Search Results (1,097)

Cesium halide perovskite nanocrystals (PNCs) have emerged as promising materials for application in high-color-purity displays due to their exceptional optoelectronic properties, which include narrow emission linewidths, tunable bandgaps, and high photoluminescence quantum yields (PLQYs). However, preserving these characteristics during purification remains a major challenge as surface ligand detachment during the washing process can lead to increased defect states, reduced quantum efficiency, and spectral broadening. The choice of anti-solvent plays a crucial role in maintaining the structural and optical integrity of PNCs, as it directly influences ligand retention and material stability. In this study, we propose an optimized purification strategy for mixed-halide perovskite nanocrystals that incorporates post-synthetic ligand supplementation, in which controlled amounts of oleic acid (OA) and oleylamine (OAm) are sequentially introduced into the crude solution prior to anti-solvent treatment. This approach reinforces surface passivation, suppresses trap state formation, and minimizes halide loss. Consequently, a near-unity PLQY with narrow full-width-at-half-maximum emissions is achieved for both green- and red-emissive nanocrystals, markedly enhancing color purity and providing a promising route toward next-generation wide-color-gamut display technologies. Full article

The global reliance on fossil fuels has caused severe environmental challenges, emphasizing the urgent need for sustainable and renewable energy sources. Bioethanol production from lignocellulosic biomass has emerged as a promising alternative due to its abundance, renewability, and carbon-neutral footprint. However, its economic feasibility remains a major obstacle owing to high production costs, particularly those associated with low ethanol titers and the energy-intensive distillation process costs for low titers. High-solid loading processes (≥15% w/w or w/v) have demonstrated potential to overcome these limitations by minimizing water and solvent consumption, enhancing sugar concentrations, increasing ethanol titers, and lowering downstream processing cost. Nevertheless, high-solid loading also introduces operational bottlenecks, such as elevated viscosity, poor mixing, and limited mass and heat transfer, which hinder enzymatic hydrolysis efficiency. This review critically examines emerging pretreatment and enzymatic hydrolysis strategies tailored for high-solid loading conditions. It also explores techniques that improve sugar yields and conversion efficiency while addressing key technical barriers, including enzyme engineering, process integration, and optimization. By evaluating these challenges and potential mitigation strategies, this review provides actionable insights to intensify lignocellulosic ethanol production and advance the development of scalable, cost-effective biorefinery platforms. Full article

Two-dimensional (2D) colloidal CsPbBr₃ nanosheets (NSs) possess size-dependent optoelectronic properties; however, conventional hot-injection methods often lack precise growth control and well-ordered superlattice self-assembly. Herein, we introduce a modified ligand-assisted hot-injection strategy that promotes direct precursor–ligand interactions prior to solvent mixing, thereby enabling highly controlled nanosheet superlattice growth. By adjusting the reaction temperature from 130 to 150 °C, we obtained rectangular nanosheets with monodisperse, well-defined thicknesses of 3.35 ± 0.05 nm and 4.05 ± 0.09 nm at 130 and 140 °C, respectively, both below the 7 nm exciton Bohr diameter, consistent with strong quantum confinement. The resulting superlattices exhibited sharp, tunable photoluminescence peaks at 462, 464, and 513 nm, with time-resolved PL revealing a clear size–lifetime correlation, where smaller lateral superlattices at 130 °C showed a short decay time of 8.65 ns, intermediate growth at 140 °C yielded 15.42 ns, and larger lateral superlattices at 150 °C reached 35.49 ns. Importantly, the modified synthesis facilitated the formation of ordered superlattices that preserved their intrinsic emission properties, underscoring their structural stability and scalability. These findings establish a direct link between ligand-mediated synthesis, reaction temperature, nanosheet dimensions, and optical performance, offering a pathway to high-quality perovskite NS superlattices for advanced optoelectronic applications such as light-emitting diodes and sensors. Full article

New compostable materials have been developed to replace single-use soft materials such as polyurethane foams (PUR). To this end, eco-friendly systems have been formulated on the basis of agar gels prepared in mixed solvent (glycerol/water) to meet specifications, i.e., stiffness of several hundred kPa, reasonable extensibility, and good stability when exposed to open air. While the addition of glycerol slows down gelation kinetics, mechanical properties are improved up to a glycerol content of 80 wt%, with enhanced extensibility of the gels while maintaining high Young’s moduli. Swelling analyses of mixed gels, in water or pure glycerol, demonstrate the preservation of an energetic network, with no change in volume, in pure water and the transition towards an entropic network in glycerol related to the partial dissociation of helix bundles. Dimensional and mechanical analysis of gels aged in an open atmosphere at room temperature shows that the hygroscopic character of glycerol enables sufficient water retention to maintain the physical network, with antagonistic effects linked to relative increases in glycerol, which tends to weaken the network, and agar, which on the contrary strengthens it. Complementary analyses carried out on aged agar gels formulated with an initial glycerol/water mass composition of 60/40, the most suitable for the targeted development, enabled the comparison of the properties of agar gels favorably with those of PURs and verified their stability during long-term storage, as well as their non-toxicity and compostability. Full article

Electrospun fibers serve as a medium for the targeted release of active compounds, facilitating the desired therapeutic effects in drug administration. The point of this study was to find the best conditions for making electrospun fibers from cellulose acetate (CA) and poly(ε-caprolactone) (PCL), mixed with pure oxyresveratrol extract from Artrocarpus lakoocha Roxberg (Moraceae). Additionally, the study focused on evaluating the antioxidant properties, antityrosinase activity, and freeze–thaw stability of the resulting fibers. We incorporated a concentration of oxyresveratrol at 0.1% w/w into various mass ratios of CA/PCL blended fiber sheets (1:0, 3:1, 1:1, 1:3), utilizing mixed solvents of acetone/DMF (2:1% v/v) and chloroform/DMF (9:1% v/v) for preparation. The fiber sheets displayed a continuous and uniform structure, with fiber diameters ranging from 300 to 1000 nanometers. We investigated the release kinetics of oxyresveratrol from the fibrous substrates using the total immersion technique, specifically in phosphate-buffered saline at a pH of 7.4. The results showed that the fiber sheet with a 3:1 w/w ratio of CA to PCL and a 0.1 w/w loading of oxyresveratrol showed the most significant release of oxyresveratrol at the 2 h mark, and it continued to release consistently at this peak value for up to 24 h. The antioxidant and anti-tyrosinase properties of oxyresveratrol in fiber sheets were more stable than those of free oxyresveratrol at the same concentrations. The fiber sheet presents a promising avenue for a user-friendly transdermal patch application. Full article

Potholes are typical scattered distresses on asphalt pavements, severely impairing traffic safety and pedestrian safety due to delayed repair time and secondary distress. Aiming to extend the service life of repaired potholes, this study develops a pothole repair technique characterized by repair materials with superior performance and adhesive materials with high bonding strength. Firstly, the mechanical analysis for repaired potholes was conducted via finite element simulation, and thereafter, corresponding technical measures were derived to prevent the recurrence of distress in repaired potholes. Secondly, according to the material composition of solvent-based cold-mix asphalt (SCMA) and emulsified-based cold-mix asphalt (ECMA), pavement performance testing methods were proposed to test and evaluate their forming strength, high-temperature stability, low-temperature crack resistance, and water stability. On this basis, interlayer shear tests, pull-out tests, and field pothole repair cases with varying repair materials and adhesive materials were conducted, and the interfacial bonding strengths with the old pavement were then compared to optimize the pothole re-pair technique. The results showed that (1) increasing the repair material modulus and interfacial friction coefficient reduces the pressure strain (σ_y) and pressure stress (ε_y), thereby decreasing the risk of secondary dis-tress; (2) ECMA exhibits superior pavement performance, with strength and rutting resistance 49.7%–64.6% higher than SCMA; (3) the combination of ECMA and WER-EA achieves the highest interfacial pull-out and shear strengths, with their values 76.7%–78.2% higher than SCMA+WER-EA); and (4) after 1 year of opening to traffic, potholes repaired with ECMA+WER-EA show minimal thickness loss of 0.2 cm and no aggregate peeling at the edges, thus being recommended as the optimal solution for repairing potholes. This study clarifies the secondary distress mechanism of repaired potholes and provides an optimal repair scheme (ECMA+WER-EA) for engineering applications. Full article

Natural Deep Eutectic Solvents (NADES) were synthesized from food-grade components and evaluated as green extractants for the simultaneous recovery and liquid chromatography coupled to quadrupole-Orbitrap mass spectrometry (LC–Q-Orbitrap-MS) analysis of biopesticide residues in a complex matrix like honey. Conventional solid–liquid extraction (SLE) was applied, initially using choline chloride-2,3-butanediol (1:4, molar ratio) as the NADES extractant solvent, before systematically evaluating other NADES formulations. Extraction parameters, such as time (10 min, 20 min, and 30 min), technique (rotary mixing vs. sonication), and NADES composition, namely lactic acid–glucose–water (LGH, 5:1:9, molar ratio), lactic acid–glycerol–water (LGLH, 1:1:3, molar ratio), urea–glycerol–water (UGLH, 1:1:2, molar ratio), and choline chloride–2,3-butanediol (ChClBt, 1:4, molar ratio), were systematically optimized. Rotating agitation for 10 min yielded the highest overall recoveries and was therefore selected as the optimal extraction time. Rotary shaking was chosen over sonication due to its superior performance across both simple and complex matrices. Among the NADES tested, UGLH proved to be the most effective composition for the honey matrix. The analytical method was validated for the honey matrix. Linearity showed excellent performance across the tested concentration range, with R² values above 0.95 for all analytes. Matrix effects were within ±20% for nearly half of the compounds, while a few exhibited moderate matrix enhancement. Recoveries ranged from 50.1% to 120.5% at 500 µg/kg and 1000 µg/kg, demonstrating acceptable extraction performance. Intra-day and inter-day precision showed relative standard deviations (RSDs) below 20% for most analytes. Limits of quantification (LOQs) were established at 500 µg/kg for eight compounds based on recovery and precision criteria. These results confirm the suitability of the proposed NADES-based method for sensitive and reliable analysis of biopesticide residues in honey. When compared to conventional extraction methods, the proposed NADES-based protocol proved to be a greener alternative, achieving the highest AGREEprep score due to its use of non-toxic solvents, lower waste generation, and overall sustainability. Full article

The precipitation of cellulose and polyacrylonitrile and its copolymer (PAN) solutions is a well-known process that has been extensively described in numerous studies. It is suggested that “soft” precipitants (aqueous solutions of solvent, alcohols) be used in place of “rigid” ones (water) to control the rate at which solutions precipitate. Diffusion processes can also be controlled by lowering the temperature of the interacting system’s constituent parts. The appearance and structure of the resulting fibers (films) are directly correlated with the rate of coagulation. Adding a composite additive to the solution is an unusual method of altering the rate of polymer phase release. The introduced additive should dissolve in a common solvent, which will ensure the competition of precipitation between the polymer phases. It is shown that using optical methods it is possible to trace the evolution of the polymer phase precipitation and the formed morphology. For 12% solutions of cellulose, PAN and mixed systems in N-methylmorpholine-N-oxide (NMMO) the kinetics of the movement of isoconcentration planes was traced and the growth rates of the precipitated polymer zone were estimated. The introduction of PAN additives into cellulose enables the influence of diffusion processes and minimizes the formation of finger-like defects (vacuoles). When the PAN content in the system is 30% or more, the formation of defects in the precipitated solution is significantly suppressed, which is crucial for achieving a uniform morphology. Full article

Quasi-two-dimensional (Q2D) perovskite films have garnered significant attention as novel gain media for lasers due to their tunable bandgap, narrow linewidth, and solution processability. Q2D perovskites endowed with intrinsic quantum well structures demonstrate remarkable potential as gain media for cost-effective miniaturized lasers, owing to their superior ambient stability and enhanced photon confinement capabilities. However, the mixed-phase distribution within Q2D films constitutes a critical determinant of their optical properties, exhibiting pronounced sensitivity to specific fabrication protocols and processing parameters, including annealing temperature, duration, antisolvent volume, injection timing, and dosing rate. These factors frequently lead to broad phase distribution in Q2D perovskite films, thereby inducing incomplete exciton energy transfer and multiple emission peaks, while simultaneously making the fabrication processes intricate and reducing reproducibility. Here, we report a novel annealing-free and antisolvent-free method for the preparation of Q2D perovskite films fabricated in ambient atmosphere. By constructing a tailored mixed-solvent vapor atmosphere and systematically investigating its regulatory effects on the nucleation and growth processes of film via in situ photoluminescence spectra, we successfully achieved the fabrication of Q2D perovskite films with large n narrow phase distribution characteristics. Due to the reduced content of small n domains, the incomplete energy transfer from small n to large n phases and the carriers’ accumulation in small n can be greatly suppressed, thereby suppressing the trap-assistant nonradiative recombination and Auger recombination. Ultimately, the Q2D perovskite film showed a single emission peak at 519 nm with the narrow full width at half maximum (FWHM) of 21.5 nm and high photoluminescence quantum yield (PLQY) of 83%. And based on the optimized Q2D film, we achieved an amplified spontaneous emission (ASE) with a low threshold of 29 μJ·cm⁻², which was approximately 60% lower than the 69 μJ·cm⁻² of the control film. Full article

The inhibition mechanism and binding properties of four phenolic acids (ferulic acid (FA), p-coumaric acid (CA), gallic acid (GA), and protocatechuic acid (PA)) on xanthine oxidase (XOD) were investigated. All four phenolic acids acted via a mixed inhibition pattern, mainly influencing the hydrophobic regions and secondary conformation of XOD through hydrophobic bonding and hydrophobic association. Molecular dynamics simulations exhibited that the complexes of XOD with FA and CA revealed smaller radii of gyration (Rg) and solvent-accessible surface areas (SASA), along with lower variability in root-mean-square deviation (RMSD) and root-mean-square fluctuation (RMSF), collectively indicating greater structural stability. FA, CA, and PA significantly reduced uric acid (UA) concentration in the 25–100 μM range. Although GA only reduced UA levels in cell models at 25 μM, this effect was likely due to its larger polar surface area, which limits cellular uptake. Absorption, distribution, metabolism, excretion, and toxicity (ADMET) evaluation suggested that these phenolic acids have potential for development. Full article

Acrylonitrile–butadiene–styrene (ABS) has been widely used as an engineering thermoplastic, and the increasing post-consumer waste of ABS plastics calls for efficient and sustainable recycling technologies. The recent advances in ABS recycling technologies were investigated to enhance material recovery, purity, and environmental performance. Thermo-oxidative degradation compromises mechanical integrity during reprocessing, while minor reductions in molecular weight increase melt flow rates. Surface modification techniques such as boiling treatment, Fenton reaction, and microwave-assisted flotation facilitate the selective separation of ABS from mixed plastic waste by enhancing its hydrophilicity. Dissolution-based recycling using solvent and anti-solvent systems enables the recovery of high-purity ABS, though some additive losses may occur during subsequent molding. Magnetic levitation and triboelectrostatic separation provide innovative density and charge-based sorting mechanisms for multi-plastic mixtures. Thermochemical routes, including supercritical water gasification and pyrolysis, generate fuel-grade gases and oils from ABS blends. Mechanical recycling remains industrially viable when recycled ABS is blended with virgin resin, whereas plasma-assisted mechanochemistry has emerged as a promising technique to restore mechanical properties. These recycling technologies contribute to a circular plastic economy by improving efficiency, reducing environmental burden, and enabling the reuse of high-performance ABS materials. Full article

A series of 2-(5-phenylpyrazol-3-yl)-8-arylimino-5,6,7-trihydroquinolyliron chlorides (Fe1–Fe6) have been prepared and characterized by FT-IR spectra and elemental analysis. In single-crystal X-ray crystallography, Fe4 shows a distorted trigonal–bipyramidal geometry along with a self-assembling network through intermolecular NH···HO and OH···Cl hydrogen bonding. In the presence of MAO, all iron complexes perform with good activity and high selectivity for 1-butene. In addition, mixed solvents with different ratios of methylcyclohexane and toluene have been explored with a view to optimizing the catalytic performance. Full article

Mechanochemistry has become a fundamental method in various sciences including biology and chemistry. Despite its popularity, the mechanisms behind mechanochemically induced reactions are not very well understood. In previous work, we investigated molecular-recognition processes of molecules capable of forming racemic phases in ball mill devices. Solid-state nuclear magnetic resonance (solid-state NMR) was used as the key technique to analyze such events. We now extended this study and focused on mechanochemically induced racemic-phase formations of two representative amino acids, alanine and serine, in a resonant acoustic mixer. The data reveal the importance of adding small amounts of solvents (here water) to facilitate the underlying solid-state molecular-recognition processes. The role of water therein is further studied by deuterium magic-angle spinning (MAS) NMR experiments, also revealing that resonant acoustic mixing (RAM) enables efficient hydrogen to deuterium exchange in enantiopure serine, paving the way to deuterate organic compounds in the RAM device. Full article

MnFe₂O₄ magnetic nanoparticles have shown broad application prospects in the field of tumor diagnosis and treatment; however, precise particle size regulation within the 100–200 nm range, as well as the synergistic integration of physical and medical functionalities, remains challenging. As a commonly used method for synthesizing MnFe₂O₄ nanoparticles, the solvothermal method has been proven to enable the regulation of the particle size of products, particularly its ability to utilize the viscosity of solvents as a method for particle size regulation. Therefore, this work investigates the influence of the diethylene glycol (DEG) to ethylene glycol (EG) ratio on particle size regulation in solvothermal synthesis of MnFe₂O₄ nanoparticles, and constructs MnFe₂O₄@PB nanocomposite materials. The results demonstrate that with the DEG ratio increasing from 0 to 80% in a DEG:EG mixed solvent system, the average particle size of MnFe₂O₄ nanoparticles can be reduced from 266 nm to 105 nm. The MPB4.5 sample (MnFe₂O₄:PB molar ratio = 5:4.5 in the MnFe₂O₄@PB nanostructure) exhibits an optimal photothermal heating effect and good photothermal stability, demonstrating potential as a photothermal therapeutic agent. The resultant MnFe₂O₄@PB system provides a strategy for precise particle size regulation and functional integration for photothermal therapy of tumors with magnetic targeting potential. Full article

Recently, there has been increased interest in NASICON-type electrodes for sodium-ion batteries due to their unique combination of intercalation properties, low cost, and safety. However, their commercialization is hindered by the low electrical conductivity. One strategy to overcome this issue is to integrate NASICON materials with carbon additives. This study shows that carbon additives improve the sodium storage performance of a NASICON-type electrode in various ways, depending on the additives’ functional groups, texture, and conductivity properties. The proof-of-concept is based on a multi-electron phospho-sulphate electrode, NaFeVPO₄(SO₄)₂ (NFVPS) mixed with carbon black (C) and reduced graphene oxide (rGO). Carbon-coated samples are obtained via a simple ball milling procedure followed by thermal treatment in an argon flow. Sodium storage in the composites occurs through capacitive and Faradaic reactions. The Faradaic reaction is facilitated at the carbon black composite, while the capacitive reaction dominates for the rGO composite. NFVPS operates through two-electron reactions at 20 °C, while the increased temperatures favor the three-electron reaction. The rGO composite outperforms the carbon black composite in terms of cycling stability and rate capability at 20 and 40 °C. The role of the rGO and carbon black in electrochemical performance is discussed based on the different reactivity of hydroxyl/epoxide and carbonyl functional groups with the electrolyte salt, NaPF₆, and the solvent, polypropylene carbonate. Full article