One-dimensional nanostructures of SnO 2 with a ribbonlike morphology have been prepared in large scale via rapid oxidation of elemental tin at 1080 °C. The products were characterized with scanning electron microscopy, X-ray powder diffraction, transmission electron microscopy, Raman scattering, and photoluminescence spectroscopy. The as-synthesized SnO 2 nanoribbons appeared to be single crystals and had preferred [110] and [203] growth directions. The lengths of the nanoribbons were up to several hundreds of micrometers, and the typical width and thickness were in the range of 30-150 nm and 10-30 nm, respectively. The strong photoluminescence of the nanoribbons in the visible region suggested possible applications in nanoscaled optoelectronic devices. A possible growth mechanism for the SnO 2 nanoribbons was proposed.

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We report the growth of ultrathin diamond nanorods (DNRs) by a microwave plasma assisted chemical vapor deposition method using a mixture gas of nitrogen and methane. DNRs have a diameter as thin as 2.1 nm, which is not only smaller than reported one-dimensional diamond nanostructures (4-300 nm) but also smaller than the theoretical value for energetically stable DNRs. The ultrathin DNR is encapsulated in tapered carbon nanotubes (CNTs) with an orientation relation of (111)diamond//(0002)graphite. Together with diamond nanoclusters and multilayer graphene nanowires/nano-onions, DNRs are self-assembled into isolated electron-emitting spherules and exhibit a low-threshold, high current-density (flat panel display threshold: 10 mA/cm2 at 2.9 V/microm) field emission performance, better than that of all other conventional (Mo and Si tips, etc.) and popular nanostructural (ZnO nanostructure and nanodiamond, etc.) field emitters except for oriented CNTs. The forming mechanism of DNRs is suggested based on a heterogeneous self-catalytic vapor-solid process. This novel DNRs-based integrated nanostructure has not only a theoretical significance but also has a potential for use as low-power cold cathodes.

Uniform and porous graphene nanoflake films (GNFs) have been investigated as a support for catalytic Pt nanoclusters in direct methanol electro-oxidation. Pt nanoclusters of varying thickness are deposited on GNFs using magnetron sputtering, and their effects on the electrocatalytic activity for oxidizing methanol are systemically studied. GNF supported Pt nanoclusters with ultralow catalyst loading exhibit high performance for methanol electrocatalytic oxidation with a large mass-specific peak current density and a ratio of forward to backward peak currents up to 1.4. These characteristics compare favorably to the majority of Pt-C based electrodes, except for those of carbon nanotubes with Pt decoration on both the inner and the outer wall surfaces. The results obtained are ascribed to a highly coupled network made of high-density 2-4 nm Pt monolayer nanoclusters on both the basal and edge planes of each nanoflakes of graphene. GNFs are a promising support material for developing next-generation advanced Pt based fuel cells and their relevant electrodes in the field of energy.