超支化聚(胺-酯)为模板Ag纳米粒子的制备

以超支化聚(胺-酯)为模板,采用NaBH4直接还原和紫外灯光照射合成了Ag纳米粒子。超支化聚(胺-酯)对Ag纳米粒子形成起着重要的作用。TEM分析表明,Ag纳米粒子形貌为球形结构,分布均匀,粒径约为45 nm(NaBH4还原)和20 nm(紫外灯光照射)。发现在UV-Vis谱图中420 nm左右有Ag纳米粒子特征表面等离子共振吸收峰。FT-IR分析发现Ag纳米粒子和超支化聚(胺-酯)之间有较强的相互作用,超支化聚(胺-酯)对Ag纳米粒子的稳定性起保护作用。     

Kinetic studies on water-soluble gold nanoparticles coordinated to poly(vinylpyrrolidone): isotropic to anisotropic transformation and morphology

The growth kinetics, isotropic-to-anisotropic transformation, structural properties and surface morphology of polyvinylpyrrolidone (PVP)-coordinated gold nanoparticles are reported in this work. The reduction of gold ions, kinetics, and growth mechanism of gold nanoparticles, and the coordination between PVP and gold are explored for the first time in this single report. The layer-by-layer growth mechanism (adsorption of gold ions to the nuclei and their subsequent reduction) was observed in the growth of isotropic nanoparticles during the initial stage of the reaction, whereas the Ostwald ripening mechanism (growth of larger particles at the expense of smaller particles) was observed in the growth of the anisotropic nanoparticles in the later stage of the reaction. The surface plasmon resonance band for the anisotropic nanoparticles (average size for a typical sample was ca. 9 nm) was blue-shifted (20 nm) toward that of the isotropic nanoparticles (whose average size is much smaller than that of the anisotropic nanoparticles). The increased effective electron density on the surface of anisotropic particles was the cause of this blue shift. The resultant gold colloids were very stable because the PVP molecules were coordinated through both the C–N and C=O groups, instead of the C=O group alone. The positions of the surface plasmon band and morphology of the gold products were strongly dependent on the amount of PVP.     

Combined electrochromic and plasmonic optical responses in conducting polymer/metal nanoparticle films

Poly(3,4-ethylenedioxithiophene)/poly(styrene sulphonate) (PEDOT/PSS) aqueous dispersions were mixed with aqueous gold nanoparticle and aqueous silver nanoparticle colloids. PEDOT/gold nanoparticles (Au NP) and PEDOT/silver nanoparticles (Ag NP) films were obtained by solvent casting the corresponding aqueous solutions. The nanocomposite films showed the optical characteristics associated with both the surface plasmon absorption resonance of the metal nanoparticles and the excitation of the bipolaron band of the conducting polymer. As an interesting application we demonstrate the use of metal nanoparticles to tune the color of PEDOT based electrochromic films from blue to violet in the case of Au NP or green in the case of Ag NP.     

Optical organophosphate sensor based upon gold nanoparticle functionalized fumed silica gel

We report on the creation of a high surface area, chemically selective material for the efficient adsorption of organophosphate and organophosphonate species. Using silica microparticles in conjunction with gold nanoparticles and surface modification chemistry, we have demonstrated a material with a binding constant for organophosphonates and organophosphates (OPPs) of K=2x10(6) M-1. The binding of OPPs to the modified gold nanoparticles appears as a spectral shift in the gold nanoparticle resonance. The sensitivity of this technique is limited by scattering losses of suspensions of the particles, and we report on how this sensitivity can be recovered to a significant extent by the use of solvents with a refractive index close to that of the silica particles.     

Green synthesis of highly stabilized nanocrystalline silver particles by a non-pathogenic and agriculturally important fungus T. asperellum

A controlled and up-scalable biosynthetic route to nanocrystalline silver particles with well-defined morphology using cell-free aqueous filtrate of a non-pathogenic and commercially viable biocontrol agent Trichoderma asperellum is being reported for the first time. A transparent solution of the cell-free filtrate of Trichoderma asperellum containing 1?mM AgNO(3) turns progressively dark brown within 5?d of incubation at 25?°C. The kinetics of the reaction was studied using UV-vis spectroscopy. An intense surface plasmon resonance band at ～410?nm in the UV-vis spectrum clearly reveals the formation of silver nanoparticles. The size of the silver particles using TEM and XRD studies is found to be in the range 13-18?nm. These nanoparticles are found to be highly stable and even after prolonged storage for over 6 months they do not show significant aggregation. A plausible mechanism behind the formation of silver nanoparticles and their stabilization via capping has been investigated using FTIR and surface-enhanced resonance Raman spectroscopy.     

Comparative study of Ag and Au nanoparticles biosensors based on surface plasmon resonance phenomenon

The specific sensitivity of surface plasmon resonance to changes in the local environment of nanoparticles allows their use as platforms to probe chemical and biochemical binding events on their surfaces without any labeling [1], [2], [3], [4]. In this paper, we perform a comparative study of gold and silver nanoparticle based biosensors, prepared within the same conditions, in order to determine which metal seems the best for biological sensing. The prototypical biocytin–avidin interaction is used to study gradual changes over time and with avidin concentration in the absorption spectra bands of biocytinylated 10 nm silver and gold nanospheres. First, the Ag nanoparticles plasmon resonance absorbance signal is about 10 times larger than the Au one. Secondly, for an equivalent concentration of avidin, the optical property modifications are more pronounced for silver nanoparticles than for gold ones of the same geometry. These observations attest the superiority of Ag on Au nanoparticles when optical considerations are only taken into account. Finally, with both biosensors, the specificity of the interaction, checked by replacing avidin with bovine serum albumin, is relatively poor and needs to be improved.     

Shape-controlled synthesis of NIR absorbing branched gold nanoparticles and morphology stabilization with alkanethiols

Gold nanoparticles are ideal candidates for clinical applications if their plasmon absorption band is situated in the near infrared region (NIR) of the electromagnetic spectrum. Various parameters, including the nanoparticle shape, strongly influence the position of this absorption band. The aim of this study is to produce stabilized NIR absorbing branched gold nanoparticles with potential for biomedical applications. Hereto, the synthesis procedure for branched gold nanoparticles is optimized varying the different synthesis parameters. By subsequent electroless gold plating the plasmon absorption band is shifted to 747.2 nm. The intrinsic unstable nature of the nanoparticles' morphology can be clearly observed by a spectral shift and limits their use in real applications. However, in this article we show how the stabilization of the branched structure can be successfully achieved by exchanging the initial capping agent for different alkanethiols and disulfides. Furthermore, when using alkanethiols/disulfides with poly(ethylene oxide) units incorporated, an increased stability of the gold nanoparticles is achieved in high salt concentrations up to 1 M and in a cell culture medium. These achievements open a plethora of opportunities for these stabilized branched gold nanoparticles in nanomedicine.     

Enhanced wound healing activity of Ag–ZnO composite NPs in Wistar Albino rats

In the present study, silver (Ag) and Ag–zinc oxide (ZnO) composite nanoparticles (NPs) were synthesised and studied their wound‐healing efficacy on rat model. Ultraviolet–visible spectroscopy of AgNPs displayed an intense surface plasmon (SP) resonance absorption at 450 nm. After the addition of aqueous Zn acetate solution, SP resonance band has shown at 413.2 nm indicating a distinct blue shift of about 37 nm. X‐ray diffraction analysis Ag–ZnO composite NPs displayed existence of two mixed sets of diffraction peaks, i.e. both Ag and ZnO, whereas AgNPs exhibited face‐centred cubic structures of metallic Ag. Scanning electron microscope (EM) and transmission EM analyses of Ag–ZnO composite NPs revealed the morphology to be monodispersed hexagonal and quasi‐hexagonal NPs with distribution of particle size of 20–40 nm. Furthermore, the authors investigated the wound‐healing properties of Ag–ZnO composite NPs in an animal model and found that rapid healing within 10 days when compared with pure AgNPs and standard drug dermazin.Inspec keywords: wounds, tissue engineering, biomedical materials, nanocomposites, nanofabrication, nanomedicine, silver, zinc compounds, II‐VI semiconductors, wide band gap semiconductors, ultraviolet spectra, visible spectra, nanoparticles, particle size, surface plasmon resonance, spectral line shift, X‐ray diffraction, scanning electron microscopy, transmission electron microscopyOther keywords: enhanced wound healing activity, Ag‐ZnO composite nanoparticles, Wistar Albino rats, wound‐healing efficacy, ultraviolet‐visible spectroscopy, intense surface plasmon resonance absorption, aqueous Zn acetate solution, SP resonance band, blue shift, X‐ray diffraction analysis, diffraction peaks, face‐centred cubic structures, scanning electron microscope, SEM, transmission electron microscope, TEM, monodispersed hexagonal nanoparticles, quasihexagonal nanoparticles, particle size, animal model, time 10 d, size 20 nm to 40 nm, Ag‐ZnO     

Characterization of gold nanoparticles in organic or inorganic medium (ethanol/water) fabricated by spark discharge method

In this paper a method of spark discharge method (SDM) for producing gold nanoparticles in organic or inorganic medium (pure ethanol/deionized water) is proposed. The microstructure of SDM-produced gold nanoparticles was examined by Transmission Electron Microscopy. The crystal structure and surface plasmon resonance of the nanoscale gold particles were studied using X-ray diffraction and UV-Visible spectroscopy. Zeta potential analysis showed that negative charges on the particle surface may be contributing to the stability of the suspension. The experiment's results revealed that SDM is an alternative process to synthesize gold nanoparticle suspension with different particle sizes and shapes in different media without any surfactant.     

Effect of solvent refractive index on the surface plasmon resonance nanoparticle optical absorption

Optical properties of plasmon coupled silver and gold nanoparticles were studied as a function of the refractive index of the surrounding medium. Our studies confirmed that the effect of changes in the refractive index of the surrounding medium was more difficult to demonstrate from an experimental point of view, because of the very high susceptibility of nanoparticles to aggregate in aqueous and organic solvents. Whereas the position of the absorption bands of triiodide in these solvents shows a clear dependence on medium's refractive index, the surface plasmon band position of silver and gold nanoparticles do not exhibit the same dependence. This is attributed to a non-negligible interaction of these solvents with nanoparticle surfaces.     

Characterisation,Luminescence and Antibacterial Properties of Stable AgNPs Synthesised from AgCl by Precipitation Method

Silver nanoparticles(AgNPs) were synthesised using equimolar concentrations of reducing agent vitamin C and AgCl precursor by simple precipitation method. The synthesised AgNPs were characterised by X-ray diffraction(XRD), UV-Visible, photoluminescence and field emission scanning electron microscopy(FESEM)analysis. The formation of AgNPs was confirmed by the typical surface plasmon resonance band at 426 nm.The presence of elemental silver and pure crystalline face centre cubic(fcc) structure was confirmed by energy dispersive X-ray analysis and XRD analysis, respectively. The FESEM images showed the formation of spherical AgNPs for lower concentrations(0.1 and 0.3 mol/L) while spike and flower shaped particles were formed for higher concentration. Photoluminescence characteristic band was observed with no shift at 390 nm indicating the stable nature of AgNPs. The antibacterial property of the AgNPs was tested against gram negative bacteria Pseudomonas aeruginosa by using Cissus quadrangular as a control and the result showed that vitamin C reduced AgNPs have good antibacterial activity.     

Effect of pH on the extra cellular synthesis of gold and silver nanoparticles by Saccharomyces cerevisae

In the present study, the synthesis of gold and silver nanoparticles was investigated using the culture supernatant broth of the yeast Saccharomyces cerevisae. Gold nanoparticles were formed within 24 hours of gold ion coming in contact with the culture supernatant broth. In case of silver the reduction process took 48 hours. The synthesized nanoparticles were investigated by UV-Visible spectroscopy. Distinct surface plasmon peaks were observed at 540 nm and 415 nm for gold and silver nanoparticles respectively. Bio-TEM micrographs of the synthesized nanoparticles indicated that the particles were well dispersed and near spherical in shape. The size range of the gold and silver nanoparticles was around 20-100 nm and 5-20 nm respectively. XRD patterns showed the presence of three distinct peaks corresponding to gold and silver nanoparticles respectively. A pH range of 4 to 6 and 8 to 10 favored optimum synthesis of gold and silver nanoparticles respectively. The process of reduction being extra cellular could be used in future for downstream processing in an eco friendly manner.     

Silver nanoparticle-oligonucleotide conjugates based on DNA with triple cyclic disulfide moieties

We report a new strategy for preparing silver nanoparticle-oligonucleotide conjugates that are based upon DNA with cyclic disulfide-anchoring groups. These particles are extremely stable and can withstand NaCl concentrations up to 1.0 M. When silver nanoparticles functionalized with complementary sequences are combined, they assemble to form DNA-linked nanoparticle networks. This assembly process is reversible with heating and is associated with a red shifting of the particle surface plasmon resonance and a concomitant color change from yellow to pale red. Analogous to the oligonucleotide-functionalized gold nanoparticles, these particles also exhibit highly cooperative binding properties with extremely sharp melting transitions. This work is an important step toward using silver nanoparticle-oligonucleotide conjugates for a variety of purposes, including molecular diagnostic labels, synthons in programmable materials synthesis approaches, and functional components for nanoelectronic and plasmonic devices.     

Luminescence of CdSe quantum dots near a layer of silver nanoparticles ion-synthesized in sapphire

We study the characteristics of the luminescence of composite films based on polymethyl methacrylate with CdSe quantum dots deposited from solution onto the surface of a sapphire substrate containing a preliminarily formed layer with ion-synthesized silver nanoparticles. The sapphire layer with silver nanoparticles exhibits selective plasmon absorption in the visible spectral range with a peak at 463 nm. Enhancement in the exciton luminescence intensity of quantum dots with a peak at 590 nm is observed upon excitation at wavelengths lying in the region of plasmon resonance of metal nanoparticles, as well as luminescence quenching for quantum dots located in the vicinity of silver nanoparticles.     

Distance-dependent plasmon resonant coupling between a gold nanoparticle and gold film

We present an experimental analysis of the plasmonic scattering properties of gold nanoparticles controllably placed nanometers away from a gold metal film. We show that the spectral response of this system results from the interplay between the localized plasmon resonance of the nanoparticle and the surface plasmon polaritons of the gold film, as previously predicted by theoretical studies. In addition, we report that the metal film induces a polarization to the single nanoparticle light scattering, resulting in a doughnut-shaped point spread function when imaged in the far-field. Both the spectral response and the polarization effects are highly sensitive to the nanoparticle-film separation distance. Such a system shows promise in potential biometrology and diagnostic devices.     

Influence of the interaction between two Ag nanoparticles on optical properties of Ag/PGMEA nanocomposite materials

We report local electric field calculations in Ag/PGMEA nanocomposite materials using the dipole discrete approximation. We employ calculation and simulation to show that the nanoparticle radius and the interparticle distance could control and tune the surface plasmon resonances, which influence the extinction spectra and the near-field enhancement of Ag/PGMEA nanostructures. With decreasing interparticle distance, the near-field coupling between particles will induce the shift of surface plasmon resonance peak and improve the near-field intensity. With increasing radius (r), the resonance wavelength peak is red-shifted because of the interaction between two Ag nanoparticles. At 449 nm, the highest near-field enhancement factor obtained in the center of the gap was 30.5 for two interacting Ag nanoparticles of r = 11 nm with a gap of 5 nm.     

Real-time, in-situ, extinction spectroscopy studies on silver-nanoseed formation

In this paper, real-time extinction spectroscopy was employed to analyze in situ the fast formation process of silver seeds. The influencing factors for silver-seed formation, including the concentration of the reducer (NaBH(4)), the amount of stabilizer (citrate), and the addition procedure of NaBH(4), were evaluated. The configuration of the surface plasmon resonance (SPR) spectra of silver nanoparticles, which reflected the morphology of the produced silver seeds, was found to be distinctly affected by the NaBH(4) concentration. Homogeneous silver nanoparticles were obtained when the added NaBH(4) was lower in concentration than 2.00 mM. In contrast, higher concentrations of reducing agent (≥3.00 mM NaBH(4)) resulted in uneven silver nanoparticles. Mie theory was applied to clarify the correlation of the SPR and the size of the silver seeds. Repeated additions of a small amount of the reducing agent could increase the monodispersity and isotropy of silver seeds. Real-time extinction spectroscopy is a convenient technique that achieves the in-situ and nondestructive measurement of intermediates in the formation process of silver nanoseeds.     

Bio-synthesis of gold nanoparticles by human epithelial cells, in vivo

Healthy epithelial cells, in vivo, have the ability to synthesize gold nanoparticles when aqueous tetrachloroauric acid is made to react with human skin. Neither a reducing agent nor a protecting chemical is needed for this bio-synthesis method. The first indication of gold nanoparticle formation is the staining of the skin, which turns deep purple. Stereoscopic optical micrographs of human skin tissue in contact with aqueous tetrachloroauric acid clearly show the staining of the epithelial cells. The UV-Vis spectrum of these epithelial cells shows an absorption band with a maximum at 553 nm. This absorption peak is within the wavelength region where the surface plasmon resonance (SPR) band of aqueous colloidal gold exhibits a maximum. Transmission electron micrographs show that gold nanoparticles synthesized by epithelial cells have sizes between 1 and 100 nm. The electron diffraction pattern of these nanoparticles reveals a crystalline structure whose interplanar distances correspond to fcc metallic gold. Transmission electron micrographs of ultra-thin (70 nm thick) slices of epithelial cells clearly and undoubtedly demonstrate that gold nanoparticles are inside the cell. According to high resolution transmission electron micrographs of intracellular single gold nanoparticles, they have the shape of a polyhedron.     

Annealing of polymer films with embedded silver nanoparticles: Effect on optical properties

The influence of annealing time and of the silver over polymer ratio on the optical properties of the silver nanoparticles embedded in a poly(vinyl alcohol) matrix has been analyzed by spectroscopic ellipsometry in the visible/near-infrared spectral domains. The complex refractive index shows a localized absorption near 420 nm which can be attributed to localized surface plasmons. An atomic force microscopy topographic analysis shows that the particles were nearly spherical with an average size less than 20 nm, as confirmed by optical transmission measurements with polarized light. The size of the particles and their number respectively decreased and increased as the annealing time of the film increased, yielding a plasmon absorption band whose intensity is correlated to the silver nanoparticles density, estimated from their nearest-neighbour distance.     

Synthesis and characterization of titania-coated silver nanoparticles

Silver particles of 70 +/- 10 nm mean diameter were coated with uniform layers of amorphous titania by the hydrolysis and polycondensation process using titanium(IV) n-butoxide in aqueous solution. Because of the large dielectric function of titania, a shift to the longer wavelengths was observed for the plasmon resonance maximum of coated silver nanoparticles. By changing the alkoxide to particles ratio in the reaction mixture, thickness ranging from 5 to 20 nm was obtained. Hydrothermal treatment performed on coated particles at 350 degrees C for 4 h converted amorphous titania to the anatase crystalline form. The anatase form was confirmed by X-ray powder diffraction. More red shift of the plasmon resonance was observed for the hydrothermally treated samples compared with the particles coated with amorphous titania.