Search Results (30)

Fiber-shaped electrical heaters with high flexibility and excellent adaptability make an ideal candidate for the application of wearable electronics but still suffer from low strength and poor durability. Herein, an all-in-one Joule-heating fiber capable of outstanding mechanical properties, good heating efficiency, and long-term stability is reported by using polymer-assisted metal deposition to firmly coat Cu nanoparticles on high-performance liquid crystal polymer (LCP) fibers. Taking advantage of LCP, the resultant fibers exhibit a satisfying temperature threshold (up to 200 °C) and immense strength (2.94 GPa). By virtue of dense and continuous Cu film, these fibers show low electrical resistance (5.51 Ω/cm) and an ultrafast response rate (12.6 °C·s⁻¹) at low supplied voltages (0.5–3.5 V). Benefiting from the levodopa/polyethyleneimine interface design, such fibers maintain nearly constant resistance after repeatable bending, folding, and even washing (50 cycles). Based on the above-mentioned merits, a wearable patch with a Joule-heating function is knitted by using as-made fibers to offer therapeutic benefits for human body joints. This work demonstrates prospective potential for enriching the challenging applications of fiber-shaped electrical heating systems. Full article

In the context of the global energy structure transformation, concentrated solar power (CSP) technology has gained significant attention. Its future trajectory is oriented towards the construction of ultra-high temperature (700–1000 °C) power plants, aiming to enhance thermoelectric conversion efficiency and economic competitiveness. Chloride molten salts, serving as a crucial heat transfer and storage medium in the third-generation CSP system, offer numerous advantages. However, they are highly corrosive to metal materials. This paper provides a comprehensive review of the corrosion behaviors of stainless steels and high-temperature alloys in molten salts. It analyzes the impacts of factors such as temperature and oxygen, and it summarizes various corrosion types, including intergranular corrosion and hot corrosion, along with their underlying mechanisms. Simultaneously, it presents an overview of the types, characteristics, impurity effects, and purification methods of molten salts used for high-temperature heat storage and heat transfer. Moreover, it explores novel technologies such as alternative molten salts, solid particles, gases, liquid metals, and the carbon dioxide Brayton cycle, as well as research directions for improving material performance, like the application of nanoparticles and surface coatings. At present, the corrosion of metal materials in high-temperature molten salts poses a significant bottleneck in the development of CSP. Future research should prioritize the development of commercial alloy materials resistant to chloride molten salt corrosion and conduct in-depth investigations into related influencing factors. This will provide essential support for the advancement of CSP technology. Full article

This review analyzes the use of magnetite-based catalysts in various oxidation reactions. It is shown that magnetite-based catalysts are the most promising candidates from the standpoint of easy separation from the reaction zone and reusability. Diverse examples of the use of magnetite-based composites are discussed, including the following reactions: partial oxidation of methane to formaldehyde; the oxidation of cycloalkanes into alcohols and ketones; the oxidation of alkenes and alcohols with the major focus made on benzylic alcohol oxidation; oxidative cracking of alkenes; Fenton-type reactions with H₂O₂ as a benign oxidant; the removal of dyestuff in water (including wastewater by oxidation); reactions of sulfides and thiols; the oxidation of 5-hydroxymethylfurfural as a platform chemical to 2,5-diformylfuran; the oxidation of D-glucose to D-gluconic acid; and the electrocatalytic oxidation of methanol and ethanol. The most important and best-studied applications of magnetic nanoparticles in the oxidation reactions are believed to be the oxidation of diverse benzylic alcohols and D-glucose, and Fenton-like reactions aiming at the removal of S- and N-compounds from ware and fuels. Magnetic nanocomposites are determined as the materials meeting a range of criteria: (1) they should be magnetic, (2) they contain nanoparticles, and (3) they consist of two (or more) nanocomponents. The core–shell materials with magnetic nanoparticles used as a core or as decorating nanoparticles are discussed in the review. Three main types of magnetic nanocomposites can be distinguished: (1) the systems where the magnetic phase is active in the considered reaction, for instance, Fenton-like oxidation; (2) the systems containing active metal nanoparticles supported onto the magnetic nanoparticles; and (3) materials with magnetic nanoparticles as a core coated with one or two shells (porous or non-porous), with the magnetic nanoparticles being active or not in the title reaction. Magnetic nanoparticles exhibit a number of advantages compared with supported non-magnetic catalysts of oxidation reactions. The advantages include the possibility of separation from the reaction medium (5–10 times) without a significant loss of the activity, their non-toxicity, low cost, and availability, and the easy preparation of these materials. The drawbacks may include the leaching of active components; a decrease in saturation magnetization in comparison with the bulk magnetite; a limited accessibility of active sites due to diffusion through the shells; the complicated composition and structure of the nanomaterials; a decrease in the activity and specific surface area; and a limited number of magnetic compounds with acceptable characteristics. Nevertheless, the advantages of magnetic nanocatalysts stimulate their wide use in liquid-phase oxidation reactions, which will be discussed in the review. Future perspectives on the use of magnetic composites are considered. Full article

This paper presents a simple, fast, and cost-effective method for creating metallic microstructured surfaces by spray-coating a dispersion of copper nanoparticles (CuNPs) onto polymethyl methacrylate (PMMA) substrates, enabling the imbibition-induced wetting of liquid metal. The formation of these microstructured patterns is crucial for the spontaneous wetting of gallium-based liquid metals. Traditional techniques for producing such microstructures often involve complex and costly lithography and vacuum deposition methods. In contrast, this study demonstrates that liquid metal wetting can occur with metal microstructures formed through a straightforward spray-coating process. To immobilize the CuNPs on the polymer substrate, an organic solvent that dissolves the polymer surface was employed as the dispersion medium. The effects of various spray-coating parameters, including distance and time, on the uniformity and immobilization of CuNP films were systematically investigated. Under optimal conditions (120 s of spray time and 10 cm spray distance), CuNPs dispersed in dichloromethane (DCM) yielded uniform and stable microstructured surfaces. The spontaneous wetting of gallium-based liquid metal was observed on the fabricated CuNP film. Additionally, liquid metal selectively wet the CuNP patterns formed by stencil techniques, establishing electrical connections between electrodes. These findings underscore the potential of spray-coating for fabricating metallic surfaces to drive the formation of liquid metal patterns in flexible electronics applications. Full article

To enhance the anticorrosion properties of molybdenum metal in liquid zinc, this study successfully fabricated TiB₂ coatings on molybdenum substrates via the molten salt electrophoretic deposition technique and investigated their corrosion resistance in molten zinc. Initially, TiB₂ nanoparticles with a size ranging from 50 to 150 nm were synthesized using the borothermal reduction method in a molten NaF-AlF₃ bath at 1238 K. Subsequently, the electrophoretic deposition experiment was conducted under a cell voltage of 1.2 V (i.e., 0.6 V/cm) for a duration of 1 h in the melt containing TiB₂ nanoparticles, resulting in a uniform, continuous, and compact TiB₂ coating (35 μm thick) on the molybdenum substrate. Moreover, the corrosion resistance of the TiB₂-coated molybdenum metal to molten zinc was tested through continuous immersion. After 120 h of immersion, the TiB₂ coating showed no signs of cracking or peeling off, successfully protecting the molybdenum metal substrate from corrosion by molten zinc. The results confirm that the molten salt electrophoretic deposition technique can be used to prepare TiB₂ coatings with good resistance to molten zinc corrosion on molybdenum metal. Full article

This text discusses the synthesis of copper nanoparticles via a liquid phase reduction method, using ascorbic acid as a reducing agent and CuSO₄·5H₂O as the copper source. The synthesized copper nanoparticles are small in size, uniformly distributed, are mostly between 100–200 nm with clear boundaries between particles, and exhibit excellent dispersibility, making them suitable for metal conductive inks. 1. The copper nanoparticles are analyzed for good antioxidation properties, because their surface is coated with PVP and ascorbic acid. This organic layer somewhat isolates the particle surface from contact with air, preventing oxidation, and accounts for about 9% of the total weight. 2. When the prepared copper nanoparticles are spread on a polyimide substrate and sintered at 250 °C for 120 min, the resistivity can be as low as 23.5 μΩ·cm, and at 350 °C for 30 min, the resistivity is only three times that of bulk copper. 3. The prepared conductive ink, printed on a polyimide substrate using a direct writing tool, shows good flexibility before and after sintering. After sintering at 300 °C for 30 min and connecting the pattern to a circuit with a diode lamp, the diode lamp is successfully lit. 4. This method produces copper nanoparticles with small size, good dispersion, and antioxidation capabilities, and the conductive ink prepared from them demonstrates good conductivity after sintering. Full article

Bisphenol A diglycidyl ether (BADGE) is widely present in the inner coating of metal food cans, from which it can migrate into food and generate harmful derivatives during storage, such as bisphenol A (2,3-dihydroxypropyl) glycidyl ether, bisphenol A (3-chloro-2-hydroxypropyl) glycidyl ether, and bisphenol A (3-chloro-2-hydroxypropyl) (2,3-dihydroxypropyl) glycidyl ether. Here, a gold-nanoparticle-based immunochromatographic strip assay based on a broad-spectrum polyclonal antibody was developed for the simultaneous detection of BADGE and its derivatives, which could be accomplished within 15 min. The quantitative analysis of the visualization results was performed using Adobe Photoshop CC 2021, and the detection limit, defined as the concentration causing 15% inhibition, was 0.97 ng/mL. The recoveries of BADGE and its derivatives at various spiking levels in canned food samples ranged from 79.86% to 93.81%. The detection results of the proposed immunochromatographic strip assay were validated via high-performance liquid chromatography, showing a good correlation coefficient (R² = 0.9580). Full article

Recently, several methods have been used for cancer treatment. Among them, chemotherapy is generally used, but general anticancer drugs may affect normal cells and tissues, causing various side effects. To reduce the side effects and increase the efficacy of anticancer drugs, a folate-based liquid-metal drug nanodelivery system was used to target the folate receptor, which is highly expressed in cancer cells. A phospholipid-based surface coating was formed on the surface of liquid-metal nanoparticles to increase their stability, and doxorubicin was loaded as a drug delivery system. Folate on the lipid shell surface increased the efficiency of targeting cancer cells. The photothermal properties of liquid metal were confirmed by near-infrared (NIR) laser irradiation. After treating cancerous and normal cells with liquid-metal particles and NIR irradiation, the particles were specifically bound to cancer cells for drug uptake, confirming photothermal therapy as a drug delivery system that is expected to induce cancer cell death through comprehensive effects such as vascular embolization in addition to targeting cancer cells. Full article

The photocatalytic reduction of CO₂ into solar fuel is considered a promising approach to solving the energy crisis and mitigating the environmental pollution caused by anthropogenic CO₂ emission. Some powder photocatalysts have been demonstrated as efficient, but their drifting properties, along with difficult separation (catalyst and product), make continuous mode reaction very challenging, particularly in the liquid phase. In order to make this process commercially viable and economically more efficient, we have developed a simple and scalable method for immobilizing TiO₂ P25 over the surface of glass slides using an organic-based surfactant. Improved adhesion properties and the homogeneous dispersion of catalyst nanoparticles were achieved. A holder was designed with 3D printing technology in such a way that it can hold up to six slides that can be dipped simultaneously into the suspension or solution of desired materials for a uniform and homogeneous deposition. The resulting surfaces of the dip-coated materials (e.g., TiO₂ P25) were further modified by adding metallic nanoparticles and thoroughly characterized via XRD, DRS UV–Vis, SEM, and SEM–EDX. Photocatalytic tests have been performed for two major applications, viz., hydrogen production via the photoreforming of glucose and the photoreduction of CO₂ into different solar fuels. The latter tests were performed in a specially designed, high-pressure reactor with Ag/P25 supported catalysts, which exhibited about three times higher formic acid productivity (ca. 20 mol/kg_cat h) compared to the dispersed catalyst, with enhanced stability and recoverability. It is to note that catalysts deposited on the glass slides can easily be recovered and the materials did not show any weight loss. To the best of our knowledge, the obtained formic acid productivity is highest among the published literature. Full article

Separators play an essential role in lithium (Li)-based secondary batteries by preventing direct contact between the two electrodes and providing conduction pathways for Li-ions in the battery cells. However, conventional polyolefin separators exhibit insufficient electrolyte wettability and thermal stability, and in particular, they are vulnerable to Li dendritic growth, which is a significant weakness in Li-metal batteries (LMBs). To improve the safety and electrochemical performance of LMBs, Al₂O₃ nanoparticles and nanocellulose (NC)-coated non-woven poly(vinylidene fluoride)/polyacrylonitrile separators were fabricated using a simple, water-based blade coating method. The Al₂O₃/NC-coated separator possessed a reasonably porous structure and a significant number of hydroxyl groups (-OH), which enhanced electrolyte uptake (394.8%) and ionic conductivity (1.493 mS/cm). The coated separator also exhibited reduced thermal shrinkage and alleviated uncontrollable Li dendritic growth compared with a bare separator. Consequently, Li-metal battery cells with a LiNi_0.8Co_0.1Mn_0.1O₂ cathode and an Al₂O₃/NC-coated separator using either liquid or solid polymer electrolytes exhibited improved rate capability, cycle stability, and safety compared with a cell with a bare separator. The present study demonstrates that combining appropriate materials in coatings on separator surfaces can enhance the safety and electrochemical performance of LMBs. Full article

Tin oxide (SnO₂) and titanium dioxide (TiO₂) are recognized as attractive energy materials applicable for lead halide perovskite solar cells (PSCs). Sintering is one of the effective strategies for improving the carrier transport of semiconductor nanomaterials. Using the alternative metal-oxide-based ETL, nanoparticles are often used in a way that they are dispersed in a precursor liquid prior to their thin-film deposition. Currently, the creation of PSCs using nanostructured Sn/Ti oxide thin-film ETL is one of the topical issues for the development of high-efficiency PSCs. Here, we demonstrate the preparation of terpineol/PEG-based fluid containing both tin and titanium compounds that can be utilized for the formation of a hybrid Sn/Ti oxide ETL on a conductive substrate (F-doped SnO₂ glass substrate: FTO). We also pay attention to the structural analysis of the Sn/Ti metal oxide formation at the nanoscale using a high-resolution transmission electron microscope (HR-TEM). The variation of the nanofluid composition, i.e., the concentration of tin and titanium sources, was examined to obtain a uniform transparent thin film by spin-coating and sintering processes. The maximum power conversion efficiency was obtained for the concentration condition of [SnCl₂·2H₂O]/[titanium tetraisopropoxide (TTIP)] = 25:75 in the terpineol/PEG-based precursor solution. Our method for preparing the ETL nanomaterials provides useful guidance for the creation of high-performance PSCs using the sintering method. Full article

This work reports the formation of silver nanoparticles (AgNPs) by sputter deposition in thin films of three different ionic liquids (ILs) with the same anion (bis(trifluoromethylsulfonyl)imide) and cation (imidazolium), but with different alkyl chain lengths and symmetries in the cationic moiety ([C₄C₁im][NTf₂], [C₂C₂im][NTf₂], and [C₅C₅im][NTf₂]). Ionic liquid (IL) films in the form of microdroplets with different thicknesses (200 to 800 monolayers) were obtained through vacuum thermal evaporation onto glass substrates coated with indium tin oxide (ITO). The sputtering process of the Ag onto the ILs when conducted simultaneously with argon plasma promoted the coalescence of the ILs’ droplets and the formation, incorporation, and stabilization of the metallic nanoparticles in the coalesced IL films. The formation/stabilization of the AgNPs in the IL films was confirmed using high-resolution scanning electron microscopy (SEM) and UV-Vis spectroscopy. It was found that the IL films with larger thicknesses (600 and 800 monolayers) were better media for the formation of AgNPs. Among the ILs used, [C₅C₅im][NTf₂] was found to be particularly promising for the stabilization of AgNPs. The use of larger IL droplets as capture media was found to promote a better stabilization of the AgNPs, thereby reducing their tendency to aggregate. Full article

Nanoparticles widely exist in nature and may be formed through inorganic or organic pathways, exhibiting unique physical and chemical properties different from those of bulk materials. However, little is known about the potential consequences of nanomaterials on microbes in natural environments. Herein, we investigated the interactions between microbes and nanoparticles by performing experiments on the inhibition effects of gold, ludox and laponite nanoparticles on Escherichia coli in liquid Luria–Bertani (LB) medium at different nanoparticle concentrations. These nanoparticles were shown to be effective bactericides. Scanning electron microscopy (SEM) images revealed the distinct aggregation of cells and nanoparticles. Transmission electron microscopy (TEM) images showed considerable cell membrane disruption due to nanoparticle accumulation on the cell surfaces, resulting in cell death. We hypothesized that this nanoparticle accumulation on the cell surfaces not only disrupted the cell membranes but also physically blocked the microbes from accessing nutrients. An iron-reducing bacterium, Shewanella putrefaciens, was tested for its ability to reduce the Fe (III) in solid ferrihydrite (HFO) or aqueous ferric citrate in the presence of laponite nanoparticles. It was found that the laponite nanoparticles inhibited the reduction of the Fe (III) in solid ferrihydrite. Moreover, direct contact between the cells and solid Fe (III) coated with the laponite nanoparticles was physically blocked, as confirmed by SEM images and particle size measurements. However, the laponite particles had an insignificant effect on the extent of aqueous Fe (III) bioreduction but slightly enhanced the rate of bioreduction of the Fe (III) in aqueous ferric citrate. The slightly increased rate of bioreduction by laponite nanoparticles may be due to the removal of inhibitory Fe (II) from the cell surface by its sorption onto the laponite nanoparticle surface. This result indicates that the scavenging of toxic heavy metals, such as Fe (II), by nanoparticles may be beneficial for microbes in the environment. On the other hand, microbial cells are also capable of detoxifying nanoparticles by coagulating nanoparticles with extracellular polymeric substances or by changing nanoparticle morphologies. Hence, the interactions between microbes and nanoparticles in natural environments should receive more attention. Full article

This paper reports the results of the large-scale field testing of composite materials with antibacterial properties in a tropical climate. The composite materials, based on a cotton fabric with a coating of metal oxide nanoparticles (TiO₂ and/or ZnO), were produced using high-power ultrasonic treatment. The antibacterial properties of the materials were studied in laboratory tests on solid and liquid nutrient media using bacteria of different taxonomic groups (Escherichia coli, Chromobacterium violaceum, Pseudomonas chlororaphis). On solid media, the coatings were able to achieve a >50% decrease in the number of bacteria. The field tests were carried out in a tropical climate, at the Climate test station “Hoa Lac” (Hanoi city, Vietnam). The composite materials demonstrated long-term antibacterial activity in the tropical climate: the number of microorganisms remained within the range of 1–3% in comparison with the control sample for the duration of the experiment (3 months). Ten of the microorganisms that most frequently occurred on the surface of the coated textiles were identified. The bacteria were harmless, while the fungi were pathogenic and contributed to fabric deterioration. Tensile strength deterioration was also studied, with the fabrics coated with metal oxides demonstrating a better preservation of their mechanical characteristics over time, (there was a 42% tensile strength decrease for the reference non-coated sample and a 21% decrease for the sample with a ZnO + CTAB coating). Full article

Aqueous rechargeable zinc-ion batteries (ARZIBs) are potential candidates for grid-scale energy storage applications. In addition to its reversible chemistry in aqueous electrolytes, Zn metal is stable in water and air. However, there are critical challenges, such as non-uniform plating, hydrogen evolution, corrosion, and the formation of a passivation layer, which must be addressed before practical applications. In this study, the surface of Zn metal was coated with room-temperature bulk liquid-metal and liquid-metal nanoparticles to facilitate the uniform plating of Zn–ions during cycling. A simple probe ultrasonication method was used to prepare the liquid-metal nanoparticles, and a nanoparticle suspension film was formed through spin coating. At an areal capacity and current density of 0.5 mAh cm⁻² and 0.5 mA cm⁻², respectively, symmetric cells composed of bare Zn metal electrodes were prone to short-circuiting after ~45 h of deposition/striping cycles. However, under the same operating conditions, symmetric cells employing the room-temperature liquid-metal-coated electrodes operated stably for more than 500 h. Compared to the symmetric cell with bare Zn, the symmetric cell with the bulk liquid-metal coated electrode exhibited a significant reduction in the initial nucleation barrier, with respective values of 113.2 and 10.1 mV. Electrochemical characterization of practical full cells also showed significant improvements in the capacity and cycling performance derived from the room-temperature liquid-metal coating. Full article