A high-intensity electron gun based on field emission from a film of aligned carbon nanotubes has been made. The gun consists of a nanotube film with a 1-millimeter-diameter grid about 20 micrometers above it. Field-emission current densities of about 0.1 milliampere per square centimeter were observed for applied voltages as low as 200 volts, and current densities greater than 100 milliamperes per square centimeter have been realized at 700 volts. The gun is air-stable, easy and inexpensive to fabricate, and functions stably and reliably for long times (short-term fluctuations are on the order of 10 percent). The entire gun is only about 0.2 millimeter thick and can be produced with virtually no restrictions on its area, from less than 1 square millimeter to hundreds of square centimeters, making it suitable for flat panel display applications.

Molecular beam deflection measurements of small iron, cobalt, and nickel clusters show how magnetism develops as the cluster size is increased from several tens to several hundreds of atoms for temperatures between 80 and 1000 K. Ferromagnetism occurs even for the smallest sizes: for clusters with fewer than about 30 atoms the magnetic moments are atomlike; as the size is increased up to 700 atoms, the magnetic moments approach the bulk limit, with oscillations probably caused by surface-induced spin-density waves. The trends are explained in a magnetic shell model. A crystallographic phase transition from high moment to low moment in iron clusters has also been identified.

We report on the field emission properties of single-wall carbon nanotube films, with emphasis on current–versus–voltage (I–V) characteristics and current stability. The films are excellent field emitters, yielding current densities higher than 10 mA cm−2 with operating voltages that are far lower than for other film emitters, but show a significant degradation of their performances with time. The observed deviations from the Fowler-Nordheim behavior in the I–V characteristics point to the presence of a nonmetallic density of states at the tip of the nanotubes.

Carbon nanotube material can now be produced in macroscopic quantities. However, the raw material has a disordered structure, which restricts investigations of both the properties and applications of the nanotubes. A method has been developed to produce thin films of aligned carbon nanotubes. The tubes can be aligned either parallel or perpendicular to the surface, as verified by scanning electron microscopy. The parallel aligned surfaces are birefringent, reflecting differences in the dielectric function along and normal to the tubes. The electrical resistivities are anisotropic as well, being smaller along the tubes than perpendicular to them, because of corresponding differences in the electronic transport properties.

Open carbon nanotubes were filled with molten silver nitrate by capillary forces. Only those tubes with inner diameters of 4 nanometers or more were filled, suggesting a capillarity size dependence as a result of the lowering of the nanotube-salt interface energy with increasing curvature of the nanotube walls. Nanotube cavities should also be less chemically reactive than graphite and may serve as nanosize test tubes. This property has been illustrated by monitoring the decomposition of silver nitrate within nanotubes in situ in an electron microscope, which produced chains of silver nanobeads separated by high-pressure gas pockets.