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This paper describes a simple, one-pot method that generates dimers of silver nanospheres in one step without any additional assembly steps. The dimers are consisted of single-crystal silver nanospheres ∼30 nm in diameter and separated by a gap of 1.8 nm wide. The key to the success of this method lies in the control of colloidal stability and oxidative etching by optimizing the amount of chloride added to a polyol synthesis. The dimers provide a well-defined system for studying the hot spot phenomenon (hot spot: the gap region of a pair of strongly coupled silver or gold nanoparticles), an extremely important but poorly understood subject in surface-enhanced Raman scattering (SERS). Because of the relatively small size of the silver nanospheres, only those molecules trapped in the hot spot region are expected to contribute to the detected SERS signals. By correlating SERS measurements with SEM imaging, we found that the SERS enhancement factor within the hot spot region of such a dimer was on the order of 2 × 107. [ABSTRACT FROM AUTHOR]

We report a facile and environmentally friendly method of preparing highly branched silver nanostructures. By reducing AgNO 3with l-ascorbic acid in an aqueous solution, silver particles having a coral-like morphology were formed in a few minutes. A mechanistic study of the growth process revealed that the silver branches grew from a bulbous seed formed through aggregation, and that by changing the concentrations of the reagents, the degree of particle branching could be altered. With their potentially high surface areas, these branched structures could find use as catalysts or as substrates for surface-enhanced Raman scattering applications. [ABSTRACT FROM AUTHOR]

This paper describes the use of methoxy-poly(ethylene glycol) silane (MPEG-sil) as a linker molecule for the synthesis of silica-coated nanoparticles by the Stöber method. While short alkane chain-based siloxanes including (acryloxypropyl)trimethoxysilane and 3-methacryloxypropyl-trimethoxysilane are popular molecules used in surface modification, they are not efficient for the silica coating of nanoparticles synthesized from organic solvents containing long carbon chain carboxylic acids or amines as capping agents. Here, we report the utilization of MPEG-sil to bridge this gap. Our approach is based on a two-phase system, in which ligand exchange takes place in a hydrophobic environment and the surface modification with silica is conducted in an ethanol−water mixture. Our results show that this two-phased approach was effective to coat monodisperse Fe 2O 3nanoparticles capped with oleic acid and Ag nanoparticles capped with oleylamine with uniform SiO 2shells. The process was also demonstrated for double-shell nanostructures to produce SiO 2-coated Pt@Fe 2O 3core−shell nanoparticles. The results described in this work represent a new approach for the surface modification with silica coating of monodisperse nanoparticles synthesized from nonhydrolytic solutions and can potentially have a broad ramification in the development of water-dispersible nanoparticles for biological applications. [ABSTRACT FROM AUTHOR]

This article describes a simple approach to anisotropic Au nanostructures with various shapes by reducing HAuCl 4with poly(vinyl pyrrolidone) (PVP) in aqueous solutions without the use of any additional capping agent or reductant. In this approach, the commercially available PVP servers as a mild reducing agent thanks to its hydroxyl (−OH) end groups, enabling kinetic control over both nucleation and growth. As the volume of HAuCl 4solution added to the reaction was increased, the morphology of Au nanostructures evolved from nanotadpoles to nanokites and then triangular and hexagonal microplates. The slow reduction rate associated with the mild reducing power of PVP plays a critical role in forming nanoplates during nucleation as well as their growth into highly anisotropic nanostructures. Electron microscopy studies reveal that the nanotadpoles and nanokites are formed through the linear fusion of small Au particles (<10 nm) to the initially formed nanoplates, whereas the microplates result from the continuous addition of Au atoms to the side faces of nanoplates. Through this morphological control, the localized surface plasmon resonance peaks of these Au nanostructures can be tuned in the visible and near-IR regions. [ABSTRACT FROM AUTHOR]

This paper describes a cation exchange approach to the synthesis of metal chalcogenide core−shell particles with the same size but a number of different compositions. This method begins with the preparation of colloidal spheres of amorphous Se (a-Se), followed by their reaction with Ag atoms to form SeAg2Se spheres. These core−shell spheres are then converted into SeMSe (M Zn, Cd, and Pb) via cation exchange with Zn2, Cd2, and Pb2. All the colloidal spheres prepared using this method are monodispersed in size and characterized by a spherical shape and a smooth surface. Starting from the same batch of SeAg2Se, the resultant SeMSe samples were essentially the same in size. Furthermore, these core−shell colloidal spheres can be easily made superparamagnetic by incorporating Fe3O4nanoparticles into the a-Se cores. This synthetic approach provides a simple and versatile route to magnetoactive core−shell spheres with the same size but a range of different compositions. This study also implies that it is feasible to further increase the diversity of cations that can be used in the cation exchange of a colloidal system to produce multifunctional core−shell spheres with a variety of properties. [ABSTRACT FROM AUTHOR]

This article describes a simple method for controlling the assembly of gold nanoparticles (Au NPs) into chainlike structures with tunable lengths and interparticle separations. The chainlike assemblies were induced to form by adding HS(CH2)nCOOH (n= 2, 10, and 15) into a suspension of Au NPs in a mixture of ethanol and water (98:2 by volume). The number of Au NPs in the chainlike assemblies could be altered by varying the concentration of the thiol while the interparticle distance between Au NPs in the chain could be adjusted by using thiols of different chain lengths. The chainlike assemblies of Au NPs were structurally unstable during storage and purification. We solved this problem by fixing the chainlike assemblies with silica coating via the Stöber method or by encapsulating them inside gelatin microspheres with the use of a fluidic device. After fixing, the chainlike assemblies of Au NPs could be preserved for a long period of time, during which their characteristic optical properties remained unchanged. [ABSTRACT FROM AUTHOR]

Pd−Pt core−shell nanoplates with hexagonal and triangular shapes were synthesized through the heterogeneous, epitaxial growth of Pt on Pd nanoplates. The Pd nanoplates were synthesized by reducing Na 2PdCl 4precursor with PVP as a reducing agent, which then served as seeds for the nucleation of Pt atoms formed by reducing H 2PtCl 6with citric acid. Characterization of the as-prepared Pd−Pt nanoplates by scanning transmission electron microscopy and high-resolution transmission electron microscopy reveals that a thin, uniform Pt shell was formed around the Pd nanoplate, demonstrating the layer-by-layer epitaxial growth of Pt on Pd surface in this approach. The close lattice match between Pd and Pt (lattice mismatch of only 0.77%) and the slow reduction rate associated with the mild reducing power of citric acid play key roles in achieving the epitaxial growth of Pt shells on Pd nanoplates. [ABSTRACT FROM AUTHOR]

Microscale fish bowls, hollow particles with engineered holes in their surfaces, were prepared using two different methods. In the first method, commercial latex beads suspended in water were swollen with a good solvent of the polymer, followed by freezing with liquid nitrogen and evaporation of the solvent below 0 °C. While one big hole was generated when the amount of solvent used for the swelling was relatively low, small holes could be produced in the outer surface of each bowl by increasing the degree of swelling. The porosity and pore structure show a similar dependence on the degree of swelling for both amorphous and semicrystalline polymers even though they are supposed to exhibit different phase behaviors during the freezing and solvent evaporation processes. In the second method, a polymer emulsion in water was prepared and then frozen with liquid nitrogen, followed by solvent evaporation below 0 °C. The porosity and pore structure could be controlled by adjusting the concentration of the polymer solution used to prepare the emulsion. As for encapsulation, the bowl-shaped particles could be transformed back into solid beads via thermal annealing at a temperature near the glass transition temperature of the polymer or by adding a good solvent of the polymer to the colloidal suspension. In a proof-of-concept experiment, microscale fish bowls were fabricated from poly(caprolactone), quickly loaded with a fluorescent dye, and sealed through thermal annealing. The encapsulated dye could then be slowly released in a phosphate buffered saline, suggesting their potential use as a new class of microscale capsules for drug delivery. [ABSTRACT FROM AUTHOR]

Highly faceted Pt nanocrystals with a large number of interconnected arms in a quasi-octahedral shape were synthesized simply by reducing H 2PtCl 6precursor with poly(vinyl pyrrolidone) in aqueous solutions containing a trace amount of FeCl 3. The iron species (Fe 3+or Fe 2+) play a key role in inducing the formation of the multioctahedral structure by decreasing the concentration of Pt atoms and keeping a low concentration for the Pt seeds during the reaction. This condition favors the overgrowth of Pt seeds along their corners and thus the formation of multiarmed nanocrystals. Electron microscopy studies revealed that the multioctahedral Pt nanocrystals exhibit a large number of edge, corner, and surface step atoms. The size of the multioctahedral Pt nanocrystals can be controlled by varying the concentration of FeCl 3added to the reaction and/or the reaction temperature. These multioctahedral Pt nanocrystals were tested as electrocatalysts for the oxygen reduction reaction in a proton exchange membrane fuel cell and exhibited improved specific activity and durability compared to commercial Pt/C catalyst. [ABSTRACT FROM AUTHOR]