Negative differential resistance and improved optoelectronic properties in Ag nanoparticles-decorated graphene oxide–riboflavin hybrids

Silver nanoparticles (Ag NPs) are decorated on graphene oxide (GO)–riboflavin (R) hybrids produced with three different compositions. The SEM micrographs of the GO–R–Ag materials show a helical fibrillar morphology different from the bar and wrinkled sheet morphology of R and GO, respectively. FT-IR spectra indicate that GO produces a supra molecular complex with R and Ag NPs are stabilized by both R and GO. The UV–vis spectra show a large shift of surface plasmon band from 390 to 570 nm and the circular dichroism spectra indicate a drastic change in the GO–R–Ag system over the GO–R system for a weight ratio of GO to R of 13, suggesting that Ag NPs are wrapped by both the GO–R hybrid and R moieties. The PL-intensity of R increases in the GO–R hybrids but it decreases in the GO–R–Ag ones. The dc-conductivity of the GO–R hybrids increases by 2–3 orders of magnitude on addition of Ag NPs. The I–V characteristic curves of the GO–R–Ag (GO/R = 1/3) material shows a negative differential resistance. Possible reasons from the charge trapping on the Ag NPs followed by stabilization by R are discussed and a model using the density of states approach is proposed.     

Synergistic antimicrobial effects of polyaniline combined with silver nanoparticles

Silver/polyaniline nanocomposites (Ag NPs/PANI) containing PANI nanofiber and Ag nanoparticles were synthesized by one-step approach without using any extra reducing agent or surfactant and applied to new antimicrobial agents. Morphologies and crystallinity of the nanocomposites were characterized with SEM and XRD. The results showed that the average diameter of the PANI nanofibers is around 50–150 nm, and the average particle size of Ag NPs is around 100 nm. The crystallinity of PANI gets better with increasing silver nitride concentration. UV–vis absorption spectroscopy analysis indicated that the Ag NPs have some effect on the microstructure of PANI. The antimicrobial properties of Ag NPs/PANI against Gram-negative Escherichia coli, Gram-positive Staphylococcus aureus and fungous Yeast were evaluated using viable cell counts. The test results demonstrated that Ag NPs/PANI have enhanced antimicrobial efficacy compared to that of pure Ag NPs or pure PANI under the same test condition. The mechanism of the synergistic antimicrobial effect of Ag NPs with PANI was also proposed. In addition, thermal gravity analysis indicated that pure PANI and Ag NPs/PANI exhibit better thermal stability. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Photocrosslinkable acid urethane dimethacrylates from renewable natural oil and their use in the design of silver/gold polymeric nanocomposites

Castor oil-based acid urethane macromers were prepared and employed for obtaining Ag/Au/polymer nanocomposites. Structure and UV induced photopolymerization of the macromers were investigated by spectral methods. The polymerization rate and the degree of conversion decreased with about 10% in the presence of 2.5 wt.% silver nanoparticles (Ag NPs). For the diacid macromer, the surface plasmon intensity increased with irradiation time (the optical density of the absorption maximum (430 nm) attained 2.3 after 600 s), whereas a diminished efficiency was found for Ag NPs in situ generated. Transmission electron microscopy and X-ray photoelectron spectroscopy confirmed uniform distribution of the spherical nanoparticles (0.6 nm (Ag NPs); 5 nm (Au NPs)) and the appearance of Ag 3d_3/2, Ag 3d_5/2, Au 4f_7/2 and Au 4f_5/2 peaks corresponding to Ag (0) or Au (0). Environmental scanning electron microscope with energy-dispersive X-ray detector, contact angle and mechanical parameters measurements complemented the above observations.     

Adsorption of Silver Nanoparticles onto Different Surface Structures of Chitin/Chitosan and Correlations with Antimicrobial Activities

Size-controlled spherical silver nanoparticles (Ag NPs) can be simply prepared by autoclaving mixtures of glass powder containing silver with glucose. Moreover, chitins with varying degrees of deacetylation (DDAc < 30%) and chitosan powders and sheets (DDAc > 75%) with varying surface structure properties have been evaluated as Ag NP carriers. Chitin/chitosan-Ag NP composites in powder or sheet form were prepared by mixing Ag NP suspensions with each of the chitin/chitosan-based material at pH 7.3, leading to homogenous dispersion and stable adsorption of Ag NPs onto chitin carriers with nanoscale fiber-like surface structures, and chitosan carriers with nanoscale porous surface structures. Although these chitins exhibited mild antiviral, bactericidal, and antifungal activities, chitin powders with flat/smooth film-like surface structures had limited antimicrobial activities and Ag NP adsorption. The antimicrobial activities of chitin/chitosan-Ag NP composites increased with increasing amounts of adsorbed Ag NPs, suggesting that the surface structures of chitin/chitosan carriers strongly influence adsorption of Ag NPs and antimicrobial activities. These observations indicate that chitin/chitosan-Ag NPs with nanoscale surface structures have potential as antimicrobial biomaterials and anti-infectious wound dressings.     

Study of antibacterial properties of polypropylene filled with surfactant‐coated silver nanoparticles

Medical applications require, in most cases, antibacterial protection. The use of silver (Ag) gives important antibacterial properties since silver is highly toxic for bacteria. In this research work, we have used silver nanoparticles (Ag NPs) with different surfactants, polyvinyl pyrrolidone (PVP) and oleic acid (OA) to facilitate dispersion. PP‐Ag NPs compounds were prepared by melt mixing, and the effects of the processing conditions on nanoparticles' dispersion were investigated by transmission electron microscopy (TEM). The antibacterial efficiency of PP‐Ag NPs compounds against Staphylococcus aureus ATCC 6538 and Escherichia coli ATCC 8379 was evaluated. Results show that good dispersion is obtained with rotating speeds in the 350–500 rpm range. TEM analysis reveals balanced dispersion and presence of some Ag NPs aggregates. Regarding antimicrobial properties, the use of PVP as surfactant leads to “significant” antimicrobial activity of 1.5 against Staphylococcus aureus and Escherichia coli; on other hand, the use of oleic acid (OA) as surfactant leads to strong protection against Staphylococcus aureus (antimicrobial activity between 2.5 and 3.3) but the overall protection against Escherichia coli is very low (lower than 1). Results show that the use of surfactants for Ag NPs has important effects on antibacterial properties of polypropylene filled with coated Ag NPs. POLYM. ENG. SCI., 2011. © 2011 Society of Plastics Engineers     

Studies on the effect of long-chain and head groups of nonionic surfactants synthesized from palm and coconut oil on the formation of silver nanoparticles

Four fatty amides were synthesized using coconut and palm oil sources. The chemical structure of the as-prepared fatty acids was confirmed using Fourier Transform Infrared (FT-IR) and ¹H, ¹³C NMR spectroscopy. The effect of different chain lengths and head groups of these compounds on Ag nanoparticles (NPs) synthesis was investigated. Ultraviolet–visible spectroscopic studies showed characteristic absorbance peaks (λ_max ≈ 410 nm). FT-IR results indicated that the surfactant functionalities are responsible for the Ag NPs stability. The effect of fatty amides on the morphology and size distribution of the Ag NPs was investigated using transmission electron microscope (TEM). The TEM micrographs showed the formation of fine spherical morphology due to surfactant-mediated self-assembly with an average particle size of 1–3 nm. Dynamic light scattering (DLS) analysis showed the micellar self-assembly of Ag NPs-fatty amides. The effect of surfactant on the solution behavior was analyzed using surface tension measurements. Cocamide and palm DEA showed relatively low free energy (∆G_mic) values, resulting in smaller particles with good distribution. Finally, the Ag NPs showed outstanding antimicrobial activity against Pseudomonas putida bacteria.     

Characterization of molecular interaionic and intraionic crosslinkable sulfonated poly(ether ether ketone‐alt‐benzimidazole) membrane

Lysozyme-loaded polymeric composite microparticles were successfully coprecipitated by solution-enhanced dispersion by supercritical CO₂ (SEDS), starting with a homogeneous organic solvent solution of lysozyme/poly(L -lactide)/poly(ethylene glycol) (lysozyme/PLLA/PEG). The effects of different drug loads (5, 8, and 12% w/w), PLLA Mw (10, 50, 100, and 200 kDa), PEG contents (0, 10, 30, and 50% PEG/(PLLA+PEG) w/w), and PEG Mw (400, 1000, and 4000 kDa) on the surface morphology, particle size, and drug release profile of the resulting composite microparticles were investigated. The results indicate that the size of the microparticles decreased and the rate of drug release increased with an increase in drug load, PEG content, or PEG Mw; the particle size first increased and then decreased with an increase in PLLA Mw, and the drug release was controlled by both particle size and PLLA Mw. The Fourier transform infrared spectrometer analysis and circular dichroism spectra measurement reveal that no significant changes occurred in the molecular structures during the SEDS processing, which is favorable to the production of protein–polymer composite microparticles for a protein drug delivery system. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Tannic acid coating and in situ deposition of silver nanoparticles to improve the antifouling properties of an ultrafiltration membrane

The construction of antifouling membranes has been a desirable approach for addressing membrane-fouling issues in the ultrafiltration (UF) process. Antifouling means antiadhesive and antimicrobial; however, few researchers have achieved both properties in a facile and effective manner. In this article, we report a direct tannic acid (TA) coating method combined with the in situ deposition of silver nanoparticles (Ag NPs); this was used to improve the antifouling properties of a positively charged polymeric UF membrane. The results show that the TA–Ag NP modified membranes showed improved protein resistance (flux recovery rate = 71.2% after modification vs 17.8% before modification) and less attachment of bacteria (Escherichia coli K1) on the membrane surface and reduced cell viability in the resulting bacterial suspension (reduced by ≥90%) because of the combined antimicrobial properties of both the TA and Ag NPs. This indicated that our modification method was promising for UF membrane antifouling applications. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47314.     

Preparation and characterization of SiO2/polydopamine/Ag nanocomposites with long-term antibacterial activity

Silver nanoparticles (Ag NPs) with diameter of approximately 10 nm were prepared by the reduction of silver nitrate using green synthesis, an eco-friendly approach. The synthesized Ag NPs were homogeneously deposited on silicon dioxide (SiO₂) particles modified with dopamine, leading to the formation of SiO₂/polydopamine (PD)/Ag nanocomposites (NCs) with a core–shell–satellite structure investigated by transmission electron microscopy. The Ag content of SiO₂/PD/Ag NCs determined by inductively coupled plasma optical emission spectrometry was approximately 5.92 wt%. The antibacterial properties of both Ag NPs and SiO₂/PD/Ag NCs against Vibrio natriegens (V. natriegens) and Erythrobacter pelagi sp. nov. (E. pelagi) were investigated by bacterial growth curves and inhibition zone. Compared to Ag NPs, the SiO₂/PD/Ag NCs exhibited superior long-term antibacterial activity, attributed to its controlled release of Ag⁺ ions.     

Synthesis of Bimetallic Nanoparticles (Au–Ag Alloy) Using <Emphasis Type="Italic">Commelina nudiflora L.</Emphasis> Plant Extract and Study its on Oral Pathogenic Bacteria

In present study, biosynthesis of Au–Ag alloy nanoparticles (NPs) using Commelina nudiflora aqueous extract as a stabilizing and reducing agent is reported. The crystalline nature, size, shape and composition of synthesized Au–Ag alloy NPs were characterized by UV–Vis spectrophotometer, field emission scanning electron spectroscopy, energy dispersive X-ray spectroscopy, transmission electron microscope, X-ray diffraction and fourier transform-infrared spectroscopy (FT-IR). The synthesized Au–Ag alloy NPs exhibited different ranges of sizes between 20 and 80 nm with different morphology such as spherical, rod and triangular. FT-IR spectral data revealed that the plant extract contains amine, alcohol, phenol and alkane molecules which are critically involved in the formation of Au–Ag alloy NPs. Finally, the biosynthesized Au–Ag alloys NPs exhibited a strong minimum inhibitory, minimum bactericidal activity against selected oral pathogenic bacteria. The present study gives an important suggestion on plant extract mediated synthesis bimetallic NPs (Au–Ag alloy) emphasis on oral pathogenic bacteria activities.     

Enhanced sensitivity of a direct SERS technique for Hg(2+) detection based on the investigation of the interaction between silver nanoparticles and mercury ions

Mercury which is a very important pollutant has drawn significant attention in recent research. So far, among the various detection methods, the strategies based on surface-enhanced Raman scattering (SERS) are quite attractive because of the high sensitivity, and especially as it is reported that Hg(2+) can be directly detected by SERS without tagging. However, the procedure for the direct SERS detection of mercury is still unclear with little experimental evidence, limiting further development of Hg(2+) detection by SERS. Herein, we performed a simple method based on SERS for the detection of mercury ions in water without tagging. It is established that in only 2 min, low concentration of Hg(2+) can be recognized based on the decrease of SERS intensity. The detection procedure is investigated by multiple characterizations and the mechanism proven by the obtained data provides a practical way to further improve the sensitivity of the SERS detection. It is demonstrated that the interaction between Hg(2+) and Ag nanoparticles (Ag NPs) could occur in a short time, which includes the complexation of Hg(2+) with citrate and the formation of amalgam due to the reduction of Hg(2+). This interaction influences the surface plasmon resonance (SPR) property of Ag NPs and thereby decays the electromagnetic enhancement of Ag NPs; meanwhile the interaction also causes the zeta potential decrease of Ag NPs and accordingly affects the adsorption of Raman reporter molecules on the surface of Ag NPs. Therefore, the weakness of SERS intensity in the presence of Hg(2+) should be mainly attributed to the interaction between Hg(2+) and Ag NPs. From the mechanism demonstrated, it can be speculated that using fewer Ag NPs in the detection could improve the sensitivity, because at low Hg(2+) concentration the interaction becomes stronger since every Ag nanoparticle acts with more Hg(2+) ions. Accordingly, we establish that 90.9 pM (18.2 ppt) Hg(2+) is detected in 18 μM Ag NPs, which is much lower than that in reported papers.     

Green Chemical Synthesis of Silver Nanoparticles and its Catalytic Activity

Silver nanoparticles (Ag(0) NPs) were synthesized by the chemical reduction method, in which ceftriaxone (antibiotic) used as reducing (to convert Ag⁺ to Ag(0)) and capping agent. UV–Visible spectroscopy revealed the first indication of formation of Ag(0) NPs. FT-IR spectroscopy showed the interaction of formation of bonding between antibiotic standard and silver. X-ray powder diffraction powder pattern confirmed the crystalline nature of prepared Ag(0) NPs. These Ag(0) NPs were used as catalyst for three organic hazardous chemicals i.e., 4-nitro-1,3-Phenylene diamine, 6-methyl-2-nitroanilline, 4-methyle-2-nitroanilline. The prepared Ag(0) NPs showed good catalytic activity against these compounds.     

Cefditorene-Mediated Synthesis of Silver Nanoparticles and Its Catalytic Activity

Ag(0) NPs were prepared by chemical reduction method in which silver nitrate was taken as the metal precursor and cefditorene as a reducing/capping agent and NaOH as the catalyst for reaction enhancement. The formation of the Ag(0) NPs was monitored using UV–Vis absorption spectroscopy confirmed the formation of Ag(0) NPs by exciting the typical surface plasmon absorption maxima at 405 nm. Transmission electron microscopy (TEM) confirmed the spherical morphology of the (Ag(0) NPs). The crystallite (11 ± 3 nm) and particle size (14.1 ± 2.2 nm) obtained from TEM and XRD analysis were coinciding with each other. Prepared Ag(0) NPs were then used as catalyst against 2-nitroaniline, 3-nitroaniline and 4-nitroaniline, which all showed best catalytic activity.     

Antimicrobial properties of silver nanoparticles synthesized by bioaffinity adsorption coupled with TiO2 photocatalysis

BACKGROUND: On the basis of effective bioaffinity adsorption of Ag⁺, silver nanoparticles (Ag NPs) were synthesized on the surface of chitosan‐TiO₂ adsorbent (CTA) by TiO₂ photocatalysis for crystal growth. RESULTS: Among the microstructure characterizations of the resulting silver nanoparticles‐ loaded chitosan‐TiO₂ adsorbent (Ag‐CTA), X‐ray diffraction (XRD) and scanning electron microscopy (SEM) equipped with energy dispersive X‐ray (EDX) revealed the formation of metallic Ag on the CTA, which was further confirmed by the surface plasmon resonance of Ag NPs in the UV‐visible absorption spectrum. The underlying mechanism behind the formation of Ag NPs on the CTA by TiO₂ photoreduction was studied by Fourier transform infrared (FTIR) spectroscopy. The distinctive feature of Ag‐CTA after adsorption was the highly efficient antimicrobial activity in inactivating different test strains. In the case of Escherichia coli, 1.50 mg 1.67 wt% Ag‐CTA could totally inhibit 1.0–1.2 × 10⁷ colony forming units (CFU) in 100 mL nutrient medium, which was superior to that previously reported. CONCLUSIONS: CTA effectively adsorbed the precious metal ion Ag⁺ onto active imprinting sites on the adsorbent and then exerted efficient antimicrobial effects against diverse microbes. This research will be useful for designing a novel CTA‐based wastewater treatment for multi‐functional performance. Copyright © 2010 Society of Chemical Industry     

A promising technique of Aegle marmelos leaf extract mediated self‐assembly for silver nanoprism formation

The Aegle marmelos leaf extract (LE) mediated synthesis of prismatic and spherical Ag nanoparticles (NPs) has been studied. The formation of prismatic structures from spherical NPs was observed microscopically using scanning electron microscope, transmission electron microscope, and atomic force microscope. The shape transformation from spherical NPs to prismatic nanostructures was studied by simply changing LE concentration, keeping constant AgNO₃ concentration (1 mM). The role of pH toward prism formation and the effect of sonication on the formed structures were also investigated. The antimicrobial activity of the synthesized Ag spherical/prismatic NPs was evaluated against gram negative bacteria (Escherichia coli, Pseudomonas aeruginosa) and on a phytopathogen Fusarium solani. This green synthesis approach for the synthesis of prismatic Ag nanostructures may be useful for surface‐enhanced Raman spectroscopy application for the detection of low concentration organic molecules, apart from the studied antimicrobial activity. © 2017 American Institute of Chemical Engineers AIChE J, 63: 3670–3680, 2017     

Enhanced the dispersibility and permeability of silver nanoparticles over rGO grafted by positively-charged polyethyleneimine toward broad-spectrum sterilization

Silver nanoparticles (Ag NPs) are used as antimicrobial agents due to their high-efficiency, broad-spectrum disinfection activity. However, the agglomeration and stability problems caused by excessive release of silver ions (Ag⁺) have severely restricted their developments. Herein, a novel silver/polyethyleneimine/reduced graphene oxide (Ag/PEI/rGO) antibacterial material featuring good dispersibility and permeability was rationally designed, thus benefiting for the capture of bacteria due to the introducing of highly-cationic PEI modifier and controllable release of biocidal agents (Ag⁺). Compared with Ag/rGO, the Ag/PEI/rGO has excellent stability and shows a more efficient sterilization efficacy against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) with 100% germicidal efficiency with low orders of dozens of ppm. In addition, the outstanding biocompatibility of this Ag/PEI/rGO antibacterial material endows it with promising potential in sterilization applications, which is expected to solve the infection problem caused by bacterial biofilm formation.     

Poly(dimethylsiloxane)‐containing thermoplastic elastomer/gold–silver alloy nanocomposites for thermally/oxidatively stable and antimicrobial coating

Polymer materials with embedded silver (Ag) nanoparticle (NP) are of considerable interest owing to their enhanced antimicrobial activity and physical properties compared to host polymer. Antimicrobial and thermally/oxidatively stable coating not only enhances the durability of the coated material but also reduces the growth of bacteria/fungus and thus reduces the chance of infection. For this purpose, we have prepared polydimethylsiloxane‐containing predominantly poly(meth)acrylates‐based pentablock thermoplastic elastomer (TPE)/gold (Au)–Ag alloy nanocomposites (NCs) with antimicrobial activity and enhanced physical properties. In situ simultaneous reduction of appropriate amount of metal salts in the presence of block copolymer produced Au–Ag NPs of size 5–10 nm. Such embedded 5–10 nm sized particles (loading, 0.1–0.2 wt%) improved the mechanical property, thermal/oxidative stability, and antimicrobial activity of the NCs. The NC films also exhibited tunable surface wetting behavior and optical properties. The NC films showed low level of Ag leaching as confirmed by inductively coupled plasma spectrometer and UV–visible spectroscopy. Improved thermal/oxidative resistance of the TPE/Au–Ag alloy NCs enhanced antimicrobial activity, together with low level of leaching characteristic of the embedded NPs deemed suitable for further use of these NCs material for antimicrobial and oxidatively stable coating applications. POLYM. COMPOS., 36:2103–2112, 2015. © 2014 Society of Plastics Engineer     

Silver-doped titanium dioxide nanoparticles encapsulated in chitosan–PVA film for synergistic antimicrobial activity

The objective of the present study performed was to develop and characterize of silver (Ag)-doped titanium dioxide (TiO₂) naoparticles (NPs) encapsulated in chitosan–polyvinyl alcohol (PVA) film for synergistic antimicrobial activity. The acidic solution of chitosan with PVA was used for the reduction of silver ions into silver NPs using their functional groups such as hydroxyl, carboxyl, and amino groups. The chitosan–PVA silver nanoparticle films showed significant antimicrobial and antifungal activity against Staphylococcus aureus, Candida albicans, and Pseudomonas aeruginosa. Therefore, the present study is an alternative for conventional treatment as antimicrobial film showed synergistic, noninvasive, and economic effects.     

Deposition of silver nanoparticles on single wall carbon nanotubes via a self assembled block copolymer micelles

We demonstrate a facile route to decorate the surface of networked single walled carbon nanotubes (SWNTs) with silver nanoparticles (Ag NPs). The method is based on utilization of either spherical poly(styrene-b-4vinylpyridine) (PS-b-P4VP) or cylindrical poly(styrene-b-acrylic acid) (PS-b-PAA) copolymer micelles capable of stabilizing nanotubes in solution and subsequently forming a thin and uniform block copolymer/SWNTs composite film upon spin coating. The selective doping of silver acetate into either P4VP or PAA domains in a thin composite film, followed by thermal treatment, results in the formation of Ag NPs in the cores of micelles. Further heat treatment at 500 °C sufficiently high for degrading both block copolymers allows us to fabricate a thin SWNTs network in which Ag NPs are efficiently deposited on the surface of nanotubes. A sharp surface plasmon absorption band around 400 nm of the networked SWNTs with Ag NPs confirms the presence of Ag NPs with narrow distribution in their size.     

Synthesis,properties and self‐assembly of intelligent core‐shell nanoparticles based on chitosan with different molecular weight and N‐isopropylacrylamide

In this study, a series of chitosan‐graft‐poly(N‐isopropylacrylamide) (CTS‐g‐PNIPAAm) copolymers based on different molecular weight (Mw) of CTS and NIPAAm were synthesized through the polymerization of NIPAAm in an acid aqueous solution. The structures were verified by Fourier transform infrared and nuclear magnetic resonance. The influence of the CTS Mw on the properties of the resulting copolymers and self‐assembled nanoparticles was fully examined. The grafting ratio and grafting efficiency of the copolymers increased with the CTS Mw. All the copolymers have a similar low critical solution temperature of 33.5°C, which was independent of the CTS Mw. Furthermore, the copolymers were less temperature sensitive, when CTS Mw increased to 200 kDa. Besides, once the CTS Mw increased to 700 kDa, the copolymers were less pH sensitive near the tumor site (from pH 7.4 to 6.8). The copolymers could form uniform nanoparticles once the temperature increased to 34°C, which was reversible. After crosslinking by N,N‐methylenebisacrylamide (MBA), structurally stable nanoparticles could be obtained. The results from Transmission electron microscope (TEM) and Atomic force microscopy (AFM) showed that the MBA crosslinked nanoparticles were uniformly spherical with a loose structure. Surface tension method indicated that the critical aggregate concentrations were 0.045, 0.042, 0.037, and 0.036 mg mL^?1 prepared from CTS 50, 100, 200, and 700 kDa, respectively. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013