Search Results (315)

In this study, a simple and effective approach was developed for the quantitative detection of serotonin. Hexagonal copper selenide nanostructures (CuSe) were employed to modify a disposable screen-printed carbon electrode (SPCE), and their ability to electrochemically detect serotonin in serum samples was investigated. The fabricated CuSe nanostructures exhibited an interconnected, cluster-like morphology composed of irregularly shaped particles with a distinct hexagonal crystal structure. The electrochemical results revealed that the CuSe/SPCE sensor showed better electrochemical activity and good analytical sensing performance towards serotonin detection. The sensor exhibited a linear response in the concentration range of 10 to 1000 nM, with an excellent correlation coefficient (R² = 0.9998) and a low detection limit of 3 nM. Furthermore, the CuSe/SPCE showed better selectivity, impressive sensitivity (12.45 µM/µA cm⁻²), and good reproducibility toward serotonin detection, making it a promising electrochemical biosensor for serotonin detection in various real biological samples. Full article

The article suggests a simple one-step sol–gel method for synthesizing nanostructured zinc oxide films co-doped with copper and aluminum. It shows the possibility of forming hierarchical ZnO:Al:Cu nanostructures combining branches of different sizes and ranks and quasi-spherical fractal aggregates. It demonstrates the use of the synthesized samples as highly efficient photocatalysts providing the decomposition of toxic dyes (methyl orange) under the action of both ultraviolet radiation and visible light. It establishes the contribution of the average crystallite size, the proportion of zinc atoms in the crystalline phase, their nanostructure, as well as X-ray amorphous phases of copper and aluminum to the efficiency of the photocatalysis process. Full article

Polymer brushes (PBs) are transformative surface-modifying nanostructures, yet their synthesis via controlled methods like copper-mediated surface-initiated atom-transfer radical polymerization (Cu⁰-SI-ATRP) faces reproducibility challenges due to a lack of understanding of parameter interdependencies. This study systematically evaluates the Cu⁰-SI-ATRP process for polyacrylamide brushes (PAM-PBs), aiming to clarify key parameters that influence the synthesis process. This evaluation followed a step-by-step characterization that tracked molecular changes through infrared spectroscopy (IR) and surface development by contact angle (CA) through two different mixing methods: ultrasonic mixing and process simplification (Method A) and following literature-based parameters (Method B). Both methods, consisting of surface activation, 3-aminopropyltriethoxysilane (APTES) deposition, bromoisobutyryl bromide (BiBB) anchoring, and polymerization, were analyzed by varying parameters like concentration, temperature, and time. Results showed ultrasonication during surface activation enhanced siloxane (1139→1115 cm⁻¹) and amine (1531 cm⁻¹) group availability while reducing APTES concentration to 1 Vol% without drying sufficed for BiBB anchoring. BiBB exhibited insensitivity to concentration but benefited from premixing, evidenced by sharp C–Br (~1170 cm⁻¹) and methyl (3000–2800 cm⁻¹) bands. Additionally, it was observed that PAM-PBs improved with Method A, which had reduced variance in polymer fingerprint regions compared to Method B. Adding to the above, CA measurements gave complementary step-by-step information along the modifications of the surface, revealing distinct wettability behaviors between bulk PAM and synthesized PAM-PBs (from 51° to 37°). As such, this work identifies key parameter influence (e.g., mixing, BiBB concentration), simplifies steps (drying omission, lower APTES concentration), and demonstrates a step-by-step, systematic parameter decoupling that reduces variability. In essence, this detailed parameter analysis addresses the PAM-PBs synthesis process with better reproducibility than the previously reported synthesis method and achieves the identification of characteristic behaviors across the step-by-step process without the imperative need for higher-cost characterizations. Full article

Printed electronics employ established printing methods to create low-cost, mechanically flexible devices including batteries, supercapacitors, sensors, antennas and RFID tags on plastic, paper and textile substrates. This review focuses on the specific contribution of screen printing to that landscape, examining how ink viscosity, mesh selection and squeegee dynamics govern film uniformity, pattern resolution and ultimately device performance. Recent progress in advanced ink systems is surveyed, highlighting carbon allotropes (graphene, carbon nano-onions, carbon nanotubes, graphite), silver and copper nanostructures, MXene and functional oxides that collectively enhance mechanical robustness, electrical conductivity and radio-frequency behavior. Parallel improvements in substrate engineering such as polyimide, PET, TPU, cellulose and elastomers demonstrate the technique’s capacity to accommodate complex geometries for wearable, medical and industrial applications while supporting environmentally responsible material choices such as water-borne binders and bio-based solvents. By mapping two decades of developments across energy-storage layers and functional electronics, the article identifies the key process elements, recurring challenges and emerging sustainable practices that will guide future optimization of screen-printing materials and protocols for high-performance, customizable and eco-friendly flexible devices. Full article

Copper-thiolate nanostructures, formed through the self-assembly of cysteine (Cys) and glutathione (GSH) with copper ions, offer a versatile platform for redox-active applications due to their structural stability and chemical functionality. In this study, Cu-Cys-GSH nanoparticles were synthesized and employed to develop a capacitive biosensor for the ultralow concentration detection of hydrogen peroxide (H₂O₂). The detection mechanism leverages a Fenton-like reaction, where H₂O₂ interacts with Cu-Cys-GSH nanoparticles to generate hydroxyl radicals (·OH) through redox cycling between Cu²⁺ and Cu⁺ ions. These redox processes induce changes in the sensor’s surface charge and dielectric properties, enabling highly sensitive capacitive sensing at gold interdigitated electrodes (IDEs). The influence of chirality on sensing performance was investigated by synthesizing nanoparticles with both L- and D-cysteine enantiomers. Comparative analysis revealed that the stereochemistry of cysteine impacts the catalytic activity and sensor response, with Cu-L-Cys-GSH nanoparticles exhibiting superior performance. Specifically, the biosensor achieved a linear detection range from 1.0 fM to 1.0 pM and demonstrated an ultra-sensitive detection limit of 21.8 aM, outperforming many existing methods for H₂O₂ detection. The sensor’s practical performance was further validated using milk and saliva samples, yielding high recovery rates and confirming its robustness and accuracy for real-world applications. This study offers a disposable, low-cost sensing platform compatible with sustainable healthcare practices and facilitates easy integration into point-of-care diagnostic systems. Full article

Solar desalination is widely regarded as an effective way to solve freshwater scarcity. However, the balance between the costs of micro-nanostructures, thermal regulation, and the durability of interface evaporators must all be considered. In this study, a super-hydrophobic copper foam with hierarchical micro-nanostructures exhibited temperatures greater than 66 °C under solar illumination of 1 kW·m⁻². Significantly, the modified copper foam acting as a solar interface evaporator had a water harvesting efficiency of 1.76 kg·m⁻²·h⁻¹, resulting from its good photothermal conversion and porous skeleton. Further, the anti-deicing, self-cleaning, and anti-abrasion tests were carried out to demonstrate its durability. The whole fabrication of the as-prepared CF was only involved in mechanical extrusion and spray-coating, which is suitable for large-scale production. This work endows the interface evaporator with super-hydrophobicity, photo-thermal conversion, anti-icing, and mechanical stability, all of which are highly demanded in multi-scenario solar desalination. Full article

Understanding the formation, structural evolution, and response of water ice at the nanoscale is essential for advancing research in fields such as cryo-electron microscopy and atmospheric science. In this work, we used environmental transmission electron microscopy (ETEM) to investigate the formation of water ice nanostructures and the etching and charging behaviors of ice under fast electron irradiation. These nanostructures were observed to be suspended along the edges of copper grids and supported on few-layer graphene. We varied growth parameters (temperature and time) to produce water ice nanostructures characterized by uniform thickness and enhanced crystallinity. Moreover, we examined the lithographic patterning of water ice at the copper grid edges and its localized etching effects on graphene substrates. Off-axis electron holography experiments further revealed charging phenomena induced by electron beam irradiation, enabling a quantitative assessment of charge accumulation on the ice nanostructures. Our findings demonstrate the controlled growth of ice thin films under high vacuum conditions at cryogenic temperatures, elucidate the etching behavior and charging phenomena of water ice under rapid electron beam irradiation. Full article

Nanotechnology is emerging as an innovative and sustainable agricultural approach that minimizes environmental impacts by developing nanostructured materials to promote plant growth and combat plant-parasitic nematodes (PPNs). Plant-based nanoparticles (NPs) are attracting increasing attention as they are more environmentally friendly, economical and biocompatible compared to traditional chemical and physical synthesis methods. The ability of plants to reduce and stabilize metal ions and form NPs of specific size and morphology through their biochemical content offers great advantages for agricultural applications. Phytochemicals produced by plants enable the biological synthesis of metal and metal oxide NPs by acting as reducing agents and coating agents in NP synthesis. The effects of plant-based NPs in nematode control are based on mechanisms such as the disruption of the nematode cuticle, induction of oxidative stress and interference with parasite metabolism. Several plant species have been investigated for the synthesis of metal and metal oxide nanoparticles such as silver (Ag-NPs), nickel oxide (NiO-NPs), zinc oxide (ZnO-NPs), copper oxide (CuO-NPs) and iron (Fe-NPs). These biologically synthesized NPs show potent biological activity against important PPNs such as Meloidogyne spp., Pratylenchus spp. and Heterodera spp. The integration of plant-derived NPs into agricultural systems has significant potential for plant growth promotion, nematode suppression and soil health improvement. This review highlights their role in reducing environmental impact in agricultural applications by examining the sustainable synthesis processes of plant-based NPs. Full article

Copper (Cu) nanoparticles, known for their high electrical conductivity and cost-effectiveness, have emerged as essential materials in various applications from flexible electronics to antimicrobial agents. This work focuses on the synthesis and characterization of semiconductive nanostructured films composed of polyvinyl alcohol (PVA) with embedded Cu nanoparticles. The study provides a comprehensive analysis of the structural, optical, electrical, and dielectric properties of the resulting nanocomposites. The results indicate a significant reduction in optical band gap, from 4.82 eV in pure PVA to 2.6–2.8 eV in the nanocomposites, alongside enhanced electrical conductivities reaching 1.20 S/cm for films with 5 wt.% Cu. Dielectric assessments further reveal high dielectric constants, underscoring the potential of these materials for flexible electronic applications. This work highlights the effectiveness of incorporating Cu nanoparticles into polymer matrices, paving the way for advanced materials that meet the demands of next-generation electronics. Full article

This study presents the preparation of hybrid iron oxide nanocomposites through a two-step process combining microfluidic-assisted synthesis and post-synthetic surface modification. Fe₃O₄ nanoparticles were synthesized and simultaneously functionalized with salicylic acid using a three-dimensional vortex-type microfluidic chip, enabling rapid and uniform particle formation. The resulting Fe₃O₄/SA nanostructures were further modified with either silver or copper oxide to form iron oxide nanocomposites with enhanced antimicrobial functionality. These nanocomposites were subsequently integrated into silica aerogel matrices using a dip-coating approach to improve surface dispersion, structural stability, and biocompatibility. The structural and morphological properties of the samples were investigated using XRD, FT-IR, TEM with SAED analysis, and Raman microscopy. In vitro cytotoxicity and antimicrobial assays demonstrated that Fe₃O₄/SA–Ag and Fe₃O₄/SA–CuO exhibit potent antibacterial activity and cell type-dependent biocompatibility. In vivo biodistribution studies showed no accumulation in major organs and selective clearance via the spleen, validating the systemic safety of the platform. These findings highlight the potential of the synthesized nanocomposites as biocompatible, antimicrobial coatings for advanced biomedical surfaces. Full article

Brasses are well-known structural materials, and their electrochemistry seems to be known. However, the formation of nanostructured anodic oxides on brasses is still not common and researched enough. Despite the electrochemical oxidation or anodization of copper and zinc being well-recognized and known in the scientific community, there is a lack of a satisfactory amount of research on brass anodizing. Both copper and zinc can passivate in neutral and alkaline electrolytes, and also the mechanism of the nanostructured oxide growth of both seems to be similar. In this review, much effort was put in to gather the information on the protocols on the electrochemical oxidations of brasses and their applications. Usually, the effects of electrochemical oxidation allow us to obtain nanostructured surfaces made of mixed Cu and Zn species. The formation of such composite nanostructures allows us to apply them in such emerging applications as photocatalytic organic pollutant decomposition, photoelectrochemical hydrogen generation, electrochemical carbon dioxide reduction reactions, or electrochemical methanol oxidation. Full article

In this study, nanostructured copper oxide-based films with crystallite size below 10 nm were electrochemically synthesized on copper foil and foam electrodes and investigated for their supercapacitive behaviour. The synthesis was carried out via cyclic voltammetry (CV) for up to 1000 cycles in an alkaline electrolyte. By tuning the upper vertex potential (−0.3 V to 0.65 V vs. Ag/AgCl), both phase composition (Cu₂O, Cu(OH)₂, CuO) and morphology (grains, nanoneedles, nanoplatelets) were precisely controlled, demonstrating the versatility of this approach. The kinetics of oxide/hydroxide film formation on foil and foam electrodes were analysed based on EIS data that were interpreted in the frame of equivalent electric circuits and their changes with potential. The capacitive properties of the synthesized films were evaluated using CV in the potential range of 0 V–0.65 V, and the optimized CuO film synthesized on Cu foam exhibited a high specific capacitance of 1380 mF cm⁻². An energy density of 0.061 mWh cm⁻² and power density of 1.28 mW cm⁻² were obtained at 10 mA cm⁻² discharge current. Charge–discharge cycling at 100 mV s⁻¹ for 1000 cycles indicated an initial capacitance increase followed by stable retention, highlighting the structural integrity and electrochemical stability of the films obtained on 3D foam. These findings provide valuable insights into the controlled electrochemical synthesis of copper oxide nanostructures and their potential for high-performance capacitor applications. Full article

This study explored the controlled formation of chiral copper(II) oxide (CuO) crystals using chiral amino acids as chirality-inducing agents. Utilizing chemical bath deposition (CBD) as the fabrication method, we achieved simple, reproducible synthesis suitable for industrial-scale applications. Our characterization of the induced chirality through high-performance liquid chromatography (HPLC), circular dichroism (CD), and isothermal titration calorimetry (ITC) revealed distinctive chiral features. These findings not only advance our understanding of chirality control in inorganic nanostructures but also establish CBD as a viable technique for the large-scale production of chiral materials. Full article

This study investigates the fabrication of nanostructured chromium thin films via selective dissolution of PVD-deposited Cu–Cr thin films. The effects of the deposition parameters on the structural, chemical, and morphological properties of the films are systematically analyzed. Starting from a thin film composed of 50 wt.% chromium and 50 wt.% copper, deposited onto a substrate pre-heated to 300 °C, we demonstrate that the following dealloying process carried out in a diluted nitric acid solution yields nanostructured chromium films with high porosity, large surface area, enhanced wettability and neglectable copper content. These findings underline the critical influence of the deposition temperature and alloy composition on achieving optimal film properties. Full article

Chemiresistive ammonia gas sensors with a low limit of detection of 0.15 ppm and moisture-independent characteristics based on p-type copper iodide (CuI) semiconductor films have been developed. CuI films were deposited on glass and polyethylene terephthalate (PET) substrates using a Successive Ionic Layer Adsorption and Reaction method to fabricate CuI/glass and CuI/PET gas sensors, respectively. They have a nanoscale morphology, an excess iodine and sulfur impurity content, a zinc blende γ-CuI crystal structure with a grain size of ~34 nm and an optical band gap of about 2.95 eV. The high selective sensitivity of both sensors to NH₃ is explained by the formation of the [Cu(NH₃)₂]⁺ complex. At 5 °C, the responses to 3 ppm ammonia in air in terms of the relative resistance change were 24.5 for the CuI/glass gas sensor and 28 for the CuI/PET gas sensor, with short response times of 50 s to 210 s and recovery times of 10–70 s. The sensors have a fast response–recovery and their performance was well maintained after long-term stability testing for 45 days. After 1000 repeated bends of the flexible CuI/PET gas sensor in different directions, with bending angles up to 180° and curvature radii up to 0.25 cm, the response changes were only 3%. Full article