Expanding micelle nanolithography to the self-assembly of multicomponent core-shell nanoparticles.

Size, composition, and pattern formation are crucial elements in the fabrication of functional multicomponent nanoparticles (NPs). Self-assembly techniques provide relevant control over NP size distribution (down to a few nanometers in diameter), but more importantly, such techniques are amenable for practical applications since the resulting NPs (and arrays thereof) are programmed in the molecular structure of the precursors. Here, the diblock copolymer micelle nanolithography concept of achieving monodisperse NPs is extended to direct the synthesis of multicomponent core-shell NPs arranged in a triangular lattice.

Low-temperature growth of silicon nanotubes and nanowires on amorphous substrates.

Silicon one-dimensional (Si 1D) materials are of particular relevance due to their prospect as versatile building materials for nanoelectronic devices. We report the growth of Si 1D structures from quasi-hexagonally ordered gold (Au) nanoparticle (NP) arrays on borosilicate glass (BSG) and SiOx/Si substrates. Using hydrogen instead of oxygen plasma during NP preparation enhances the catalytic activity of AuNPs (diameters of 10-20 nm), enabling Si 1D growth at temperatures as low as 320 degrees C.

Selective growth of organic 1-D structures on au nanoparticle arrays.

We demonstrate that the growth of F16CuPc 1-D nanostructures can be directed by templates of gold nanoparticles. The growth occurs via vapor-phase transport, whereby the gold nanoparticles act as nucleation sites for F16CuPc molecules and promote their anisotropic growth. The F16CuPc 1-D structures adopt diameters of approximately 15-30 nm independent of the nanoparticle size.