Search Results (159)

The growing prevalence of bacterial infections and the alarming rise of antimicrobial resistance (AMR) have driven the need for innovative antimicrobial coatings for medical implants and biomaterials. However, implant surface properties, such as roughness, chemistry, and reactivity, critically influence biological interactions and must be engineered to ensure biocompatibility, corrosion resistance, and sustained antibacterial activity. This review evaluates three principal categories of antimicrobial agents utilized in surface functionalization: metal/metaloxide nanoparticles, antibiotics, and phytochemical compounds. Metal/metaloxide-based coatings, especially those incorporating silver (Ag), zinc oxide (ZnO), and copper oxide (CuO), offer broad-spectrum antimicrobial efficacy through mechanisms such as reactive oxygen species (ROS) generation and bacterial membrane disruption, with a reduced risk of resistance development. Antibiotic-based coatings enable localized drug delivery but often face limitations related to burst release, cytotoxicity, and diminishing effectiveness against multidrug-resistant (MDR) strains. In contrast, phytochemical-derived coatings—using bioactive plant compounds such as curcumin, eugenol, and quercetin—present a promising, biocompatible, and sustainable alternative. These agents not only exhibit antimicrobial properties but also provide anti-inflammatory, antioxidant, and osteogenic benefits, making them multifunctional tools for implant surface modification. The integration of these antimicrobial strategies aims to reduce bacterial adhesion, inhibit biofilm formation, and enhance tissue regeneration. By leveraging the synergistic effects of metal/metaloxide nanoparticles, antibiotics, and phytochemicals, next-generation implant coatings hold the potential to significantly improve infection control and clinical outcomes in implant-based therapies. Full article

This investigation focuses on synthesizing ZSM-5 zeolite from kaolin clay and its application as a catalytic converter to reduce NOx emissions in CRDI diesel engines. By doping the synthesized zeolite with CuCl₂ and AgNO₃ and coating it on a ceramic monolith, this study demonstrated superior catalytic activity for NO_x reduction compared to conventional converters. A set of experimental trials conducted by using a diesel engine with an AVL DI-gas analyzer showed that CuCl₂-ZSM5 and AgNO₃-ZSM5 catalysts reduced the NO_x conversion efficiencies to 72% and 66%. Additionally, these catalysts effectively reduced CO and HC emissions. The results highlight the potential of kaolin-derived zeolites with copper and cobalt dopants as efficient catalysts for emission control in internal combustion engines, offering a promising, sustainable solution for improving air quality and environmental sustainability. Full article

In the first part of this study, Y₂O₃-doped copper thiocyanate (CuSCN) with different x wt% (named CuSCN-xY, x = 0, 1, 2, and 3) films were synthesized onto ITO substrates using the spin coating method. UV-vis, SEM, AFM, EDS, and cyclic voltammetry were used to investigate the material properties of the proposed films. The conductivity and carrier mobility of the films increased with additional yttrium doping. It was found that the films with 2% Y₂O₃ (CuSCN-2Y) have the smallest valence band edges (5.28 eV). Meanwhile, CuSCN-2Y films demonstrated the densest surface morphology and the smallest surface roughness (22.8 nm), along with the highest conductivity value of 764 S cm⁻¹. Then, P-I-N self-powered UV photodetectors (PDs) were fabricated using the ITO substrate/ZnO seed layer/ZnO nanorod/CsPbBr₃/CuSCN-xY/Ag structure, and the characteristics of the devices were measured. In terms of response time, the rise time and fall time were reduced from 26 ms/22 ms to 9 ms/5 ms; the responsivity was increased from 243 mA/W to 534 mA/W, and the on/off ratio was increased to 2.47 × 10⁶. The results showed that Y₂O₃ doping also helped improve the P-I-N photodetector’s device performance, and the mechanisms were investigated. Compared with other published P-I-N self-powered photodetectors, our proposed devices show a fairly high on/off ratio, quick response times, and high responsivity and detectivity. Full article

This study comprehensively examines the barrier properties, aging behavior, and failure mechanisms of Parylene F-VT4 films, applied at four distinct thicknesses (0.3 µm, 0.6 µm, 0.9 µm, and 1.2 µm), as encapsulation layers for implantable medical devices. Parylene F-VT4, a fluorinated polymer known for its mechanical flexibility, thermal stability, and chemical inertness, is a promising candidate for long-term hermetic encapsulation. Parylene F-VT4 was uniformly deposited via a dedicated chemical vapor deposition (CVD) process typically used for Parylene depositions. The investigation of the Parylene F-VT4 films included pinhole density characterization, electrochemical impedance spectroscopy (EIS), and testing of coating lifetime based on the resistance of Cu meanders protected by Parylene F-VT4 when immersed in phosphate-buffered saline (PBS) under accelerated aging conditions (PBS at 60 °C) over 550 days. The EIS results demonstrated that thicker coatings (1.2 µm) exhibited excellent barrier properties and resistance to electrolyte penetration, whereas thinner coatings (0.3 µm and 0.6 µm) showed more rapid degradation due to microvoids and pinholes. The temporal evaluation of EIS spectra highlighted the gradual decrease in impedance magnitude, indicating the ingress of ions and water into the coating. The lifetime in PBS at 60 °C was determined by resistance-based lifetime measurements on Cu meander structures coated with Parylene F-VT4 coatings. The lifetime at 37 °C was calculated, assuming an acceleration factor of 2 per 10 °C increase in temperature, yielding lifetimes of approximately 25 days, 6.4 months, 2.3 years, and 4.5 years for 0.3 µm, 0.6 µm, 0.9 µm, and 1.2 µm coatings, respectively. These findings highlight the critical relationship between thickness and durability, providing valuable insights into the long-term performance of thin Parylene F-VT4 films for implantable devices. Full article

Bacterial infections are the primary cause of mastitis in dairy cattle. Fungal mastitis occurs in 1–12% of cases. Antibiotic therapy, the standard treatment for mastitis, has led to antibiotic-resistant bacteria, reducing treatment efficacy and increasing fungal mastitis occurrence. Antibiotics lack biocidal effects on fungi, which often exhibit resistance to antifungal agents. This study evaluated the antifungal properties of nanoparticles (NPs) against Candida albicans, Candida glabrata, Candida parapsilosis, Diutina rugosa var. rugosa, Diutina catenulata, and Diutina rugosa. Tested NPs included gold (AuNPs), silver (AgNPs), copper (CuNPs), iron with hydrophilic carbon coating (FeCNPs) (1.56–25 mg/L), and platinum (PtNPs) (0.625–10 mg/L), along with their complexes. Minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC) at 0.75–25 mg/L for AuNPs, AgNPs, CuNPs, and FeCNPs and 0.313–10 mg/L for PtNPs, as well as fungal sensitivity to standard antifungals, were determined. Each strain showed different sensitivities depending on the NPs used and their concentrations. C. glabrata was the most resistant to nanoparticles, while D. catenulata was the most susceptible. PtNPs and FeCNPs showed no or weak biocidal properties. Some mycotic-resistant strains were sensitive to nanoparticles. This study indicates a high in vitro antifungal potential for the application of nanoparticles, especially AgCuNPs, as a new effective non-antibiotic agent for the prevention and control of mycotic mastitis in dairy cattle. 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

This study attempts to use fly ash as the brazing filler additive to increase the sustainable use of coal-fired power plant by-product materials. The experimental results show that adding 5 wt% fly ash into the Ag paste filler contributes to the interfacial reactions in heterogeneous reactive air brazing (RAB) of the ZrO₂ and Crofer alloy. The Ag-rich phase dominates the brazed zone. The interfacial reaction layers contain oxidation of the Cu-Ti coating layer, Crofer alloy, and the Si/Al-rich oxides from the fly ash particles. The 5% fly ash RAB joint maintained airtightness for 280 h under 2 psig helium at room temperature. When the test temperature was raised to 600 °C for 24 h, the pressure of the joint assembly still did not drop. When the fly ash addition was increased to 10 wt%, the joint assembly was no longer leak-free at room temperature. Many visible voids and cracks exist in the brazed zone and at the ZrO₂/braze and braze/Crofer interfaces. A high volume fraction of the fly ash particles results in many brittle Si/Al-rich oxides in the joint after RAB, and the fracture of these oxides significantly deteriorates the airtightness of the joint. This study shows the feasibility and potential of introducing 5 wt% fly ash particles to the Ag-rich paste filler during the RAB of ZrO₂ and Crofer for airtight applications. Full article

Copper nanowires (Cu NWs) are considered a promising alternative to indium tin oxide (ITO) and silver nanowires (Ag NWs) due to their excellent electrical conductivity, mechanical properties, abundant reserves, and low cost. They have been widely applied in various optoelectronic devices. In this study, Cu NWs were synthesized using copper chloride (CuCl₂) as the precursor, monoethanolamine (MEA) as the complexing agent, and hydrated hydrazine (N₂H₄) as the reducing agent under strongly alkaline conditions at 60 °C. Notably, this is the first time that MEA has been employed as a complexing agent in this synthesis method for Cu NWs. Through a series of experiments, the optimal conditions for the CuCl₂–MEA–N₂H₄ system in Cu NWs synthesis were determined. This study revealed that the presence of amines plays a crucial role in nanowire formation, as the co-ordination of MEA with copper in this system provides selectivity for the nanowire growth direction. MEA prevents the excessive conversion of Cu(I) complexes into Cu₂O octahedral precipitates and exhibits an adsorption effect during Cu NWs formation. The different adsorption tendencies of MEA at the nanowire ends and lateral surfaces, depending on its concentration, influence the growth of the Cu NWs, as directly reflected by changes in their diameter and length. At an MEA concentration of 210 mM, the synthesized Cu NWs have an average diameter of approximately 101 nm and a length of about 28 μm. To fabricate transparent conductive films, the Cu NW network was transferred onto a polyethylene terephthalate (PET) substrate by applying a pressure of 20 MPa using a tablet press to ensure strong adhesion between the Cu NW-coated mixed cellulose ester (MCE) filter membrane and the PET substrate. Subsequently, the MCE membrane was dissolved by acetone and isopropanol immersion. The resulting Cu NW transparent conductive film exhibited a sheet resistance of 52 Ω sq⁻¹ with an optical transmittance of 86.7%. 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

The polyol method under a single pot has successfully produced a coating of CuO, TiO₂, and the combination of CuO/TiO₂ around Ag NWs under sequential addition. The Ag NWs and their coating with a pure metal oxide and a hybrid of metal oxide were characterized using X-ray diffraction (XRD), scanning electron microscopy (SEM) coupled with EDX, X-ray photoelectron spectroscopy (XPS), UV–Visible, photoluminescent (PL) spectroscopy, and cyclic voltammetry (CV). The formation of ultra-thin NWs was also been seen in the presence of the TiO₂ coating. The ultra-thin and co-axial coating of each metal oxide and their hybrid form preserved the SPR of the Ag NWs and demonstrated photon harvesting from the 400–800 nm range. The band gap hybridization was confirmed by CV for the Ag@CuO/TiO₂ design, which made the structure a reliable catalyst. Therefore, the material expresses excellent photocatalytic activities for carcinogenic textile dyes such as turquoise blue (TB), sapphire blue (SB), and methyl orange (MO), with and without the reagent H₂O₂. The hybrid form (i.e., Ag@CuO/TiO₂) exhibited degradation within 6 min in the presence of H₂O₂. Additionally, the material showed antibacterial activities against various bacteria (Pseudomonas aeruginosa, Escherichia coli, Staphylococcus aureus, Bacillus subtilis, and Bacillus pumilus) when assayed using broth media. Therefore, the materials have established degrading and disinfection roles suitable for environmental perspectives. The role of coating with each metal oxide and their hybrid texture further improved the growth of Ag NWs. The preparatory route possibly ensued metal–metal oxide and metal–hybrid metal oxide Schottky junctions, which would expectedly transform it into a diode material for electronic applications. Full article

This article compares the antibacterial properties of single-layer (Ag) and two-layer (Ag,Cu) coatings deposited onto a polypropylene mesh (endoprostheses for hernioplasty) in various gaseous environments (argon or nitrogen) via magnetron sputtering. The microstructure and elemental composition of the coatings were studied via SEM and TEM. The antimicrobial activity of sterile samples was investigated using the Staphylococcus aureus strain. To prevent the overheating of the polymer samples during the coating process, it is advisable to carry out pulse processing (the total coating formation time is divided into cycles of switching the magnetron on and off for equal periods). All the samples, with both single- and double-layer coatings, exhibited good antibacterial properties; however, the Cu–Ag coating enhanced the antimicrobial effect, increasing it from 97.00 to 99.97%. The glow-discharge plasma etching of the samples with a double-layer coating led to the mixing of the copper and silver layers and an increase in the surface copper content, though this did not affect the antibacterial properties of the samples. Full article

Calcium orthophosphate material (Ca_1-xCu_x)HPO₄.nH₂O (0.4 ≤ x ≤ 1) with the gradual replacement of Ca²⁺ with Cu²⁺ ions were synthesized by a chemical precipitation technique. Samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Then, the prepared powders were deposited onto an alumina substrate with interdigitated Pt electrodes by the spin coating method and polyvinyl alcohol (PVA) as a binder. Successively, the sensors were investigated from 0% to 90% at room temperature under various conditions, including humidity, nitrogenous oxide, methane, carbon dioxide and ammonia. The results evidenced that at 90% RH, the sensitivity of sensors significantly increased with the increase in the Cu content. Moreover, the sensors exhibited good repeatability and, after 1 year of aging, the sensor response was equal to 34% that of the freshly prepared sensor. Finally, there was no interference in the presence of other gases (nitrogenous oxide 2.5 ppm, methane 10 ppm, carbon dioxide 500 ppm and ammonia 4 ppm). Full article

Silver-coated copper (Ag-coated Cu) powder, combining the cost-effectiveness of copper with the oxidation resistance of silver, holds significant application value in photovoltaics and electronic pastes. In this study, Ag-coated Cu powder with a dense, uniform, smooth, and fully covered silver layer, as well as excellent dispersibility, was successfully prepared using the combined effects of ultrasonic and mechanical stirring. This study systematically analyzed the effects of different stirring conditions (mechanical stirring alone and mechanical stirring with ultrasonic oscillation), reaction rates (silver–ammonia solution supply rates of 1 mL/min to 9 mL/min), and silver contents (18%, 24%, and 28%) on the surface morphology and oxidation resistance of Ag-coated Cu powder. The results show that in the absence of ultrasonic oscillation, the uniformity and coverage of the silver layer were poor, with significant copper particle dissolution leading to hollow silver shells. Ultrasonic oscillation effectively reduced the roughness of the silver layer, improving its uniformity and coverage. Increasing the reaction rate had a minimal impact on the surface morphology but reduced the oxidation resistance of the powder. This study also analyzed the formation mechanisms of Ag-coated Cu with different surface morphologies, providing valuable guidance for producing high-quality Ag-coated Cu powder. Full article

A mechanically robust flexible transparent conductor with high thermal and chemical stability was fabricated from welded silver nanowire networks (w-Ag-NWs) sandwiched between multilayer graphene (MLG) and polyimide (PI) films. By modifying the gas flow dynamics and surface chemistry of the Cu surface during graphene growth, a highly crystalline and uniform MLG film was obtained on the Cu foil, which was then directly coated on the Ag-NW networks to serve as a barrier material. It was found that the highly crystalline layers in the MLG film compensate for structural defects, thus forming a perfect barrier film to shield Ag NWs from oxidation and sulfurization. MLG/w-Ag-NW composites were then embedded into the surface of a transparent and colorless PI thin film by spin-coating. This allowed the MLG/w-Ag-NW/PI composite to retain its original structural integrity due to the intrinsic physical and chemical properties of PI, which also served effectively as a binder. In view of its unique sandwich structure and the chemical welding of the Ag NWs, the flexible substrate-cum-electrode had an average sheet resistance of ≈34 Ω/sq and a transmittance of ≈91% in the visible range, and also showed excellent stability against high-temperature annealing and sulfurization. Full article