with excellent mechanical performances, controlled and stable porosity under both dry and physiological-like conditions, and high biocompatibility. The resulting constructs demonstrated promising results for cell proliferation and osteoconductive behavior, supporting their potential suitability as artificial bone substitutes. Full article

Red mud discharged during alumina production via the Bayer process is characterized by high contents of sodium carbonate, sodium sulfate, and other soluble salts, and it remains poorly utilized and accumulates in long-term stockpiles. Sodium percarbonate has found extensive industrial applications, and its synthesis via the salting-out method represents one of the dominant industrial routes. In this context, sodium sulfate was employed as a salting-out agent. On the basis of relevant ternary systems, the phase equilibrium of the quaternary system Na₂CO₃–Na₂SO₄–H₂O₂–H₂O at 5 °C was systematically investigated and calculated. The objective was to utilize red mud as a waste resource and develop a novel integrated process that favored the wet synthesis of sodium percarbonate while enabling the efficient separation of sodium salts. The solubility data for the ternary subsystems constituting the above quaternary system were correlated using the Pitzer model, yielding the corresponding ion interaction parameters and activity coefficients. The validated model was then applied to predict the phase equilibrium data of the quaternary system. Verification results indicate that the calculated values are in satisfactory agreement with the experimental data. On the basis of the phase equilibrium data of the Na₂CO₃–Na₂SO₄–H₂O₂–H₂O system at 5 °C, a phase diagram was constructed. Along with five solid-phase crystallization fields, three invariant points were identified: the co-saturation point of Na₂SO₄·10H₂O, Na₂CO₃·10H₂O, and Na₂CO₃·1.5H₂O₂·H₂O; the co-saturation point of Na₂SO₄·10H₂O, Na₂CO₃·1.5H₂O₂·H₂O, and Na₂SO₄·0.5H₂O₂·H₂O; and the co-saturation point of Na₂CO₃·1.5H₂O₂·H₂O, Na₂SO₄·0.5H₂O₂·H₂O, and Na₂CO₃·2H₂O₂·H₂O. From phase diagram analysis, a novel wet process route for sodium percarbonate production using waste red mud is proposed. The process involves chemical reaction, crystallization, separation, and drying to obtain the final product. A new process flow diagram for the value-added production of sodium percarbonate is also presented. Full article

Dopamine (DA) is a crucial catecholamine neurotransmitter, and its abnormal levels are closely associated with neurological disorders such as Parkinson’s disease. Electrochemical sensing technology offers a rapid and cost-effective platform for DA detection; however, it often suffers from interference from coexisting biomolecules such as ascorbic acid (AA) and uric acid (UA). In this study, we report a novel electrochemical biosensor based on PdMo bimetallene, a nanomaterial synthesized via a facile wet-chemical approach, aiming to enhance the detection performance and selectivity for DA. PdMo bimetallene is a highly curved, atomically thin two-dimensional nanosheet featuring abundant strained sites and a high density of active centers, enabling the selective and sensitive detection of DA. The results demonstrate that the as-prepared PdMo bimetallene-modified glassy carbon electrode (GCE) exhibits excellent electrocatalytic activity toward the oxidation of DA. The sensor displays a good linear response over the concentration range from 10 nM to 200 µM, with an ultrahigh sensitivity of 80 µA·µM⁻¹ cm⁻² and a low detection limit of 0.14 µM (S/N = 3). Owing to the synergistic electronic effect between Pd and Mo, the high density of exposed active sites, and the unique strained lattice structure of the bimetallene, the sensor enables accurate determination of DA concentrations even in the presence of interfering species such as AA and UA. In summary, the successfully fabricated PdMo bimetallene-based sensor offers the advantages of low cost, facile synthesis, a wide linear range, and high sensitivity, positioning it as a promising candidate for neurotransmitter detection applications. Full article

High-entropy alloys (HEAs) are typically produced using high-temperature metallurgical routes; however, alternative synthesis approaches based on wet-chemical processing remain relatively unexplored. In this study, a compositionally complex two-phase AgCuCoNiFe high-entropy alloy was synthesized using a precipitation–reduction strategy involving co-precipitation of mixed metal carbonates followed by thermal reduction in a reducing atmosphere. The objective of the work was to evaluate the feasibility of this hydrometallurgical route for preparing compositionally complex alloys and to investigate the structural evolution of the material as a function of reduction time. Quantitative MP-AES analysis confirmed efficient co-precipitation of all five elements, enabling the preparation of a precursor with near-equimolar metal composition. Structural characterization using SEM, EDS, and XRD revealed the presence of surface compositional heterogeneity in the as-reduced state, characterized by Ag-enriched domains. After controlled surface abrasion, the internal material exhibited significantly more uniform elemental distribution, although the obtained composition was not equimolar. X-ray diffraction patterns showed a transition from multiple sharp reflections at the surface to broadened peaks in the bulk, consistent with enhanced alloying within the bulk compared to the surface, while still revealing a two-phase character. Microhardness measurements indicated moderate hardness with mean values in the range of 187–221 HV with no significant dependence on reduction time, while wettability analysis revealed moderately hydrophilic behavior with contact angles in the range of approximately 75–83°. The results suggest that precipitation–reduction can be a viable alternative route for the synthesis of multicomponent HEAs, enabling the formation of chemically mixed alloy structures without the use of conventional melting-based processing. However, the obtained alloy exhibits incomplete chemical homogeneity, indicating that further optimization of the synthesis conditions is required to achieve a fully uniform composition. Full article

In the present paper, In₂O₃ NPs were synthesized by a wet-chemical method, in the absence and presence of the surfactant, and deposited as thin films on silicon substrates. After deposition, the films were subjected to rapid thermal annealing (RTA) at 550 °C, 750 °C, and 900 °C, for 300 s, under an inert atmosphere. The correlation between the morphological, structural, and optical characteristics, the wetting capacity of In₂O₃ films synthesized under different synthesis conditions, and the influence of the RTA treatment are presented. The vibrations of In-O bonds for In₂O₃ samples were confirmed using FTIR spectroscopy. Structural analysis shows that In₂O₃ NPs have a cubic crystalline structure, but with the increase in temperature at 900 °C, diffraction peaks characteristic of the tetragonal phase of indium appear, correlated with a decrease in lattice parameters, as a result of the crystallinity. The morphology of the In₂O₃ samples was studied by SEM, revealing predominantly spherical and uniformly distributed particles with nanometric sizes. The absorption spectra of the In₂O₃ NPs showed peaks in the ultraviolet region, and the high energy bandgap value of the In₂O₃ films varied between 3.28 and 4.33 eV, depending on the samples and RTA treatment. The contact angle measurements of In₂O₃ films determined the wetting capacity of the surface, reflecting changes in surface morphology and structure induced by the RTA process. The results suggest that In₂O₃ thin films with spherical nanoparticles, good wettability, and percolation can be used for the development of sensors with increased selectivity and sensitivity. Full article

Layered sodium transition-metal oxides are promising cathode materials for sodium-ion batteries due to their high theoretical capacity; however, their practical application is often limited by sluggish Na⁺ diffusion kinetics and structural instability during cycling. P2/O3 phase coexistence has been proposed as an effective strategy to balance capacity and stability, yet it is typically achieved through precise Na-content tuning or complex synthesis conditions, which restrict compositional flexibility. Herein, we demonstrate a phase-engineering approach that induces stable P2/O3 phase coexistence without adjusting the overall Na stoichiometry by controlling the dopant incorporation pathway. Using Na_0.8(Ni_0.25Fe_0.33Mn_0.33Cu_0.07)O₂ (NaNFMC) as a model system, Mg doping via a wet chemical route enables homogeneous dopant distribution, which triggers local stacking rearrangement and the formation of prismatic Na⁺ diffusion channels characteristic of the P2 phase. In contrast, dry-doped samples with identical Mg content retain a predominantly O3-type structure, highlighting the decisive role of dopant incorporation in governing phase evolution. As a result of the phase-engineered P2/O3 coexisting framework, the Mg wet-doped cathode exhibits enhanced initial reversibility, superior rate capability, and improved long-term cycling stability compared to pristine and dry-doped counterparts. Voltage-resolved dQ/dV and cyclic voltammetry analyses reveal stabilized redox behavior with reduced polarization, while electrochemical impedance spectroscopy confirms suppressed impedance growth and improved Na⁺ transport kinetics after cycling. This study establishes that phase engineering through controlled dopant incorporation provides an effective alternative to conventional Na-content tuning strategies for layered sodium cathodes. The findings offer a scalable and versatile design principle for optimizing the electrochemical performance and structural durability of next-generation sodium-ion battery cathode materials. Full article