Silver nanoparticles deposited on porous silicon as a surface-enhanced Raman scattering (SERS) active substrate

Silver nanoparticles were deposited spontaneously from their aqueous solution on a porous silicon (PS) layer. The PS acts both as a reducing agent and as the substrate on which the nanoparticles nucleate. At higher silver ion concentrations, layers of nanoparticle aggregates were formed on the PS surface. The morphology of the metallic layers and their SERS activity were influenced by the concentrations of the silver ion solutions used for deposition. Raman measurements of rhodamine 6G (R6G) and crystal violet (CV) adsorbed on these surfaces showed remarkable enhancement of up to about 10 orders of magnitude.     

The segregation of silver nanoparticles in low-cost ceramic water filters

As an impregnated constituent in low-cost ceramic water filters, silver nanoparticles have a demonstrated antibacterial effect. The bactericidal mechanism is believed to be based on direct contact between silver and the cell wall of a contaminant organism. In this study microstructural analysis was used to examine the effect of the processing method on the distribution of silver nanoparticles in the filter material. Silver nanofluid was impregnated into fired clay ceramic samples by a low-cost soak-and-dry method. Analyses of filter samples by scanning electron microscopy, energy dispersive spectroscopy, and digital optical topological mapping showed that silver was concentrated in near surface pores, a condition that is not optimal for highest probability of silver contact. A simple experiment showed that segregation of silver occurs during the drying phase of impregnation. Drying curves showed that 90% of contained liquid evaporates from the external surface.     

载Ag/Cu纳米粒子多孔聚丙烯腈复合纤维膜的制备及其抑菌性

金属纳米粒子因其独特的物理化学性能,在催化、抑菌、水污染处理和生物医学等领域表现出巨大的应用前景。但是金属纳米粒子在制备和使用过程中容易发生团聚而影响其性能。因此,提高金属纳米粒子的稳定性,对提升其应用性能具有重大意义。本文在以聚丙烯腈(PAN)为基体,聚乙烯吡咯烷酮(PVP)为致孔剂,基于静电纺丝技术制得多孔聚丙烯腈纳米纤维(PPAN NFs)的基础上,通过浸渍沉积法分别制备出负载银纳米粒子(Ag NPs)复合纳米纤维(Ag-PPAN NFs)和负载铜纳米粒子(Cu NPs)复合纳米纤维(Cu-PPAN NFs)。在利用FESEM、EDS、XRD等方法对制备纤维膜的形貌和结构进行表征的基础上,通过抑菌圈法和FESEM观察经复合纳米纤维处理前后的细菌形貌来研究Ag-PPAN NFs和Cu-PPAN NFs对大肠杆菌、金黄色葡萄球菌和白色念球菌的抑菌性能。研究结果发现：PPAN NFs可有效解决Ag NPs和Cu NPs在制备和使用过程中易于聚集的问题,制得的复合纳米纤维对大肠杆菌、金黄色葡萄球菌和白色念球菌具有一定的抗菌活性,可成为一种新型的抗菌纤维材料。     

Synthesis and characterization of silver nanoparticles and their antimicrobial efficacy

An efficient protocol for synthesis of silver nanoparticles (AgNPs) using the combination of aqueous extract of Tinospora cordifolia leaves and 5 mM silver nitrate (AgNO₃) solution was developed. This study revealed that bioactive compounds present in the extract function as stabilizing and capping agent for AgNPs. Scanning electron microscope and transmission electron microscope studies confirm the structure and surface morphology of the AgNPs. The size of synthesized AgNPs was in the range of 30–50 nm having spherical morphology. The crystalline nature of NPs was defined by the X-ray diffraction pattern. The AgNPs were found to be toxic against pathogenic bacteria such as Escherichia coli (ATCC 25922), Pseudomonas aeruginosa (ATCC 27853), and Staphylococcus aureus (ATCC 29213) and against plant pathogenic fungi Fusarium oxysporum (MTCC 8608) and Sclerotinia sclerotiorum (MTCC 8785). The use of AgNPs as antibacterial and antifungal agent is advantageous over other methods for control of pathogenic microorganisms, and it can be of great importance in developing novel drugs for curing many lethal diseases.     

Layer-by-layer deposition of green synthesised silver nanoparticles on polyester air filters and its antimicrobial activity

Silver nanoparticles stabilised with anionic polymeric polyelectrolytes were successfully synthesised by high-energy UV reduction. Three types of polyelectrolytes were used including poly(methacrylic acid) (PMA), poly(acrylic acid) (PAA) and poly(4-styrenesulphonic acid-co-maleic acid) (CoPSS). The formation of the prepared solutions exhibited surface plasmon resonance at the wavelength of 475, 730 and 408 nm by using PMA, PAA and CoPSS as the stabilising agents. UV–visible spectrophotometer, transmission electron microscope (TEM) and zeta potential analyser were employed to characterise the formation of the prepared solutions. The silver nanoparticles stabilised with anionic polyelectrolytes were immobilised on polyester air filters using a layer-by-layer technique. This is the sequential dipping of polyester air filters in a dilute solution of cationic poly(diallyldimethylammonium chloride) and anionic polymeric polyelectrolytes capped silver. The surface topography of the polyester air filters were measured by field emission scanning electron microscope. Results showed that silver nanoparticles had the highest surface coverage on the polyester air filters probably because it is a good bonding candidate and insures strong film growth. The multilayers polyester air filters coated silver nanoparticles were tested against the gram positive pathogen Staphylococcus aureus. The deposition of silver nanoparticles onto the polyester air filters resulted in 92.18%, 84.32% and 71.19% of bacteria removal using PMA, PAA and CoPSS as the stabilising agent.     

Ultrasensitive multiplexed immunoassay with electrochemical stripping analysis of silver nanoparticles catalytically deposited by gold nanoparticles and enzymatic reaction

A novel ultrasensitive multiplexed immunoassay method was developed by combining alkaline phosphatase (ALP)-labeled antibody functionalized gold nanoparticles (ALP-Ab/Au NPs) and enzyme-Au NP catalyzed deposition of silver nanoparticles at a disposable immunosensor array. The immunosensor array was prepared by covalently immobilizing capture antibodies on chitosan modified screen-printed carbon electrodes. After sandwich-type immunoreactions, the ALP-Ab/Au NPs were captured on an immunosensor surface to catalyze the hydrolysis of 3-indoxyl phosphate, which produced an indoxyl intermediate to reduce Ag(+). The silver deposition process was catalyzed by both ALP and Au NPs, which amplified the detection signal. The deposited silver was then measured by anodic stripping analysis in KCl solution. Using human and mouse IgG as model analytes, this multiplexed immunoassay method showed wide linear ranges over 4 orders of magnitude with the detection limits down to 4.8 and 6.1 pg/mL, respectively. Acceptable assay results for practical samples could be obtained. The newly designed strategy avoided cross talk and the need of deoxygenation for the electrochemical immunoassay and, thus, provided a promising potential in clinical applications.     

Formation of silver nanoparticles in poly(perfluorosulfonic) acid membrane

The formation of silver nanoparticles by chemical reduction of Ag+-loaded Nafion-117 membrane with NaBH4 was studied using radioactivity tagged ions. The counterion-exchange method (Ag(m)+ <--> Na(s)+) was used to obtain a membrane sample with a varying proportion of Ag+ ions. The X-ray elemental mapping across the thickness of the membrane by energy-dispersive X-ray spectrometer attached to the environmental scanning electron microscope (ESEM/EDAX) indicated that Na+ and Ag+ were uniformly distributed in the membrane samples before reduction. The average size of nanoparticles formed after reduction was found to be 15 +/- 3 nm, irrespective of the concentration of silver ions present in the membrane before reduction. Energy-dispersive X-ray fluorescence (EDXRF) analyses of the membrane samples, carried out before and after reduction, indicated that the Ag concentration on the membrane surface was considerably increased after reduction. EDXRF measurements of the membrane samples, obtained from reduction carried out in a dead end cell, indicated that Ag nanoparticles were formed only on the membrane surface exposed to NaBH4 solution. Reduction carried out with NaBH4 tagged with 22Na showed that the formation of Ag nanoparticles involved exchange of Ag+ ions from ion-exchange sites in the interior of the membrane with Na+ ions, followed by reduction of Ag+ ions with BH4- ions at the surface of membrane. The study of self-diffusion of water, Na+, and Cs+ ions in the membrane loaded with Ag nanoparticles indicated that formation of Ag nanoparticles did not affect the diffusional transport properties of the membrane. The ion-exchange capacity and water uptake capacity were also not affected by the formation of Ag nanoparticles in the membrane. The spatial distribution of Ag nanoparticles across the thickness of the membrane obtained by ESEM/EDAX showed that Ag nanoparticles were confined to a few-micrometer surface layer of the membrane. Based on these observations, an attempt has been made to explain the mechanism of the formation of Ag nanoparticles in the membrane.     

In situ growth of silver nanoparticles in porous membranes for surface-enhanced raman scattering

We demonstrate the in situ growth of silver nanoparticles in porous alumina membranes (PAMs) for use as a surface-enhanced Raman scattering (SERS) detection substrate. This fabrication method is simple, cost-effective, and fast, while providing control over the size of silver nanoparticles through the entire length of the cylindrical nanopores with uniform particle density inside the pores unachievable by the traditional infiltration technique. The in situ growth of silver nanoparticles was conducted from electroless-deposited nanoscale seeds on the interior of the PAM and resulted in the formation of numerous hot spots, which facilitated significantly higher SERS enhancement for these substrates compared with previously reported porous substrates.     

Evaluation of the wound healing efficacy of chemical and phytogenic silver nanoparticles

Wound healing requires a series of cellular events and a cascade of co‐ordinated and systemic biochemical events. Silver nanoparticles possess many beneficial properties for wound management including antibacterial, anti‐inflammatory and pro‐healing properties. In this study, the authors investigated the wound healing properties of Cinnamomum verum extract mediated nanosilver (CENS) particles in comparison with 1% povidone iodine, citrate mediate NS and CE treatments. The topical application of CENS showed good antibacterial activity and accelerated wound healing with complete epithelialisation and normal re‐growth of hair in all three models of study: namely, excision, incision and dead space models in rats compared with all other treatments. CENS was also found to promote collagen synthesis, stabilise wound besides countering oxidative stress and stimulating cellular proliferation CENS could be a novel therapeutic agent for wound management.Inspec keywords: silver, nanoparticles, nanomedicine, wounds, antibacterial activity, biomedical materials, biochemistry, cellular biophysics, proteinsOther keywords: wound healing efficacy, chemical nanoparticles, phytogenic silver nanoparticles, cellular events, systemic biochemical events, wound management, antibacterial properties, anti‐inflammatory properties, pro‐healing properties, Cinnamomum verum extract mediated nanosilver particles, CENS, complete epithelialisation, normal hair regrowth, excision model, incision model, dead space model, rats, collagen synthesis, oxidative stress, cellular proliferation, therapeutic agent, Ag     

Optical properties of porous anodic alumina membrane uniformly decorated with ultra-thin porous gold nanoparticles arrays

In this paper, we directly develop a facile method to decorate a modified porous anodic alumina membrane (PAA) with an ultrathin porous film of gold nanoparticles with sub-gaps less than 25 nm and particle size less than 40 nm on the top surface and Au nanoparticles uniformly attached to the pore walls as well as the bottom of the pores, utilizing radio-frequency magnetron sputtering. The size as well as the interparticle distance of the gold nanostructures is adjusted by changing the structural properties of PAA membrane and the sputtering time. According to the measured reflection spectra, the saturation of interference color is significantly enhanced. As a result, the Au-coated PAA membrane exhibits a brilliant and tunable color. Field enhancement can be achieved in these structures through the excitation and constructive interference of surface plasmon waves. In addition, the role of localized surface plasmon and propagating surface plasmon was discussed. A four-layered model is presented to describe the reflectance data that show excellent agreement with the experimental data. The brilliant Au-coated PAA membrane is useful for decorative purposes and holds promise as an effective surface enhanced Raman scattering (SERS) substrate.     

Reflectivity spectra and colors of porous anodic aluminum oxide containing silver nanoparticles by plasmonic absorption

The reflectivity spectra and color of porous anodic aluminum oxide (AAO) nanostructures containing the assembly of silver (Ag) nanoparticles (NPs) with a diameter of -10 nm were investigated. The Ag NPs were assembled inside the pores of AAO with a diameter of -60 nm by dip-coating process during which Ag NPs adsorbed on the surface of AAO and driven inside the pores by capillary force upon the evaporation of solvent. The reflectivity spectra and associated colors of AAO with Ag NPs were determined by the plasmonic absorption of light by Ag NPs. Even with the monolayer coverage of Ag NPs in the pores of AAO, the reflectivity is significantly reduced specifically at -465 nm wavelength by a strong plasmonic absorption, resulting in its golden color. Aggregating Ag NPs by post-annealing at 300 and 400 degrees C changed the color to pink due to the red-shift of absorption. These results are indicative of potential color-engineering of NPs/AAO platform by wavelength-selective reduction of reflected light intensity and using it in direct optical read-out of change of surface and morphology conditions.     

Bacteriocin‐capped silver nanoparticles for enhanced antimicrobial efficacy against food pathogens

Bacteriocins produced by lactic acid bacteria are safer alternatives to the more popularly used chemical preservatives which exhibit several adverse effects. The bacteriocins have an advantage of being efficient in controlling food pathogens without possessing any side‐effects. However, the bacteriocins have a limitation of exhibiting a narrow antimicrobial spectrum and having a high‐dosage requirement. With an aim to combat these limitations, the present study involved the biosynthesis of bacteriocin‐capped nanoparticles, using two bacteriocins (Bac4463 and Bac22) extracted and purified from Lactobacillus strains. Nanoconjugates synthesised at optimum conditions were characterized using various physico‐chemical techniques. The interaction of bacteriocin‐capped silver nanoparticles with the pathogenic bacteria was observed using scanning electron microscopy, wherein the deformed and elongated cells were clearly visible. In vitro antimicrobial efficacy of both Bac4463‐capped silver nanoparticles and Bac22‐capped silver nanoparticles against different food pathogens was observed to be enhanced in comparison to the antimicrobial activity of bacteriocins alone. Minimum inhibitory concentration was observed to be as low as 8 μg/ml for Bac4463‐capped silver nanoparticles against Staphylococcus aureus, and 2 μg/ml for Bac22‐capped silver nanoparticles against Shigella flexneri. This study, therefore, recommends the use of bacteriocin‐capped nanoparticles as food preservatives to control the growth of food spoiling bacteria.Inspec keywords: preservatives, elongation, food safety, silver, biotechnology, antibacterial activity, food preservation, nanoparticles, nanofabrication, food products, scanning electron microscopy, microorganismsOther keywords: bacteriocins, chemical preservatives, food pathogens, bacteriocin‐capped nanoparticles, bacteriocin‐capped silver nanoparticles, Bac4463‐capped silver nanoparticles, Bac22‐capped silver nanoparticles, enhanced antimicrobial efficacy     

Oxidation of evaporated porous silicon rugate filters

Rugate filters are thin-film optical interference coatings with sinusoidal variation of the refractive index. Several of these filters were fabricated with glancing angle deposition, which exploits atomic competition during growth to create nanoporous materials with controllable effective refractive index. This method enables the fabrication of devices with almost arbitrary refractive index profiles varying between the ambient, 1.0, and the index of the film material, in this case silicon with an index of 4.0 (at 600 nm). As these filters are inherently porous, oxidation of the silicon can occur throughout the device layer, and here we study the intentional oxidation of silicon filters by high-temperature reaction with gaseous oxygen. We find that a significant portion of the silicon filter oxidizes in approximately 10 min when heated to 600 degrees C-650 degrees C in an oxygen environment; oxidation then continues slowly over several hours. The presence of water vapor has little apparent effect on the oxidation reaction, and attempts to oxidize with ozone at room temperature were unsuccessful. As silicon filters oxidize to become silica, spectral blueshifts and increased short-wavelength transmittance are observed. Measured and calculated transmittance spectra generally agree, although the lack of absorption and dispersion in the theoretical model limits detailed comparison.     

Functionalization of ordered iron-based nanoparticles deposited on mesoporous films

Mesoporous films obtained by dip-coating, combining polycondensation of silicate species and organization of amphiphilic mesophases, were decorated with iron-based nanoparticles from iron aqueous solution. High-resolution transmission electron microscopy (HR-TEM) images and energy dispersive X-rays spectroscopy (EDS) analysis show that the nanoparticles have diameters between 5 to 10 nm and they are deposited in an ordered sequence exclusively on top of the mesoporous structure. Afterward, by irradiating the material with a hydrogen ion beam, the iron-based compound is functionalized, i.e., its physical-chemical properties are modified. X-ray photoelectron spectroscopy (XPS) showed that the iron oxides and hydroxides are reduced to metallic iron. The deposition of organized iron-based nanoparticles and further ion beam functionalization might open perspectives on the study and fabrication of complex new materials.     

TEM observation of gold nanoparticles deposited on cerium oxide

The structure of Au nanoparticles supported on CeO₂ using the deposition precipitation method was observed using a transmission electron microscope (TEM). The shape of Au nanoparticles and the fine structure of contact interface between the Au nanoparticles and CeO₂ supports were carefully examined. It was found that there was a preferential orientation relationship between Au nanoparticles and the CeO₂ support. It was also observed that small and thin Au nanoparticles disappeared during TEM observation, shrinking layer by layer down to a mono-atomic layer.     

Chitosan-coated anisotropic silver nanoparticles as a SERS substrate for single-molecule detection

Surface-enhanced Raman spectroscopy (SERS) is a technique that has become widely used for identifying and providing structural information about molecular species in low concentration. There is an ongoing interest in finding optimum particle size, shape and spatial distribution for optimizing the SERS substrates and pushing the sensitivity toward the single-molecule detection limit. This work reports the design of a novel, biocompatible SERS substrate based on small clusters of anisotropic silver nanoparticles embedded in a film of chitosan biopolymer. The SERS efficiency of the biocompatible film is assessed by employing Raman imaging and spectroscopy of adenine, a significant biological molecule. By combining atomic force microscopy with SERS imaging we find that the chitosan matrix enables the formation of small clusters of silver nanoparticles, with junctions and gaps that greatly enhance the Raman intensities of the adsorbed molecules. The study demonstrates that chitosan-coated anisotropic silver nanoparticle clusters are sensitive enough to be implemented as effective plasmonic substrates for SERS detection of nonresonant analytes at the single-molecule level.     

Gold nanoparticles deposited on fluorine-doped tin oxide substrates as materials for laser operated optoelectronic devices

We have discovered occurrence of strong narrow spectral lines in gold nanoparticles deposited on fluorine-doped tin oxide substrates at wavelengths 410, 440 and 550 nm under influence of 808 nm wavelength laser illumination with power about 200 mW. These lines appear just after the 1 s of illumination and are almost unchanged during all the remaining time of illumination. Such lines are absent for the other content of gold nanoparticles-modified substrates. So a principle role here is played by the inter-particle distances. The relaxation process is continued during 8–10 h and the samples return to their initial states. The occurrence of the such narrow spectral lines may be a consequence of the two-photon absorption related with the corresponding electron–phonon interactions due to specific interactions between the plasmons and the phonon subsystem and the free carriers.     

Heterogeneous precipitation of silver nanoparticles on kaolinite plates

Two different methods to obtain silver nanoparticles supported on kaolin crystals have been performed: the first one followed a thermal reduction and the second one a chemical reduction. In both cases, the silver nanoparticles with two different average particles size (ca.12 and 30 nm) were perfectly isolated and attached to the surface of the kaolin plates. The silver nanoparticles were localized mainly at the edge of the single crystal plates, the hydroxyl groups being the main centres of adsorption. The samples were fully characterized by XRD, UV-vis spectroscopy and TEM. The antimicrobial benefits of the composites were evaluated as antibacterial against common Gram-positive and Gram-negative bacteria, and antifungal activity against yeast. The results indicated a high antimicrobial activity for Escherichia coli JM 110 and Micrococcus luteus, while being inactive against yeast under our experimental conditions. The chemical analysis of Ag in the fermentation broths show that only a small portion of metal (<9 ppm) is released from the kaolin/metakaolin particles. Therefore, the risk of toxicity due to a high concentration of metal in the medium is minimized.     

Direct nucleation of silver nanoparticles on graphene sheet

Silver (Ag) nanoparticles were synthesized on the surface of graphene sheet by the simultaneous reduction of Ag+ and graphene oxide (GO) in the presence of simple reducing agent, hydrazine hydrate (N2H4 x H2O). Both the Ag+ and GO were reduced and Ag+ was nucleated onto graphene. GO flakes were prepared by conventional chemical exfoliation method and in the presence of strong acidic medium of potassium chlorate. Silver nanoparticles were prepared using 0.01 M AgNO3 solution. The reduced GO sheet decorated with Ag is referred as G-Ag sample. G-Ag was characterized by FTIR (Fourier transform infrared) spectroscopy using GO as standard. An explicit alkene peak appeared around 1625 cm(-1) was observed in G-Ag sample. Besides, the characteristic carbonyl and hydroxyl peaks shows well reduction of GO. The FTIR therefore confirms the direct interaction of Ag into Graphene. SEM (scanning electron microscopy) and TEM (transmission electron microscopy) analysis were performed for morphological probing. The average size of Ag nanoparticles was confirmed by around 5-10 nm by the high-resolution TEM (HRTEM). The Ag quantum dots incorporated nanocomposite material could become prominent candidate for diverse applications including photovoltaic, catalysis, and biosensors etc.