Remarks on the reactions of a tetracarboxylic porphyrin with gold and silver ions: A spectrophotometric,TEM and SEM study

The coproporphyrin-I (CPI) behaves as a reducing agent for silver and gold metal ions and as stabilizing agent for the formed colloidal metallic nanoparticles. The peculiarity of silver and gold nanoparticles obtained in the reactions of monomeric form of CPI with their metal ions has been studied. The optical properties of the colloidal forms of these metals have been investigated by UV–Vis spectrophotometry, and their morphology by TEM and SEM measurements. The structures and the size distributions of Ag and Au particles have been characterized and determined by computerized TEM images.     

Fabrication, Characterization, and Surface-Enhanced Raman Activity Study of Silver Coated Gold Nanoparticulate Films

This paper reports a study on the preparation of Ag-clad Au colloidal monolayer films by a combination of colloid self-assembly and liquid phase microwave high-pressure technique. Firstly, monodisperse Au nanoparticles prepared by microwave heating method were assembled onto a quartz slide. Then, these Au colloidal particles on the quartz surface acted as seeds for growing the Ag-clad Au composite particulate films. The obtained particulate films were characterized by UV-Vis spectra and atomic force microscopy. It was found that the thickness of the shell and thus the size of particles in the composite colloidal films could be controlled by deposition of Ag on the preformed Au colloidal particle film in the microwave reaction system, and such films significantly increased the surface-enhanced Raman scattering enhancement （SERS） ability compared with Au colloidal particle films. Their strong enhancement ability may mainly stem from relatively large particle consisting of Ag cladding as well as effective coupling among particles in the Ag-clad Au particle ftlms.     

Dielectric response of a concentrated colloidal suspension in a salt-free medium

In this paper the complex dielectric constant of a concentrated colloidal suspension in a salt-free medium is theoretically evaluated using a cell model approximation. To our knowledge this is the first cell model in the literature addressing the dielectric response of a salt-free concentrated suspension. For this reason, we extensively study the influence of all the parameters relevant for such a dielectric response: the particle surface charge, radius, and volume fraction, the counterion properties, and the frequency of the applied electric field (subgigahertz range). Our results display the so-called counterion condensation effect for high particle charge, previously described in the literature for the electrophoretic mobility, and also the relaxation processes occurring in a wide frequency range and their consequences on the complex electric dipole moment induced on the particles by the oscillating electric field. As we already pointed out in a recent paper regarding the dynamic electrophoretic mobility of a colloidal particle in a salt-free concentrated suspension, the competition between these relaxation processes is decisive for the dielectric response throughout the frequency range of interest. Finally, we examine the dielectric response of highly charged particles in more depth, because some singular electrokinetic behaviors of salt-free suspensions have been reported for such cases that have not been predicted for salt-containing suspensions.     

Synthesis and characterization of charged polystyrene-acrylic acid latex particles

Novel, monodisperse charged colloidal particles of polystyrene cross linked with divinylbenzene and surface-grafted with acrylic acid were synthesized by emulsion polymerization and were characterized by estimating the dissociable surface charge by conductivity titration, the particle effective charge by conductivity verses particle concentration, and the particle size by dynamic light scattering and atomic force microscopy. The structural ordering and dynamics were investigated as a function of the volume fraction of the particles using static and dynamic light scattering, respectively. Furthermore, from the electrophoresis measurements, these particles are found to have a high salt tolerance due to increases in charge as a function of salt concentration.     

Electronic and geometric properties of Au nanoparticles on Highly Ordered Pyrolytic Graphite (HOPG) studied using X-ray Photoelectron Spectroscopy (XPS) and Scanning Tunneling Microscopy (STM)

Au nanoparticles grown on mildly sputtered Highly Ordered Pyrolytic Graphite (HOPG) surfaces were studied using Scanning Tunneling Microscopy (STM) and X-ray Photoelectron Spectroscopy (XPS). The results were compared with those of Ag nanoparticles on the same substrate. By varying the defect densities of HOPG and the Au coverages, one can create Au nanoparticles in various sizes. At high Au coverages, the structures of the Au films significantly deviate from the ideal truncated octahedral form: the existence of many steps between different Au atomic layers can be observed, most likely due to a high activation barrier of the diffusion of Au atoms across the step edges. This implies that the particle growth at room temperature is strongly limited by kinetic factors. Hexagonal shapes of Au structures could be identified, indicating preferential growth of Au nanostructures along the (111) direction normal to the surface. In the case of Au, XPS studies reveal a weaker core level shift with decreasing particle size compared to the 3d level in similarly sized Ag particles. Also taking into account the Auger analysis of the Ag particles, the core level shifts of the metal nanoparticles on HOPG can be understood in terms of the metal/substrate charge transfer. Ag is (partially) positively charged, whereas Au negatively charged on HOPG. It is demonstrated that XPS can be a useful tool to study metal-support interactions, which plays an important role for heterogeneous catalysis, for example.     

Highly charging of nanoparticles through electrospray of nanoparticle suspension

Patterned deposition of nanoparticles is a prerequisite for the application of unique properties of nanoparticles in future nanodevices. Recent development of nanoxerography requires highly charged aerosol nanoparticles to avoid noise deposition due to random Brownian motion. However, it has been known that it is difficult to charge aerosol nanoparticles with more than two elementary charges. The goal of this work is to develop a simple technique for obtaining highly charged monodisperse aerosol nanoparticles by means of electrospray of colloidal suspension. Highly charged aerosol nanoparticles were produced by electrospraying (ES) and drying colloidal suspensions of monodisperse gold nanoparticles. Size and charge distributions of the resultant particles were measured. We demonstrate that this method successfully charges monodisperse nanoparticles very highly, e.g., 122 elementary charges for 25.0 nm, 23.5 for 10.5 nm, and 4.6 for 4.2 nm. The method described here constitutes a convenient, reliable, and continuous tool for preparing highly charged aerosol nanoparticles from suspensions of nanoparticles produced by either wet chemistry or gas-phase methods.     

Nanoparticle assembly on patterned "plus/minus" surfaces from electrospray of colloidal dispersion

Selective deposition of metal (Au) and oxide (SiO2) nanoparticles with a size range of 10-30 nm on patterned silicon-silicon oxide substrate was performed using the electrospray method. Electrical charging characteristics of particles produced by the electrospray and patterned area created by contact charging of the electrical conductor with non- or semi-conductors were investigated. Colloidal droplets were electrosprayed and subsequently dried as individual nanoparticles which then were deposited on substrates, and observed using field emission-scanning electron microscopy. The number of elementary charge units on particles generated by the electrospray was 0.4-148, and patterned area created by contact charging contained sufficient negative charges to attract multiple charged particles. Locations where nanoparticles were (reversibly) deposited depended on voltage polarity applied to the spraying colloidal droplet and the substrate, and the existence of additional ions such as those from a stabilizer.     

Selective dissolution of the silver component in colloidal Au and Ag multilayers: a facile way to prepare nanoporous gold film materials

Colloidal Au/Ag multilayer films were prepared by alternate assembly of Au nanoparticles with a size of 5 +/- 1.2 nm and Ag nanoparticles with a size of 10 +/- 2.4 nm by using 1,5-pentanedithiol as cross-linker. Nanoporous gold films with a ligament size of 26.7 +/- 4.6 nm were then prepared by selective dissolution of sacrificial templates of silver particles in colloidal Au/Ag multilayers. The complete dissolution of Ag particles in colloidal Au/Ag multilayers in a mixture solution of 3.0 mM HAuCl(4) and 3 M NaCl took place at room temperature without damage of the colloidal Au film. This method to prepare nanoporous gold films was further extended to the preparation of nanoporous gold nanotubes by depositing colloidal Au/Ag film on the inner wall of anodic aluminum oxides (AAO) followed by dissolution of colloidal Ag and removal of AAO templates.     

Effect of anionic surfactants on synthesis and self-assembly of silica colloidal nanoparticles

Effects of the anionic surfactants, sodium dodecyl sulfate and sodium oleate, on the formation and properties of silica colloidal nanoparticles were investigated. At a concentration of approximately 1 x 10(-3) M, adsorption of anionic surfactants increased particle size, monodispersity, and negative surface charge density of synthesized silica particles. As uniformity of particle size and particle-particle interactions increase, colloidal photonic crystals readily self-assemble without extensive washing of the synthesized silica nanoparticles. The photonic crystals diffract light in the visible region according to Bragg's law. The assembled colloidal particle arrays exhibit a face-centered cubic structure in dried thin films. This study offers a new approach for producing ordered colloidal silica thin films.     

Polarizability and complex conductivity of dilute suspensions of spherical colloidal particles with charged (polyelectrolyte) coatings

The dielectric relaxation of polyelectrolyte-coated colloidal particles is examined via "exact" numerical solutions of the governing electrokinetic equations. The charged polymer coatings are characterized by a nominal charge density, thickness, and permeability. Brush-like segment density profiles are considered here, but more sophisticated segment and charge density profiles are accommodated by the model. The role of added counterions and nonspecific adsorption is considered briefly before examining how the experimentally measured conductivity and dielectric constant increments reflect the frequency of the applied electric field, the strength of the electrolyte, and characteristics of the polymer coatings, namely the charge, charge density, and permeability. Finally, a strategy is suggested by which dielectric spectroscopy and electrophoresis can be used to characterize polymer-coated particles. This approach complements experiments where electroviscous effects such as dynamic light scattering and sedimentation are weak.     

Surface molecular imprinting on polypropylene fibers for rhodamine B selective adsorption

The interaction between silver nanoparticles (Ag NPs) of different surface charge and surfactants relevant to the laundry cycle has been investigated to understand changes in speciation, both in and during transport from the washing machine. Ag NPs were synthesized to exhibit either a positive or a negative surface charge in solution conditions relevant for the laundry cycle (pH 10 and pH 7). These particles were characterized in terms of size and surface charge and compared to commercially laser ablated Ag NPs. The surfactants included anionic sodium dodecylbenzenesulfonate (LAS), cationic dodecyltrimethylammoniumchloride (DTAC) and nonionic Berol 266 (Berol). Surfactant-Ag NP interactions were studied by means of dynamic light scattering, Raman spectroscopy, zeta potential, and Quartz Crystal Microbalance. Mixed bilayers of CTAB and LAS were formed through a co-operative adsorption process on positively charged Ag NPs with pre-adsorbed CTAB, resulting in charge reversal from positive to negative zeta potentials. Adsorption of DTAC on negatively charged synthesized Ag NPs and negatively charged commercial Ag NPs resulted in bilayer formation and charge reversal. Weak interactions were observed for nonionic Berol with all Ag NPs via hydrophobic interactions, which resulted in decreased zeta potentials for Berol concentrations above its critical micelle concentration. Differences in particle size were essentially not affected by surfactant adsorption, as the surfactant layer thicknesses did not exceed more than a few nanometers. The surfactant interaction with the Ag NP surface was shown to be reversible, an observation of particular importance for hazard and environmental risk assessments.     

Charging and stability of anionic latex particles in the presence of linear poly(ethylene imine)

Charging properties and colloidal stability of negatively charged polystyrene latex particles were investigated in the presence of linear poly(ethylene imine) (LPEI) of different molecular masses by electrophoresis and dynamic light scattering (DLS). Electrophoretic mobility measurements illustrate that LPEI strongly adsorbs on these particles leading to charge neutralization at isoelectric point (IEP) and charge reversal. Time-resolved DLS experiments indicate that the aggregation of the latex particles is rapid near the IEP and slows down away from this point. Surprisingly, the colloidal stability does not depend on the molecular mass, which indicates that the adsorbed LPEI layer is rather homogeneous.     

Manipulating the optical properties of pyramidal nanoparticle arrays

This paper reports the orientation-dependent optical properties of two-dimensional arrays of anisotropic metallic nanoparticles. These studies were made possible by our simple procedure to encapsulate and manipulate aligned particles having complex three-dimensional (3D) shapes inside a uniform dielectric environment. Using dark field or scattering spectroscopy, we investigated the plasmon resonances of 250-nm Au pyramidal shells embedded in a poly(dimethylsiloxane) (PDMS) matrix. Interestingly, we discovered that the scattering spectra of these particle arrays depended sensitively on the direction and polarization of the incident white light relative to the orientation of the pyramidal shells. Theoretical calculations using the discrete dipole approximation support the experimentally observed dependence on particle orientation with respect to incident field. This work presents an approach to manipulate--by hand--ordered arrays of particles over cm(2) areas and provides new insight into the relationship between the shape of well-defined, 3D particles and their supported plasmon resonance modes.     

Light-induced aggregation of colloidal gold nanoparticles capped by thymine derivatives

The colloid stability of thymine-coated gold nanoparticles under light irradiation as a function of particle size, surface charge, and exposure time was investigated in alkaline, aqueous solutions as well as in a 0.5 vol % of DMF in H(2)O mixture. With increasing exposure to light irradiation at 280 nm, more and more particles coagulated. Light-induced aggregation of colloidal gold nanoparticles was attributed to reorientation of thymine terminal groups tethered on gold particle surfaces. A smaller particle size and negatively charged surface reduced the rate of photodimerization or even inhibited the photoreaction. UV-vis and FTIR spectroscopy confirmed the photodimerization of terminal thymine molecules under 280 nm light irradiation. The reaction kinetics of thymine photodimerization appears to be a combination of first-order reactions, each having different rates, reflecting the inhomogeneity and high curvature of the gold nanoparticle surfaces.     

Effective charges of colloidal particles obtained from collective diffusion experiments

In this work, the collective diffusion coefficient of highly charged colloidal particles in dilute dispersions has been measured by means of dynamic light scattering. The possibility of obtaining valuable information about the particle charge from these data is looked into with the help of electrophoresis experiments. Our results suggest that this is possible in the case of slight or moderately interacting particles as long as experimental data are properly treated. For highly interacting colloids, however, such information could not be so reliable, presumably due to certain shortcomings of the experimental technique at low angle. The role of charge renormalization is also discussed in this work.     

Effect of mixing on the formation of complexes of hyperbranched cationic polyelectrolytes and anionic surfactants

The effect of different mixing protocols on the charged nature and size distribution of the aqueous complexes of hyperbranched poly(ethylene imine) (PEI) and sodium dodecyl sulfate (SDS) was investigated by electrophoretic mobility and dynamic light scattering measurements at different pH values, polyelectrolyte concentrations, and ionic strengths. It was found that at large excess of the surfactant a colloidal dispersion of individual PEI/SDS nanoparticles forms via an extremely rapid mixing of the components by means of a stop-flow apparatus. However, the application of a less efficient mixing method under the same experimental conditions might result in large clusters of the individual PEI/SDS particles as well as in a more extended precipitation regime compared with the results of stop-flow mixing protocol. The study revealed that the larger the charge density and concentration of the PEI, the more pronounced the effect of mixing becomes. It can be concluded that an efficient way to avoid precipitation in the solutions of oppositely charged polyelectrolytes and surfactants might be provided by extending the range of kinetically stable colloidal dispersion of polyelectrolyte/surfactant nanoparticles via the application of appropriate mixing protocols.     

Charge renormalization of charged spheres based on thermodynamic properties

At strong electrostatic coupling, counterions are accumulated in the vicinity of the surface of the charged particle with intrinsic charge Z. In order to explain the behavior of highly charged particles, effective charge Z(*) is therefore invoked in the models based on Debye-Huckel approximation, such as the Derjaguin-Landau-Verwey-Overbeek potential. For a salt-free colloidal suspension, we perform Monte Carlo simulations to obtain various thermodynamic properties omega in a spherical Wigner-Seitz cell. The effect of dielectric discontinuity is examined. We show that at the same particle volume fraction, counterions around a highly charged sphere with Z may display the same value of omega as those around a weakly charged sphere with Z(*), i.e., omega(Z)=omega(Z(*)). There exists a maximally attainable value of omega at which Z=Z(*). Defining Z(*) as the effective charge, we find that the effective charge passes through a maximum and declines again due to ion-ion correlation as the number of counterions is increased. The effective charge is even smaller if one adopts the Debye-Huckel expression omega(DH). Our results suggest that charge renormalization can be performed by chemical potential, which may be observed in osmotic pressure measurements.     

Polyelectrolyte-templated synthesis of bimetallic nanoparticles

Bimetallic nanoparticles (NPs) are known to exhibit enhanced optical and catalytic properties that can be optimized by tailoring NP composition, size, and morphology. Galvanic deposition of a second metal onto a primary metal NP template is a versatile method for fabricating bimetallic NPs using a scalable, solution-based synthesis. We demonstrate that the galvanic displacement reaction pathway can be controlled through appropriate surface modification of the NP template. To synthesize bimetallic Au-Ag NPs, we used colloidal Ag NPs modified by layer-by-layer (LBL) assembled polyelectrolyte layers to template the reduction of HAuCl(4). NPs terminated with positively and negatively charged polyelectrolytes yield highly contrasting morphologies and Au surface concentrations. We propose that these charged surface layers control galvanic charge transfer by controlling nucleation and diffusion at the deposition front. This surface-directed synthetic strategy can be advantageously used to tailor both overall NP morphology and Au surface concentrations.     

Ultra‐Stable Plasmonic Colloidal Aggregates for Accurate and Reproducible Quantitative SE(R)RS in Protein‐Rich Biomedia

Au/Ag colloids aggregated with simple salts are amongst the most commonly used substrates in surface‐enhanced (resonance) Raman spectroscopy (SE(R)RS). However, salt‐induced aggregation is a dynamic process, which means that SE(R)RS enhancements vary with time and that measurements therefore need to be taken at a fixed time point, normally within a short time‐window of a few minutes. Here, we present an emulsion templated method which allows formation of densely‐packed quasi‐spherical Au/Ag colloidal aggregates. Since the particles in the product aggregates retain their weakly adsorbed charged ligands and the ionic strength remains low these charged aggregates resist further aggregation while still providing intense SE(R)RS enhancement which remains stable for days. This eliminates a major source of irreproducibility in conventional colloidal SE(R)RS measurements and paves the way for SE(R)RS analysis in complex systems, such as protein‐rich bio‐solutions where conventional aggregated colloids fail.     

Layered magnetite nanoparticles modification – synthesis,structure, and magnetic characterization

Core-shell and multilayered nanoparticles based on magnetite core with different metallic spacing and over-layers are prepared in one pot synthesis and characterized. The spacer layers were made from Au, Cu or Ag precursors. The nanoparticles were fabricated by a modified chemical seed based method. The obtained nanoparticles were examined by X-ray diffraction, Energy-dispersive X-ray spectroscopy, Transmission Electron Microscopy, Differential Scanning Calorimetry and Infrared spectroscopy. Magnetic properties of the nanoparticles were tested by Mössbauer spectroscopy and Magnetometry. Magnetization and Mössbauer measurements show that the presence of the metallic layers influences the magnetic state of the particles. XRD and EDX confirm layered structures of nanoparticles. Proposed synthesis allows for fabrication of layered particles with controlled morphology and register properties changes which are related to the nature of each subsequent layer.