High-coercivity FePt nanoparticle assemblies embedded in silica thin films.

The ability to process assemblies using thin film techniques in a scalable fashion would be a key to transmuting the assemblies into manufacturable devices. Here, we embed FePt nanoparticle assemblies into a silica thin film by sol-gel processing. Annealing the thin film composite at 650 degrees C transforms the chemically disordered fcc FePt phase into the fct phase, yielding magnetic coercivity values H(c)>630 mT. The positional order of the particles is retained due to the protection offered by the silica host. Such films with assemblies of high-coercivity magnetic particles are attractive for realizing new types of ultra-high-density data storage devices and magneto-composites.

Effect of nanoparticles on sessile droplet contact angle.

This paper investigates the change in contact angle of droplets of fluid containing dispersed nanoparticles (nanofluid) functionalized with thioglycolic acid molecules as a function of the concentration and size of nanoparticles, and the quality and composition of the substrate material. Bismuth telluride nanoparticles with an average size ranging from 2.5 to 10.4 nm and functionalized with thioglycolic acid groups were grown by a microemulsion method and dispersed in water. Experimental measurements of the contact angle of nanofluid droplets cast on smooth glass and silicon substrates show that the contact angle depends strongly on nanoparticle concentration. Moreover, smaller size nanoparticles lead to larger changes in contact angle at the same mass concentration. These findings contribute to understanding the role of functionalized nanoparticles in surface wettability.

Irradiation-induced magnetism in carbon nanostructures.

Nitrogen (15N) and carbon (12C) ion implantations with implant energy of 100 keV for different doses were performed on nanosized diamond (ND) particles. Magnetic measurements on the doped ND show ferromagnetic hysteresis behavior at room temperature. The saturation magnetization (M(s)) in the case of 15N implanted samples was found to be higher compared to the 12C implanted samples for dose sizes greater than 10(14) cm(-2). The role of structural modification or defects along with the carbon-nitrogen (C-N) bonding states for the observed enhanced ferromagnetic ordering in 15N doped samples is explained on the basis of x-ray photoelectron spectroscopy measurements.

ZnO nanowires by pulsed laser vaporization: synthesis and properties.

We report a new pulsed-laser vaporization (PLV) technique to synthesize nanowires of single-crystal ZnO having a wurtzite structure by using colloidal gold nanoparticles as seeding catalysts. The average diameter of the nanowires is approximately 13 nm, with a very narrow range of 7 to 25 nm. The nanowires are straight for the most part, with the axes parallel to the [0001] growth direction. Raman and photoluminescence spectra from the nanowires and bulk ZnO are similar except for a approximately 510 nm band in the nanowires due to oxygen vacancies. The bulk-like vibrational and electronic properties of the nanowires is due to the diameter being larger than the threshold below which quantum confinement-induced effects are expected.

Wet-chemical templateless assembly of metal nanowires from nanoparticles.

We describe a new, simple, room-temperature wet-chemical approach for assembling Au and Ag nanoparticles into nanowire networks, without the use of lithographic templates. Five to 35 nm-diameter nanowires passivated with a thin organic layer were synthesized by mechanically agitating a biphasic liquid mixture of an aqueous hydrosol containing the nanoparticles, and toluene. Nanowire structure and surface chemistry are discussed based on electron microscopy, UV-visible spectroscopy and thermogravimetric analyses.

Templateless room-temperature assembly of nanowire networks from nanoparticles.

We demonstrate a new, room-temperature approach to assemble two-dimensional and three-dimensional networks of gold nanowires by agitating nanoparticles in a toluene-aqueous mixture, without the use of templates. The nanowires have a uniform diameter of about 5 nm and consist of coalesced face-centered cubic nanocrystals. Toluene molecules passivate the gold surfaces during nanoparticle coalescence, rendering the nanowires hydrophobic and enabling their transfer into the toluene layer. Such templateless low-temperature assembly of mesostructures from nanoscale building blocks open up new possibilities for creating porous self-supporting nanocatalysts, nanowires for device interconnection, and low-density high-strength nanofillers for composites.

Microfabrication technology: organized assembly of carbon nanotubes.

Nanoscale structures need to be arranged into well-defined configurations in order to build integrated systems. Here we use a chemical-vapour deposition method with gas-phase catalyst delivery to direct the assembly of carbon nanotubes in a variety of predetermined orientations onto silicon/silica substrates, building them into one-, two- and three-dimensional arrangements. The preference of nanotubes to grow selectively on and normal to silica surfaces forces them to inherit the lithographically machined template topography of their substrates, allowing the sites of nucleation and the direction of growth to be controlled.

Carbon nanotube-magnesium oxide cube networks.

For future applications based on carbon nanotubes, two- and three-dimensional architectures of nanotubes need to be assembled. In many cases this will involve the creation of nanotube units and nodes from which these nanotubes can be distributed in a network. We demonstrate that this idea is plausible by using a template of the correct dimensions and shape, and that has facets that provide the right growth conditions: submicrometer-sized MgO cubes are used to grow nanotubes by chemical vapor deposition. The resulting networks often show that the MgO cubes function as distribution sites for arrays of aligned nanotubes.