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Plaque control is especially important during orthodontic treatment because areas of the teeth near brackets and wires are difficult to clean with a toothbrush, resulting in debris buildup of food or dental plaque, thus causing caries and periodontal disease. The objective of this study was to evaluate the antimicrobial properties of silver nanoparticles (AgNPs), titanium dioxide nanoparticles (TiO2NPs), and silver/titanium dioxide nanoparticles (Ag/TiO2NPs), synthesized on the surface of α-alumina ceramic brackets. The AgNPs and TiO2NPs were synthesized by a simple chemical method, and these were characterized by XRD, SEM, and XPS TEM; the antimicrobial activity was tested against Staphylococcus aureus and Escherichia coli by diffusion test. The results of this study demonstrated that by this simple chemical method, silver and titanium dioxide nanoparticles can be synthesized on the surface of α-alumina esthetic brackets, and these NPs possess good antimicrobial activity and the possibility of reducing dental caries, periodontal disease, and white spot generated during orthodontic treatment. [ABSTRACT FROM AUTHOR]

Cu6Sn5-xAg alloys (x = 0, 3, 6; %, mass fraction) were synthesized using Ag as a dopant through a high-temperature melting technique. The microstructure of the alloy was analyzed using X-ray diffraction (XRD), scanning electron microscopy (SEM), and other equipment, while the hardness of the alloy was measured to investigate the impact of Ag addition on the structure and microstructure of the Cu6Sn5 intermetallic compound. This study explored the influence of varying Ag contents on the properties of Cu6Sn5 intermetallic compounds, with calculations based on first principles revealing the mechanical properties and density of states of η′-Cu6Sn5 and its Ag-doped systems. The results indicated that Cu6Sn5-xAg alloys predominantly existed in three distinct forms, all exhibiting large masses without any impurities or precipitates. First-principle calculations demonstrated that Ag substitution in certain sites suppressed the anisotropy of the Young's modulus of Cu6Sn5, particularly in the Cu1, Cu3, Sn1, and Sn3 positions, while the effect was less significant at the Cu2, Cu4, and Sn2 sites. The introduction of Ag through doping enhanced the covalent bonding within the η′-Cu6Sn5 structure, promoting the formation of a stable (Cu, Ag)6Sn5 structure. [ABSTRACT FROM AUTHOR]

Photocatalysts with different molar ratios of Ag-modified ZnO to g-C3N4 were prepared through an electrostatic self-assembly method and characterized through techniques such as X-ray diffraction, Fourier transform infrared spectroscopy, and scanning electron microscopy. The resulting Ag-ZnO/g-C3N4 photocatalysts exhibited a unique 1D-0D-2D morphology and Z-type heterojunction. Moreover, g-C3N4 nanosheets with large layer spacing were prepared using acid treatment and thermal stripping methods. The Z-type heterostructure and localized surface plasmon resonance effect of Ag nanowires enabled high-speed electron transfer between the materials, while retaining large amounts of active substances, and broadened the light response range. Because of these features, the response current of the materials improved, and their impedance and photoluminescence reduced. Among the synthesized photocatalysts, 0.05Ag-ZnO/g-C3N4 (molar ratio of g-C3N4/ZnO: 0.05) exhibited the highest photocatalytic performance under UV–visible light. It degraded 98% of methylene blue in just 30 min, outperforming both g-C3N4 (21% degradation in 30 min) and Ag-ZnO (84% degradation in 30 min). In addition, 0.05Ag-ZnO/g-C3N4 demonstrated high cycling stability. [ABSTRACT FROM AUTHOR]

The application of Neurospora sp., a fungus that commonly thrives on complex agricultural and plant wastes, has proven successful in utilizing citrus peel waste as a source of naringin. A UV-Vis spectrophotometric method proved the biotransformation of naringin, with an absorption maximum (λmax) observed at 310 nm for the biotransformed product, naringenin (NAR). Further verification of the conversion of naringin was provided through thin layer chromatography (TLC). The Neurospora crassa mediated biotransformation of naringin to NAR was utilized for the rapid (within 5 min) synthesis of silver (Ag) and gold (Au) nanoconjugates using sunlight to accelerate the reaction. The synthesized NAR-nano Ag and NAR-nano Au conjugates exhibited monodispersed spherical and spherical as well as polygonal shaped particles, respectively. Both of the nanoconjugates showed average particle sizes of less than 90 nm from TEM analysis. The NAR-Ag and NAR-Au nanoconjugates displayed potential enhancement of the antimicrobial activities, including antibacterial and nematicidal properties over either standalone NAR or Ag or Au NPs. This study reveals the potential of naringinase-producing Neurospora sp. for transforming naringin into NAR. Additionally, the resulting NAR-Ag and NAR-Au nanoconjugates showed promise as sustainable antibiotics and biochemical nematicides. [ABSTRACT FROM AUTHOR]

The field of optical thin films has garnered significant attention due to their potential applications in visible light communication, optical sensing, and imaging. Among the various fabrication methods available, conventional layer-by-layer (LBL) dip coating is less sophisticated and more economical. Nevertheless, this approach frequently encounters deficiencies in the precise control of the growth of thin films. This work aimed at properly comprehending the growth conditions associated with the LBL dip coating process and optimizing the conditions to obtain the best thin film growth for different materials: metallic (Ag), semiconducting (ZnO), and insulating (SiO2). The optimization of the conditions for surface functionalization with 3-aminopropyltriethoxysilane (APTES) together with other parameters like dipping time, drying time, the number of dipping–drying cycles, and the timing of the intermediate APTES layers led to the controlled growth of thin films. Atomic force microscopy and scanning electron microscopy revealed even deposition in the case of ZnO and SiO2 from the very beginning, while with Ag NPs, the growth of the thin film was observed to be uneven and gradually became smooth as the number of layers increased, and a smooth layer could be observed after over 100 layers of dipping. [ABSTRACT FROM AUTHOR]

Novel Ag/Fe2O3/BiOI Z-scheme heterostructures are first fabricated through a facile hydrothermal method. The composition and properties of as-synthesized Ag/Fe2O3/BiOI nanocomposites are characterized by powder X-ray diffraction, scanning electron microscopy, high-resolution transmission electron microscopy, UV-Vis diffuse reflectance spectra, etc. The Ag/Fe2O3/BiOI systems exhibit remarkable degradation performance for tetracycline (TC). In particular, the composite (Ag/Fe2O3/BiOI-2) shows the highest efficiency when the contents of Ag and α-Fe2O3 are 2 wt% and 15%, respectively. The effects of operating parameters, including the solution pH, H2O2 concentration, TC concentration, and catalyst concentration, on the degradation efficiency are investigated. The photo-Fenton mechanism is studied, and the results indicated that •O2− is the main active specie for TC degradation. The enhanced performance of Ag/Fe2O3/BiOI heterostructures may be ascribed to the synergic effect between photocatalysis and the Fenton reaction. The formation of Ag/Fe2O3/BiOI heterojunction is beneficial to the transfer and separation of charge carriers. The photo-generated electrons accelerate the Fe2+/Fe3+ cycle and create the reductive reaction of H2O2. This research reveals that the Ag/Fe2O3/BiOI composite possesses great potential in wastewater treatment. [ABSTRACT FROM AUTHOR]

Dopamine was used to modify polytetrafluoroethylene (PTFE) in order to obtain functional polydopamine (PDA) surface-modified PTFE microporous film (PTFE@PDA). Ag was deposited on the surface of PTFE@PDA using electroless plating in order to obtain Ag-wrapped PTFE@PDA film (PTFE@Ag). A liquid-phase chemical reduction method was employed to prepare nickel nanochains. A Ni@PVDF cast film was obtained by mechanically blended nickel nanochains and polyimide (PVDF). The above two films were hot pressed to give a flexible, ultra-thin, and highly effective electromagnetic shielding composite film with a "3+2" layered structure. IR, XRD, and TEM results showed the PTFE@PDA film surface was coated by a tight plating layer of Ag particles with a particle size of 100~200 nm. PTFE@Ag+Ni@PVDF composite film exhibited excellent electromagnetic shielding effectiveness, with the conductivity of 7507.5 S/cm and the shielding effectiveness of 69.03 dB in the X-band range. After a 2000-cycle bending, this value still remained at 51.90 dB. Furthermore, the composite film presented excellent tensile strength of 62.1 MPa. It has great potential for applications in flexible and wearable intelligent devices. [ABSTRACT FROM AUTHOR]

Since printed capacitive sensors provide better sensing performance, they can be used in automotive bezel applications. It is necessary to fabricate such sensors and apply an optimization approach for choosing the optimal sensor pattern. In the present work, an effort was made to formulate interdigitated pattern-printed Silver (Ag) electrode flexible sensors and adopt the Taguchi Grey Relational (TGR)-based optimization approach to enhance the flexible sensor's panel for enhanced automobile infotainment applications. The optimization technique was performed to derive better design considerations and analyze the influence of the sensor's parameters on change in capacitance when touched and production cost. The fabricated flexible printed sensors can provide better sensing properties. A design pattern which integrates an overlap of 15 mm, an electrode line width of 0.8 mm, and an electrode gap 0.8 mm can produce a higher change in capacitance and achieve a lower weight. The overlap has a greater influence on sensor performance owing to its optimization of spatial interpolation. [ABSTRACT FROM AUTHOR]

Green nanotechnology has made the synthesis of nanoparticles a possible approach. Nanotechnology has a significant impact on several scientific domains and has diverse applications in different commercial areas. The current study aimed to develop a novel and green approach for the biosynthesis of silver oxide nanoparticles (Ag2ONPs) utilizing Parieteria alsinaefolia leaves extract as a reducing, stabilizing and capping agent. The change in color of the reaction mixture from light brown to reddish black determines the synthesis of Ag2ONPs. Further, different techniques were used to confirm the synthesis of Ag2ONPs, including UV-Visible spectroscopy, Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscope (SEM), Energy-dispersive X-ray spectroscopy (EDX), zeta potential and dynamic light scattering (DLS) analyses. The Scherrer equation determined a mean crystallite size of ~22.23 nm for Ag2ONPs. Additionally, different in vitro biological activities have been investigated and determined significant therapeutic potentials. Radical scavenging DPPH assay (79.4%), reducing power assay (62.68 ± 1.77%) and total antioxidant capacity (87.5 ± 4.8%) were evaluated to assess the antioxidative potential of Ag2ONPs. The disc diffusion method was adopted to evaluate the antibacterial and antifungal potentials of Ag2ONPs using different concentrations (125–1000 μg/mL). Moreover, the brine shrimp cytotoxicity assay was investigated and the LC50 value was calculated as 2.21 μg/mL. The biocompatibility assay using red blood cells (<200 μg/mL) confirmed the biosafe and biocompatible nature of Ag2ONPs. Alpha-amylase inhibition assay was performed and reported 66% inhibition. In conclusion, currently synthesized Ag2ONPs have exhibited strong biological potential and proved as an attractive eco-friendly candidate. In the future, this preliminary research work will be a helpful source and will open new avenues in diverse fields, including the pharmaceutical, biomedical and pharmacological sectors. [ABSTRACT FROM AUTHOR]

This study aims to examine the impact of the direct and indirect mixing techniques on the dispersion and homogeneity of magnesium oxide (MgO) and silver (Ag) nanoparticles (NPs) mixed with polymethylmethacrylate (PMMA). NPs were mixed with PMMA powder directly (non-ethanol-assisted) and indirectly (ethanol-assisted) with the aid of ethanol as solvent. X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDX), and scanning electron microscope (SEM) were used to evaluate the dispersion and homogeneity of MgO and Ag NPs within the PMMA-NPs nanocomposite matrix. Prepared discs of PMMA-MgO and PMMA-Ag nanocomposite were analyzed for dispersion and agglomeration by Stereo microscope. XRD showed that the average crystallite size of NPs within PMMA-NP nanocomposite powder was smaller in the case of ethanol-assisted mixing compared to non-ethanol-assisted mixing. Furthermore, EDX and SEM revealed good dispersion and homogeneity of both NPs on PMMA particles with ethanol-assisted mixing compared to the non-ethanol-assisted one. Again, the PMMA-MgO and PMMA-Ag nanocomposite discs were found to have better dispersion and no agglomeration with ethanol-assisted mixing when compared to the non-ethanol-assisted mixing technique. Ethanol-assisted mixing of MgO and Ag NPs with PMMA powder obtained better dispersion, better homogeneity, and no agglomeration of NPs within the PMMA-NP matrix. [ABSTRACT FROM AUTHOR]

One of the crucial challenges of our time is to effectively use metal and metal oxide nanoparticles (NPs) as an alternative way to combat drug-resistant infections. Metal and metal oxide NPs such as Ag, Ag2O, Cu, Cu2O, CuO, and ZnO have found their way against antimicrobial resistance. However, they also suffer from several limitations ranging from toxicity issues to resistance mechanisms by complex structures of bacterial communities, so-called biofilms. In this regard, scientists are urgently looking for convenient approaches to develop heterostructure synergistic nanocomposites which could overcome toxicity issues, enhance antimicrobial activity, improve thermal and mechanical stability, and increase shelf life. These nanocomposites provide a controlled release of bioactive substances into the surrounding medium, are cost effective, reproducible, and scalable for real life applications such as food additives, nanoantimicrobial coating in food technology, food preservation, optical limiters, the bio medical field, and wastewater treatment application. Naturally abundant and non-toxic Montmorillonite (MMT) is a novel support to accommodate NPs, due to its negative surface charge and control release of NPs and ions. At the time of this review, around 250 articles have been published focusing on the incorporation of Ag-, Cu-, and ZnO-based NPs into MMT support and thus furthering their introduction into polymer matrix composites dominantly used for antimicrobial application. Therefore, it is highly relevant to report a comprehensive review of Ag-, Cu-, and ZnO-modified MMT. This review provides a comprehensive overview of MMT-based nanoantimicrobials, particularly dealing with preparation methods, materials characterization, and mechanisms of action, antimicrobial activity on different bacterial strains, real life applications, and environmental and toxicity issues. [ABSTRACT FROM AUTHOR]

An enhancement of the local electric field at the metal/dielectric interface of hybrid materials due to the localized surface plasmon resonance (LSPR) phenomenon plays a particularly important role in versatile research fields resulting in a distinct modification of the electrical, as well as optical, properties of the hybrid material. In this paper, we succeeded in visually confirming the LSPR phenomenon in the crystalline tris(8-hydroxyquinoline) aluminum (Alq3) micro-rod (MR) hybridized with silver (Ag) nanowire (NW) in the form of photoluminescence (PL) characteristics. Crystalline Alq3 MRs were prepared by a self-assembly method under the mixed solution of protic and aprotic polar solvents, which could be easily applied to fabricate hybrid Alq3/Ag structures. The hybridization between the crystalline Alq3 MRs and Ag NWs was confirmed by the component analysis of the selected area electronic diffraction attached to high-resolution transmission electron microscope. Nanoscale and solid state PL experiments on the hybrid Alq3/Ag structures using a lab-made laser confocal microscope exhibited a distinct enhancement of the PL intensity (approximately 26-fold), which also supported the LSPR effects between crystalline Alq3 MRs and Ag NWs. [ABSTRACT FROM AUTHOR]

The wetting behavior of ionic liquids (ILs) on the mesoscopic scale considerably impacts a wide range of scientific fields and technologies. Particularly under vacuum conditions, these materials exhibit unique characteristics. This work explores the effect of the deposition rate and substrate temperature on the nucleation, droplet formation, and droplet spreading of ILs films obtained by thermal evaporation. Four ILs were studied, encompassing an alkylimidazolium cation (CnC1im) and either bis(trifluoromethylsulfonyl)imide (NTf2) or the triflate (OTf) as the anion. Each IL sample was simultaneously deposited on surfaces of indium tin oxide (ITO) and silver (Ag). The mass flow rate was reproducibly controlled using a Knudsen cell as an evaporation source, and the film morphology (micro- and nanodroplets) was evaluated by scanning electron microscopy (SEM). The wettability of the substrates by the ILs was notably affected by changes in mass flow rate and substrate temperature. Specifically, the results indicated that an increase in the deposition rate and/or substrate temperature intensified the droplet coalescence of [C2C1im][NTf2] and [C2C1im][OTf] on ITO surfaces. Conversely, a smaller impact was observed on the Ag surface due to the strong adhesion between the ILs and the metallic film. Furthermore, modifying the deposition parameters resulted in a noticeable differentiation in the droplet morphology obtained for [C8C1im][NTf2] and [C8C1im][OTf]. Nevertheless, droplets from long-chain ILs deposited on ITO surfaces showed intensified coalescence, regardless of the deposition rate or substrate temperature. [ABSTRACT FROM AUTHOR]

In this work, CeO2 nanoparticles, as well as CeO2 nanocomposites with plasmonic silver nanoparticles, were synthesized using a simple sol-gel process. The concentration of silver in the composites varied from 0.031–0.25 wt%. Cerium hydroxide dried gel was calcined at temperatures from 125 to 800 °C to obtain CeO2. It was shown that, at an annealing temperature of 650 °C, single-phase CeO2 nanopowders with an average particle size in the range of 10–20 nm can be obtained. The study of acid-base properties showed that with an increase in the calcination temperature from 500 to 650 °C, the concentration of active centers with pKa 9.4 and 6.4 sharply increases. An analysis of the acid-base properties of CeO2-Ag nanocomposites showed that with an increase in the silver concentration, the concentration of centers with pKa 4.1 decreases, and the number of active centers with pKa 7.4 increases. In a model experiment on dye photodegradation, it was shown that the resulting CeO2 and CeO2-Ag nanopowders have photocatalytic activity. CeO2-Ag nanocomposites, regardless of the silver concentration, demonstrated better photocatalytic activity than pure nanosized CeO2. [ABSTRACT FROM AUTHOR]

Silver–NHC (NHC = N-heterocyclic carbene) complexes play a special role in the field of transition-metal complexes due to (1) their prominent biological activity, and (2) their critical role as transfer reagents for the synthesis of metal-NHC complexes by transmetalation. However, the application of silver–NHCs in catalysis is underdeveloped, particularly when compared to their group 11 counterparts, gold–NHCs (Au–NHC) and copper–NHCs (Cu–NHC). In this Special Issue on Featured Reviews in Organometallic Chemistry, we present a comprehensive overview of the application of silver–NHC complexes in the p-activation of alkynes. The functionalization of alkynes is one of the most important processes in chemistry, and it is at the bedrock of organic synthesis. Recent studies show the significant promise of silver–NHC complexes as unique and highly selective catalysts in this class of reactions. The review covers p-activation reactions catalyzed by Ag–NHCs since 2005 (the first example of p-activation in catalysis by Ag–NHCs) through December 2022. The review focuses on the structure of NHC ligands and p-functionalization methods, covering the following broadly defined topics: (1) intramolecular cyclizations; (2) CO2 fixation; and (3) hydrofunctionalization reactions. By discussing the role of Ag–NHC complexes in the p-functionalization of alkynes, the reader is provided with an overview of this important area of research and the role of Ag–NHCs to promote reactions that are beyond other group 11 metal–NHC complexes. [ABSTRACT FROM AUTHOR]

Nanocomposites constructed with heterostructures of graphitic carbon nitride (g-C3N4), silver (Ag), and titanium dioxide (TiO2) have emerged as promising nanomaterials for various environmental, energy, and clinical applications. In the field of textiles, Ag and TiO2 are already recognized as essential nanomaterials for the chemical surface and bulk modification of various textile materials, but the application of composites with g-C3N4 as a green and visible-light-active photocatalyst has not yet been fully established. This review provides an overview of the construction of Ag/g-C3N4, TiO2/g-C3N4, and Ag/TiO2/g-C3N4 heterostructures; the mechanisms of their photocatalytic activity; and the application of photocatalytic textile platforms in the photochemical activation of organic synthesis, energy generation, and the removal of various organic pollutants from water. Future prospects for the functionalization of textiles using g-C3N4-containing heterostructures with Ag and TiO2 are highlighted. [ABSTRACT FROM AUTHOR]

The paper presents the preliminary results of cellulose modification by ion implantation. Three types of ions were implanted, i.e., copper, zinc and silver with fluences of 5 × 1014 and 5 × 1015 cm−2, respectively. The acceleration voltage of the implanted ions was 30 kV. The ion penetration depth profiles showed differences, especially in the Cu and Ag cases, due to the different ion beams of these elements. The implantation of cellulose with ions clearly changed the wettability of the material surface in the direction of hydrophobicity. The impact of implantation on the growth of the cellulose surface by mold fungi was also noticeable. Only the silver ion implantation had a negative effect on the growth of the Trichoderma viride fungus but did not cause a complete inhibition of growth. Cellulose implantation with Cu and Zn ions clearly stimulated the growth of fungi on the surface of the polymer. [ABSTRACT FROM AUTHOR]

TaOx = 0.2Ny = 0.8 was reported previously to have the highest modulus (E), hardness (H), and H to E ratio attributed to the embedment of substituting oxygen atoms in the TaN crystal structure, among some TaOxNy coatings studied. In the present study, TaO0.2N0.8-Ag nanocomposite coatings were fabricated by reactive multi-target sputtering with O/N ratio adjusted to the expected value. The various Ag contents were doped to induce antibacterial behaviors. After deposition and annealing with rapid thermal process (RTP) at 400 °C for 4 min, the coatings' mechanical and structural properties were studied. After these examinations, the samples were then studied for their cell attachment, cell viability, and biocompatibility with 3-T-3 cells, as well as for their antibacterial behaviors against Escherichia coli. It appeared that hardness and crack resistance could be improved further with suitable amount of Ag doped to the coatings, followed by rapid thermal annealing treatment. The coating with 1.5 at. % Ag had the highest hardness and good H/E ratio. It was also found that the antibacterial efficiency of TaO0.2N0.8-Ag coatings could be much improved, comparing with that of TaO0.2N0.8 coatings. The antibacterial efficiency increased with the increased Ag contents. There was no negative effect of Ag on the biocompatibility of TaO0.2N0.8-Ag. Through the cell attachment and viability testing using MTT(3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay, it can be summarized that surface roughness could be the dominating factor for cell viability and attachment, which means the improvement of biocompatibility. Accordingly, the samples with 1.5 at. % and 11.0 at. % Ag show the best biocompatibility. The variation of surface roughness was affected by the incorporation of Ag and oxygen atoms after rapid thermal annealing. [ABSTRACT FROM AUTHOR]

A flexible thermoelectric device has been considered as a competitive candidate for powering wearable electronics. Here, we fabricated an n-type Ag2Se/Ag composite film on a flexible nylon substrate using vacuum-assisted filtration and a combination of cold and hot pressing. By optimising the Ag/Se ratio and the sequential addition and reaction time of AA, an excellent power factor of 2277.3 μW∙m−1 K−2 (corresponding to a ZT of ~0.71) at room temperature was achieved. In addition, the Ag2Se/Ag composite film exhibits remarkable flexibility, with only 4% loss and 10% loss in electrical conductivity after being bent around a rod of 4 mm radius for 1000 cycles and 2000 cycles, respectively. A seven-leg flexible thermoelectric device assembled with the optimised film demonstrates a voltage of 19 mV and a maximum power output of 3.48 μW (corresponding power density of 35.5 W m−2) at a temperature difference of 30 K. This study provides a potential path to design improved flexible TE devices. [ABSTRACT FROM AUTHOR]

Atomically precise metal nanoclusters are a new kind of nanomaterials that appeared in recent years; a pair of isomer nanoclusters have the same metal types, numbers of metal atoms, and surface-protected organic ligands but different metal atom arrangements. This article summarizes the structure features of isomer nanoclusters and concentrates on synthesis methods that could lead to isomer structure. The pairs of isomer inorganic nanoclusters' conversion to each other and their applications in catalyst and photoluminescence are also discussed. We found that the structure conversions are relevant to their stability. However, with the same molecule formulas, different atom arrangements significantly influence their performance in applications. Finally, the existing challenges and some personal perspectives for this novel field in the nano-science investigation are proposed. We hope this minireview can offer a reference for researchers interested in inorganic isomer nanoclusters. [ABSTRACT FROM AUTHOR]

Nanoparticles agglomerate easily because of their high surface energy, which seriously reduces their tribological properties as lubricant additives. In this work, the core-shell nanoparticles Ag@polydopamine (PDA) were successfully prepared by the self-oxidation of dopamine hydrochloride on the surface of Ag nanoparticles and the dispersion of Ag nanoparticles in PAO6 was improved to promote anti-wear behaviors. The tribological properties of Ag@PDA nanocomposites as additives in poly alpha olefin (PAO) oil were studied under different concentrations, pressure and speed conditions by UMT-5 tribometer. It was demonstrated that the strong electrostatic repulsion of the PDA structure made the Ag nanoparticles better dispersed in PAO oil, thus playing a better lubricating role. When the concentration of the modified nanoparticles was 0.25 wt%, the friction coefficient of the lubricating oil decreased by 18.67% and no obvious wear was observed on the friction pair surface. When the Ag@PDA content was higher than 0.25 wt%, the tribological performance of the lubricating oil was weakened, which may be due to excessive Ag@PDA acting as an abrasive on the friction surface, thereby increasing friction and wear. The friction coefficient of the lubricating oil containing Ag@PDA decreased with the increase in load, but hardly changed with the increase in frequency. [ABSTRACT FROM AUTHOR]

Numerous applications of silver nanoparticles (AgNPs), as well as the toxic effects of these particles on soil organisms and microorganisms, raise the question of how reasonable the entry of these nanoparticles into the environment is. Studying the behavior of these nanoparticles with soil organisms and also their effect on soil microorganisms may be the first step to finding out the answer. Structural and form differences in these nanoparticles for use in different conditions can change their behavior. The surface of these nanoparticles is covered with diverse coatings with differing surface charges affecting their fate in soil environments. Naturally, studying this aspect is essential to better understand how these particles impact the environment. In the present study, urease and dehydrogenase enzymes were used as soil health indicators to evaluate the effect of AgNPs and silver nitrate (AgNO3). In order to investigate the effect of surface charge, concentration, and exposure time, three concentration levels (5, 25, 125 mg/kg soil), three different types of charged coatings (citrate (Cit), polyvinylpyrrolidone (PVP) and polyethyleneimine (PEI)) were added to the soil as a treatment and the activities of dehydrogenase (as an indicator of overall microbial activity) and urease (indicator of nitrogen cycle) were measured at three times (1 h, 1 day and 90 days) after soil contamination. The results showed that with increasing the concentration of AgNO3 and AgNPs, the amount of dehydrogenase and urease activity decreased significantly. In the case of urease enzyme, nanoparticles with PEI coating (positive charge) had the greatest effect on reducing activity. In the case of dehydrogenase the opposite was true, and nanoparticles with Cit coating (negative charged) showed a greater inhibitory effect. With increasing incubation time, the amount of enzymatic activity of both types of enzymes showed less decrease, so that the greatest decrease in activity was in the first hour, then in the first day, and finally in 90 days. By comparing silver nitrate and nanoparticles it was found that the effect of AgNPs on enzymatic activity was greater than silver nitrate. [ABSTRACT FROM AUTHOR]

Novel cubic microstructures for the purposes of plasmonic Ag-based NPs were made using biological wastes produced from a microbial culture of Bacillus cereus (B. cereus) employing a bottom-up approach for the biosynthesis of metal-based nanomaterials. The unique surface plasmon resonance (SPR) of the as-prepared Ag-based NPs was detected at 405 nm. The infra-red spectrum revealed that the used biological waste effectively stabilized our Ag-based NPs. Scanning and transmission electron microscopes were used in order to evaluate the sizes and shapes of the distinctive structures present in our samples. The Ag NPs had a face-centered cubic structure, with a size of 64.4 nm for the (200) nano-crystallites, according to the X-ray diffraction that was conducted. The zeta potential was found to be −19.5 mV and the dynamic light scattering (DLS) size was 238.8 nm. Methylene blue's (MB) reaction with NaBH4 was used in order to measure the catalytic activity of the generated Ag-based NPs over a period of 1 to 5 min. With an astonishing reaction rate of 0.2861 min−1, the MB elimination percentage reached 67% in just 5 min, displaying outstanding catalytic activity. This work can therefore encourage the use of this biowaste for the ecologically benign, cost-effective, and long-term synthesis of innovative Ag-based nanoparticles and nanostructures, as well as in their use as catalysts in the catalytic reduction in MB. [ABSTRACT FROM AUTHOR]

Self-assembly of (Bu4N)4[β-Mo8O26], AgNO3, and 2-bis[(2,6-diisopropylphenyl)-imino]acenaphthene (dpp-bian) in DMF solution resulted in the (Bu4N)2[β-{Ag(dpp-bian)}2Mo8O26] (1) complex. The complex was characterized by single crystal X-ray diffraction (SCXRD), X-ray powder diffraction (XRPD), diffuse reflectance (DR), infrared spectroscopy (IR), and elemental analysis. Comprehensive SCXRD studies of the crystal structure show the presence of Ag+ in an uncommon coordination environment without a clear preference for Ag-N over Ag-O bonding. Quantum chemical calculations were performed to qualify the nature of the Ag-N/Ag-O interactions and to assign the electronic transitions observed in the UV–Vis absorption spectra. The electrochemical behavior of the complex combines POM and redox ligand signatures. Complex 1 demonstrates catalytic activity in the electrochemical reduction of CO2. [ABSTRACT FROM AUTHOR]

The increase in diesel consumption has led to the proliferation of soot particles from diesel exhaust, resulting in pollution in the form of smog. To solve this problem, a series of Ag-doped Mn1−xAgxCo2O4 spinel catalysts were successfully prepared using an auto-combustion synthesis method that uses glucose as a fuel. X-ray diffraction and Fourier transform infrared spectroscopy analysis were used to analyse the phase structure of the as-prepared samples. The results reveal that the selected catalysts featured a spinel-type structure. Moreover, the catalytic activity of the catalysts for soot combustion was evaluated by temperature-programmed reaction analysis. The temperature required for soot combustion depended heavily on the Ag concentration in the Mn1−xAgxCo2O4 catalyst. The Mn0.8Ag0.2Co2O4 catalyst had a superior catalytic activity with a T90 of 399 °C and CO2 selectivity of 99.3%. [ABSTRACT FROM AUTHOR]

This work examined the thermoluminescence dosimetry characteristics of Ag-doped ZnO thin films. The hydrothermal method was employed to synthesize Ag-doped ZnO thin films with variant molarity of Ag (0, 0.5, 1.0, 3.0, and 5.0 mol%). The structure, morphology, and optical characteristics were investigated using X-ray diffraction (XRD), scanning electron microscope (SEM), energy-dispersive X-ray spectroscopy (EDX), photoluminescence (PL), and UV–vis spectrophotometers. The thermoluminescence characteristics were examined by exposing the samples to X-ray radiation. It was obtained that the highest TL intensity for Ag-doped ZnO thin films appeared to correspond to 0.5 mol% of Ag, when the films were exposed to X-ray radiation. The results further showed that the glow curve has a single peak at 240–325 °C, with its maximum at 270 °C, which corresponded to the heating rate of 5 °C/s. The results of the annealing procedures showed the best TL response was found at 400 °C and 30 min. The dose–response revealed a good linear up to 4 Gy. The proposed sensitivity was 1.8 times higher than the TLD 100 chips. The thermal fading was recorded at 8% for 1 Gy and 20% for 4 Gy in the first hour. After 45 days of irradiation, the signal loss was recorded at 32% and 40% for the cases of 1 Gy and 4 Gy, respectively. The obtained optical fading results confirmed that all samples' stored signals were affected by the exposure to sunlight, which decreased up to 70% after 6 h. This new dosimeter exhibits good properties for radiation measurement, given its overgrowth (in terms of the glow curve) within 30 s (similar to the TLD 100 case), simple annealing procedure, and high sensitivity (two times that of the TLD 100). [ABSTRACT FROM AUTHOR]

A flexible and stretchable electrode based on polydimethylsiloxane (PDMS)-Ag nanosheet composite with low resistance and stable properties has been investigated. Under the synergistic effect of the excellent flexibility and stretchability of PDMS and the excellent electrical conductivity of Ag nanosheets, the electrode possesses a resistivity as low as 4.28 Ωm, a low resistance variation in the 0–50% strain range, a stable electrical conductivity over 1000 cycles, and a rapid recovery ability after failure caused by destructive large stretching. Moreover, the conductive mechanism of the flexible electrode during stretching is explained by combining experimental tests, theoretical models of contact point-tunneling effect, and finite element simulation. This research provides a simple and effective solution for the structure design and material selection of flexible electrodes, and an analytical method for the conductive mechanism of stretchable electrodes, which has potential for applications in flexible electronic devices, smart sensing, wearable devices, and other fields. [ABSTRACT FROM AUTHOR]

A competitive new technology, organic metallic halide perovskite solar cells feature a wide working area, low manufacturing costs, a long lifespan, and a significant amount of large efficacy of power conversion (PCE). The spin-coating technique was utilized for the fabrication of pure CH3NH3PbBr3 (MAPbBr3) thin films, and these films are implanted with 600 keV silver (Ag) ions at fluency rate of 6 × 1014 and 4 × 1014 ions/cm2. XRD analysis confirmed the cubic structure of MAPbBr3. A high grain size was observed at the fluency rate of 4 × 1014 ions/cm2. The UV-Vis spectroscopic technique was used to calculate the optical properties such as the bandgap energy (Eg), refractive index (n), extinction coefficients (k), and dielectric constant. A direct Eg of 2.44 eV was measured for the pristine film sample, whereas 2.32 and 2.36 eV were measured for Ag ion-implanted films with a 4 × 1014 and 6 × 1014 ions/cm2 fluence rate, respectively. The solar cells of these films were fabricated. The Jsc was 6.69 mA/cm2, FF was 0.80, Voc was 1.1 V, and the efficiency was 5.87% for the pristine MAPbBr3-based cell. All of these parameters were improved by Ag ion implantation. The maximum values were observed at a fluency rate of 4 × 1014 ions/cm2, where the Voc was 1.13 V, FF was 0.75, Jsc was 8.18 mA/cm2, and the efficiency was 7.01%. [ABSTRACT FROM AUTHOR]

A green synthesis of Ag/AgCl with an exceptional SPR and photocatalysis property is greatly benefit to the environmental application especially pollutant removal. In this work, a novel green plasmonic photocatalysis of Ag/AgCl nanocatalyst using aqueous garlic extract (Allium Sativum L.) was successfully synthesized. The allicin and organosulfur compounds in the garlic can act as reducing agents in the green synthesis process. The nanocatalyst properties were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray diffractometer. The light-harvesting property was investigated by UV-vis absorption spectra which reveals its visible light absorption capability owing surface plasmon resonance behavior of Ag nanoparticles. The degradation and mineralization of methylthioninium chloride (MC) using this photocatalyst were evaluated under visible light and natural solar irradiation. Surface plasmon resonance of Ag nanoparticles and the presence of organosulfur from the garlic extract facilitated adsorption of MC onto the particle surface, promoting greater degradation. The photocatalytic reaction under visible light can be explained by the pseudo first-order pattern with the highest reaction rate of 0.5829 mg L−1 min−1 at pH 10. The photocatalytic activity of the Ag/AgCl under the natural sunlight reached 90% and 75% for MC and total organic carbon (TOC), respectively. The intermediate products detected during MC degradation under sunlight irradiation before final transformation to CO2, H2O, HNO3, and H2SO4 were also reported. The simplicity of Ag/AgCl green synthesis with the photocatalysis properties under visible light and sunlight can offer the convenience of applying these nanoparticles for pollutant removal in water treatment processes. [ABSTRACT FROM AUTHOR]

Various studies have shown that the reproductive organs are highly sensitive to toxic elements found in the environment. Due to technological progress, the use of nanoparticles has become more common nowadays. Nanoparticles are used for drug delivery because their dimensions allow them to circulate throughout the body and enter directly into the cell. Antimicrobial properties are increasingly used in the manufacture of medical devices, textiles, food packaging, cosmetics, and other consumer products. Nanoparticles provide several benefits, but aspects related to their effects on living organisms and the environment are not well known. This review summarizes current in vivo, and in vitro animal studies focused on the evaluation of toxicity of selected metal nanoparticles (Ag, ZnO, TiO2) on male and female reproductive health. It can be concluded that higher concentrations of metal nanoparticles in the male reproductive system can cause a decrease in spermatozoa motility, viability and disruption of membrane integrity. Histopathological changes of the testicular epithelium, infiltration of inflammatory cells in the epididymis, and prostatic hyperplasia have been observed. Nanoparticles in the female reproductive system caused their accumulation in the ovaries and uterus. Metal nanoparticles most likely induce polycystic ovary syndrome and follicular atresia, inflammation, apoptosis, and necrosis also occurred. [ABSTRACT FROM AUTHOR]

A method for surface-enhanced Raman spectroscopy (SERS) sensing of polycyclic aromatic hydrocarbons (PAHs) is reported. Fe3O4@PDA@Ag@GO is developed as the SERS substrate prepared by classical electrostatic attraction method based on the enrichment of organic compounds by graphene oxide (GO) and polydopamine (PDA) and the good separation and enrichment function of Fe3O4. The morphology and structure of the SERS substrate were represented by transmission electron microscopy (TEM), energy-dispersive spectroscopy (EDS), X-ray diffraction (XRD) and the UV–visible absorption spectrum (UV–vis spectra). The effect of different temperatures on SERS during synthesis was investigated, and it was found that the best effect was achieved when the synthesis temperature was 90 °C. The effect of each component of Fe3O4@PDA@Ag@GO nanocomposites on SERS was explored, and it was found that Ag NPs are of great significance to enhance the Raman signal based on the electromagnetic enhancement mechanism; apart from enriching the polycyclic aromatic hydrocarbons (PAHs) through π–π interaction, GO also generates strong chemical enhancement to the Raman signal, and PDA can prevent Ag from shedding and agglomeration. The existence of Fe3O4 is favored for the fast separation of substrate from the solutions, which greatly simplifies the detection procedure and facilitates the cycle use of the substrate. The experimental procedure is simplified, and the substrate is reused easily. Three kinds of PAHs (phenanthrene, pyrene and benzanthene) are employed as probe molecules to verify the performance of the composite SERS substrate. The results show that the limit of detection (LOD) of phenanthrene pyrene and benzanthene detected by Fe3O4@PDA@Ag@GO composite substrate are 10−8 g/L (5.6 × 10−11 mol/L), 10−7 g/L (4.9 × 10−10 mol/L) and 10−7 g/L (4.4 × 10−10 mol/L), respectively, which is much lower than that of ordinary Raman, and it is promising for its application in the enrichment detection of trace PAHs in the environment. [ABSTRACT FROM AUTHOR]

ZnO and hybrid of ZnO/Ag structures in the nanometer size were electroless deposited on the Mg-Ca0.3 alloy surface, achieved from aqueous solutions (10−3 M at 21 °C) of ZnO (suspension), Zn(NO3)2 and AgNO3. The surface characterization of the deposits was carried out by Scanning Electron Microscopy-Energy Dispersive Spectroscopy (SEM-EDS), X-Ray Photoelectron Spectroscopy (XPS), Fourier transform infrared (FTIR), UV-Visible and Raman spectroscopy. The nanoparticles (NPs) area size distribution analysis revealed that the average of ZnO-NPs was ~85 nm. Likewise, the Ag-NPs of electroless deposits had an average area size of ~100 nm and nucleated in the vicinity of ZnO-NPs as Ag+ ions have been attracted by the negatively charged O2− atoms of the Zn-O dipole. The ZnO-NPs had the wurtzite structure, as indicated by Raman spectroscopy analysis and XRD complementary analysis. The UV-Visible spectroscopy analysis gave a peak at ~320 nm associated with the decrease in the imaginary part (k) of the refractive index of Ag-NPs. On the Mg-Ca0.3 surface, MgO, Mg(OH)2 and MgCO3 are present due to the Mg-matrix. XRD spectra of Ag-NPs indicated the presence of planes arranged with the FCC hexagonal structure. The reported hybrid ZnO/Ag electroless deposits of NPs are of interest for temporary implant devices, providing antibacterial properties to Mg-Ca0.3 surface, a widely used biodegradable material. [ABSTRACT FROM AUTHOR]

The paper presented the mechanical (MChT), microwave (MWT), and hydrothermal (HTT) methods of zirconium phosphate samples modification in order to improve its adsorption affinity for the Ag (I) ions. The FTIR studies proved that the modification of both gel and xerogel samples with the ultrasonic microwaves causes an increase in the concentration of phosphate groups on the surface of MWT-modified zirconium phosphate: the isoelectric point pHiep = 2.2–2.9 for these samples against 3.9 for the initial sample and pKa2 values were 4.7–5.6 and 6.3, respectively. As resulting from the Ag+ ion adsorption studies, the MWT treatment of zirconium phosphate samples caused the greatest affinity of Ag+ ions for the surface of MWT zirconium phosphate. Compared with the initial ZrP sample, the shift of the Ag (I) ion adsorption edge towards lower pH values was observed, e.g., with adsorption of Ag (I) ions from the solution with the initial concentration of 1 µmol/dm3 for the initial ZrP sample pH50% = 3.2, while for the sample MWT ZrPxero pH50% = 2.6. [ABSTRACT FROM AUTHOR]

Visible-light-driven heterostructure Ag/Bi2WO6 nanocomposites were prepared using a hydrothermal method followed by the photodeposition of Ag on Bi2WO6. A photocatalyst with a different molar ratio of Ag to Bi2WO6 (1:1, 1:2 and 2:1) was prepared. The catalytic performance of Ag/Bi2WO6 towards the photocatalytic oxidation of rhodamine B (RhB) and methylene blue (MB) was explored. Interestingly, the Ag/Bi2WO6 (1:2) catalyst exhibited superior performance; it oxidized 83% of RhB to Rh-110 and degraded 68% of MB in 90 min. This might be due to the optimum amount of Ag nanoparticles, which supported the rapid generation and transfer of separated charges from Bi2WO6 to Ag through the Schottky barrier. An excess of Ag on Bi2WO6 (1:1 and 2:1) blocked the active sites of the reaction and did not produce the desired result. The introduction of Ag on Bi2WO6 improved the electrical conductivity of the composite and lowered the recombination rate of charge carriers. Our work provides a cost-effective route for constructing high-performance catalysts for the degradation of toxic dyes. [ABSTRACT FROM AUTHOR]

Nanoparticles exhibiting the localized surface plasmon resonance (LSPR) phenomenon are promising tools for diagnostics and cancer treatment. Among widely used metal nanoparticles, silver nanoparticles (Ag NPs) possess the strongest light scattering and surface plasmon strength. However, the therapeutic potential of Ag NPs has until now been underestimated. Here we show targeted photothermal therapy of solid tumors with 35 nm HER2-targeted Ag NPs, which were produced by the green synthesis using an aqueous extract of Lavandula angustifolia Mill. Light irradiation tests demonstrated effective hyperthermic properties of these NPs, namely heating by 10 °C in 10 min. To mediate targeted cancer therapy, Ag NPs were conjugated to the scaffold polypeptide, affibody ZHER2:342, which recognizes a clinically relevant oncomarker HER2. The conjugation was mediated by the PEG linker to obtain Ag-PEG-HER2 nanoparticles. Flow cytometry tests showed that Ag-PEG-HER2 particles successfully bind to HER2-overexpressing cells with a specificity comparable to that of full-size anti-HER2 IgGs. A confocal microscopy study showed efficient internalization of Ag-PEG-HER2 into cells in less than 2 h of incubation. Cytotoxicity assays demonstrated effective cell death upon exposure to Ag-PEG-HER2 and irradiation, caused by the production of reactive oxygen species. Xenograft tumor therapy with Ag-PEG-HER2 particles in vivo resulted in full primary tumor regression and the prevention of metastatic spread. Thus, for the first time, we have shown that HER2-directed plasmonic Ag nanoparticles are effective sensitizers for targeted photothermal oncotherapy. [ABSTRACT FROM AUTHOR]

This work aims to define the microstructure and to study the mechanical properties of an Al matrix incorporated with various amounts of Fe2O3 (3, 6, 9, 12 and 15 wt.%) with a constant amount of Ag at 1 wt.%. Al/Fe2O3 + Ag hybrid nano-composite samples are manufactured using powder metallurgy. An aluminum matrix is considered an important alloy, owing to its properties such as being lightweight, strong and corrosion and wear resistant, which enable it to be used in many applications, such as electronics, aerospace and automotive purposes. Various examinations have been performed for the samples of this work, such as Field Emission Scanning Electron Microscopy (FESEM) and X-ray Diffraction (XRD) analysis to estimate the microstructure and phases of manufactured nano-composites. Mechanical testing is also carried out, such as micro-hardness testing, compressive testing and wear testing, to estimate the mechanical properties of the hybrid nano-composites. The results of FESEM and XRD demonstrate that Fe2O3 and Ag nanoparticles are uniformly distributed and dispersed into the Al matrix, whereas the mechanical tests show that enhancement t micro-hardness, compressive strength of 12 wt.% Fe2O3 + 1Ag and wear rate decrease to a minimum value of 12 wt.% of Fe2O3 + 1Ag. [ABSTRACT FROM AUTHOR]

Featured Application: Heterogeneous nanoparticles can be applied in optoelectronics (as catalysts) and drug delivery systems. For bioengineering, living cells can be subjected to photothermal therapy using them (AgPd/AuPd). These heterosynthetic nanoparticles can enhance therapeutic efficiency. Heterogeneous Ag/Au nanoparticles combined with Pd ions were generated by irradiating Ag/Au metal targets in a Pd solution with nanosecond and femtosecond lasers. AgPd and AuPd nanoparticles were generated by laser fragmentation and bonded. We numerically analyzed the hot spots with electromagnetic field enhancement of nanoparticles of different sizes separated by various distances. AgPd and AuPd nanoparticles differing in diameter were generated and showed different characteristics compared to typical core-shell heterogeneous nanoparticles. Pd ions played an important role in the generation of nanoparticles in liquid via laser ablation. The femtosecond laser produced both pure and heterogeneous nanoparticles of uniform size. The nanosecond laser produced pure nanoparticles with a relatively non-uniform size, which developed into spherical heterogeneous nanoparticles with a uniform (small) size in the presence of Pd ions. These nanoparticles could optimize applications such as photothermal therapy and catalysis. [ABSTRACT FROM AUTHOR]

Silver particles were prepared by dewetting Ag films coated on glass using a fiber laser. The size of the particles was controlled in the range of 92 nm–1.2 μm by adjusting the thickness of the Ag film. The structural properties and surface roughness of the particles were evaluated by means of scanning electron microscopy. In addition, the antifungal activity of the Ag particles was examined using spore suspensions of Colletotrichumgloeosporioides. It is shown that particles with a size of 1.2 μm achieved 100% inhibition of conidia growth of C.gloeosporioides after a contact time of just 5 min. Furthermore, the smaller particles also achieved good antifungal activity given a longer contact time. Similar results were observed for spore germination and pathogenicity tests performed on mango fruit and leaves. Overall, the results confirm that Ag particles have an excellent antifungal effect on C. gloeosporioides. [ABSTRACT FROM AUTHOR]

Many elements have been used as dopants to enhance the thermoelectric performance of Bi2Te3-related materials. Among them, Ag’s effect on thermoelectric properties, where Ag acts as a donor or acceptor, remains unclear. To elucidate the role of Ag in n-type Bi2Te3 based compounds, Ag was added to n-type (Bi0.9Sb0.1)2(Te0.85Se0.15)3. As the amount of Ag was increased, the electron concentration decreased, which means Ag acted as an acceptor. The added Ag atoms were found to occupy interstitial sites in the hexagonal lattices, as confirmed by X-ray analysis and first principles calculations. The reduction in electron concentration was attributed to the interaction between the interstitial Ag and intrinsic defects. [ABSTRACT FROM AUTHOR]

This article explains the mechanism of the metal/oxide core-shell Ag/TiO 2 and Au/TiO 2 nanoparticle formation via one-step ultrasonic spray pyrolysis (USP) by establishing a new model. The general knowledge on the standard "droplet-to-particle" (DTP) mechanism, nucleation, and growth processes of noble metals, as well as physical and chemical properties of core and shell materials and experimental knowledge, were utilized with the purpose of the construction of this new model. This hypothesis was assessed on silver (Ag)/titanium oxide (TiO 2) and gold (Au) TiO 2 binary complex nanoparticles' experimental findings revealed by scanning electron microscopy (SEM), focused ion beam (FIB), high-resolution transmission electron microscopy (HRTEM), and simulation of crystal lattices. It was seen that two mechanisms run as proposed in the new model. However, there were some variations in size, morphology, and distribution of Ag and Au through the TiO 2 core particle and these variations could be explained by the inherent physical and chemical property differences of Ag and Au. [ABSTRACT FROM AUTHOR]

We investigated the structural, optical, and electrical properties of amorphous IGZO/silver/amorphous IGZO (α-IGZO/Ag/α-IGZO) triple-layer structures that were deposited at room temperature on Eagle XG glass and flexible polyethylene terephthalate substrates through the sputtering method. Thin Ag layers with different thicknesses were inserted between two IGZO layers to form a triple-layer structure. Ag was used because of its lower absorption and resistivity. Field emission scanning electron microscopy measurements of the triple-layer structures revealed that the thicknesses of the Ag layers ranged from 13 to 41 nm. The thickness of the Ag layer had a large effect on the electrical and optical properties of the electrodes. The optimum thickness of the Ag metal thin film could be evaluated according to the optical transmittance, electrical conductivity, and figure of merit of the electrode. This study demonstrates that the α-IGZO/Ag/α-IGZO triple-layer transparent electrode can be fabricated with low sheet resistance (4.2 Ω/□) and high optical transmittance (88.1%) at room temperature without postannealing processing on the deposited thin films. [ABSTRACT FROM AUTHOR]

Ti and its alloys are the most commonly-used materials for biomedical applications. However, bacterial infection after implant placement is still one of the significant rising complications. Therefore, the application of the antimicrobial agents into implant surfaces to prevent implant-associated infection has attracted much attention. Scientific papers have shown that inorganic antibacterial metal elements (e.g., Ag, Cu, Zn) can be introduced into implant surfaces with the addition of metal nanoparticles or metallic compounds into an electrolyte via micro-arc oxidation (MAO) technology. In this review, the effects of the composition and concentration of electrolyte and process parameters (e.g., voltage, current density, oxidation time) on the morphological characteristics (e.g., surface morphology, bonding strength), antibacterial ability and biocompatibility of MAO antimicrobial coatings are discussed in detail. Anti-infection and osseointegration can be simultaneously accomplished with the selection of the proper antibacterial elements and operating parameters. Besides, MAO assisted by magnetron sputtering (MS) to endow Ti-based implant materials with superior antibacterial ability and biocompatibility is also discussed. Finally, the development trend of MAO technology in the future is forecasted. [ABSTRACT FROM AUTHOR]

Due to their peculiar qualities, metal-based nanostructures have been extensively used in applications such as catalysis, electronics, photography, and information storage, among others. New applications for metals in areas such as photonics, sensing, imaging, and medicine are also being developed. Significantly, most of these applications require the use of metals in the form of nanostructures with specific controlled properties. The properties of nanoscale metals are determined by a set of physical parameters that include size, shape, composition, and structure. In recent years, many research fields have focused on the synthesis of nanoscale-sizedmetallicmaterials with complex shape and composition in order to optimize the optical and electrical response of devices containing metallic nanostructures. The present paper aims to overview the most recent results--in terms of fabrication methodologies, characterization of the physico-chemical properties and applications--of complex-morphology metal-based nanostructures. The paper strongly focuses on the correlation between the complex morphology and the structures' properties, showing how the morphological complexity (and its nanoscale control) can often give access to a wide range of innovative properties exploitable for innovative functional device production. We begin with an overview of the basic concepts on the correlation between structural and optical parameters of nanoscale metallic materials with complex shape and composition, and the possible solutions offered by nanotechnology in a large range of applications (catalysis, electronics, photonics, sensing). The aim is to assess the state of the art, and then show the innovative contributions that can be proposed in this research field. We subsequently report on innovative, versatile and low-cost synthesis techniques, suitable for providing a good control on the size, surface density, composition and geometry of the metallic nanostructures. The main purpose of this study is the fabrication of functional nanoscale-sized materials, whose properties can be tailored (in a wide range) simply by controlling the structural characteristics. The modulation of the structural parameters is required to tune the plasmonic properties of the nanostructures for applications such as biosensors, opto-electronic or photovoltaic devices and surface-enhanced Raman scattering (SERS) substrates. The structural characterization of the obtained nanoscale materials is employed in order to define how the synthesis parameters affect the structural characteristics of the resulting metallic nanostructures. Then, macroscopic measurements are used to probe their electrical and optical properties. Phenomenological growth models are drafted to explain the processes involved in the growth and evolution of such composite systems. After the synthesis and characterization of the metallic nanostructures, we study the effects of the incorporation of the complex morphologies on the optical and electrical responses of each specific device. [ABSTRACT FROM AUTHOR]

FePt-Ag nanocomposite films with large perpendicular magnetic anisotropy have been fabricated by alternate-atomic-layer electron beam evaporation onto MgO(100) substrates at the low temperature of 300 °C. Their magnetization behavior and microstructure have been studied. The surface topography was observed and varied from continuous to nanogranular microstructures with insertion of Ag nanolayers into Fe/Pt bilayer films. The measurement of angular-dependent coercivity showed a tendency of the domain-wall motion as a typical peak behavior shift toward more like a coherent Stoner-Wohlfarth rotation type with the insertion of Ag nanolayers into the FePt films. On the other hand, the inter-grain interaction was determined from a Kelly-Henkel plot. The FePt film without insertion of Ag nanolayers has a positive M, indicating strong exchange coupling between neighboring grains, whereas the FePt film with insertion of Ag nanolayers has a negative M, indicating that inter-grain exchange coupling is weaker, thus leading to the presence of dipole interaction in the FePt-Ag nanogranular films. The magnetic characteristic measurements confirmed that the perpendicular magnetization reversal behavior and related surface morphology of low-temperature-ordered FePt(001) nanogranular films can be systematically controlled by the insertion of Ag nanolayers into the FePt system for next generation magnetic storage medium applications. [ABSTRACT FROM AUTHOR]

Plasmonic gas sensors are optical sensors that use localized surface plasmons or extended surface plasmons as transducing platform. Surface plasmons are very sensitive to dielectric variations of the environment or to electron exchange, and these effects have been exploited for the realization of sensitive gas sensors. In this paper, we review our research work of the last few years on the synthesis and the gas sensing properties of sol-gel based nanomaterials for plasmonic sensors. [ABSTRACT FROM AUTHOR]

Silver (Ag) nanomaterials are increasingly used in a variety of commercial applications. This study examined the effect of size (20 and 110 nm) and surface stabilization (citrate and PVP coatings) on toxicity, particle uptake and NLRP3 inflammasome activation in a variety of macrophage and epithelial cell lines. The results indicated that smaller Ag (20 nm), regardless of coating, were more toxic in both cell types and most active in the THP-1 macrophages. TEM imaging demonstrated that 20 nm Ag nanospheres dissolved more rapidly than 110 nm Ag nanospheres in acidic phagolysosomes consistent with Ag ion mediated toxicity. In addition, there were some significant differences in epithelial cell line in vitro exposure models. The order of the epithelial cell lines' sensitivity to Ag was LA4 > MLE12 > C10. The macrophage sensitivity to Ag toxicity was C57BL/6 AM > MARCO null AM, which indicated that the MARCO receptor was involved in uptake of the negatively charged Ag particles. These results support the idea that Ag nanosphere toxicity and NLRP3 inflammasome activation are determined by the rate of surface dissolution, which is based on relative surface area. This study highlights the importance of utilizing multiple models for in vitro studies to evaluate nanomaterials. [ABSTRACT FROM AUTHOR]