Rings of bundled single‐walled carbon nanotubes with perfectly toroidal geometries (see figure), are fabricated in high yields by a floating chemical vapor deposition process involving the thermal decomposition of acetylene. The nanotube rings can be grown with varying densities on a wide variety of substrates at relatively low temperatures, which is a significant advantage for nanoelectronics applications.

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ZnO nanoneedle arrays have been grown on a large scale with a chemical vapor deposition method at 680 degrees C. Zn powder and O(2) gas are employed as source materials, and catalyst-free Si plates are used as substrates. Energy-dispersive X-ray and X-ray diffraction analyses show that the nanoneedles are almost pure ZnO and preferentially aligned in the c-axis direction of the wurtzite structure. The growth mechanism of ZnO nanoneedle arrays is discussed with the thermodynamic theory and concluded to be the result of the co-effect of the surface tension and diffusion. Photoluminescence spectrum of the as-grown products shows a strong emission band centering at about 484 nm, which originates from oxygen vacancies. Field-emission examination exhibits that the ZnO nanoneedle arrays have a turn-on voltage at about 5.3 V/microm.

At a low temperature of 450 degrees C, ZnS nanoribbons have been synthesized on Si and KCl substrates by a simple chemical vapor deposition (CVD) method with a two-temperature-zone furnace. Zinc and sulfur powders are used as sources in the different temperature zones. X-ray diffraction (XRD), selected area electron diffraction (SEAD), and transmission electron microscopy (TEM) analysis show that the ZnS nanoribbons are the wurtzite structure, and there are two types-single-crystal and bicrystal nanoribbons. Photoluminescence (PL) spectrum shows that the spectrum mainly includes two parts: a purple emission band centering at about 390 nm and a blue emission band centering at about 445 nm with a weak green shoulder around 510 nm.

A highly efficient direct electrodeposition method was used to prepare Co-Cu alloy nanotubes in an anodic alumina template without modification. The morphology and structure of as-prepared Co-Cu nanotubes were examined by scanning electron microscopy, transmission electron microscopy, and X-ray diffraction. The formation mechanism of the tubular nanostructure is discussed. It was found that the template directed electrodeposition of Co-Cu at a large current density can result in the highly efficient growth of nanotubes and that the growth rate as well as the wall thickness of the nanotubes can be controlled via the current density of electrodeposition. Magnetic measurements of the Co-Cu nanotube array show that the nanotubes are ferromagnetic at room temperature and may find potential applications in the fields of biological separation and drug delivery.

Synthesis and optical properties of ZnO-ZnS core-shell nanotube arrays

Large quantities of indium nitride (InN) nanowires are synthesized by the in situ nitriding of indium oxide (In(2)O(3)) powders in an ammonia (NH(3)) flux. Tens of milligrams of nanowires are obtained in one batch. Every 100 mg of In(2)O(3) starting powder can produce up to 65 mg of InN nanowires under the optimized conditions. The synthesized nanowires grow along the [001] direction with excellent crystallinity. They are of high purity and are 30-50 microm in length with an almost uniform diameter of about 100 nm. Photoluminescence measurements of the nanowires exhibit a strong peak at 707 nm. An optical bandgap of about 1.7 eV is estimated based on the absorption spectrum. The experimental results also demonstrate that the approach of nitriding In(2)O(3) powders in situ is feasible for the synthesis of high-purity InN nanowires in large quantities, with good reproducibility and without catalyst materials. The synthesis of InN nanowires in large quantities would be of benefit to the further study and understanding of their intrinsic properties, as well as being advantageous for their potential application in nanodevices.

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