Growth of nanocrystals and thin films at the water-oil interface.

The use of the water-oil interface provides significant advantages in the synthesis of inorganic nanostructures. Employing the water-toluene interface, luminescent CdS nanocrystals have been obtained at a relatively modest temperature of 35 degrees C. The diameters of the particulates can be varied between 1.0 and 5.0 nm. In addition, we have devised a new method for transferring thin films at the water-toluene interface onto solid substrates. Using this method, thin films consisting of Au and Ag nanocrystals spread over very large areas (square centimetres) are obtained in a single step. These films are directly usable as ingredients of functional devices. We show this by constructing a working amine sensor based on films of Au nanocrystals. The materials obtained have been characterized by X-ray diffraction, scanning and transmission electron microscopy, absorption and emission spectroscopy and charge transport measurements.

Phase control in the synthesis of magnetic iron sulfide nanocrystals from a cubane-type Fe-S cluster.

Phase control has been achieved in the synthesis of magnetic iron sulfide nanocrystals by the use of a single source precursor, a cubane type Fe-S cluster, bis(tetra-n-butylammonium) tetrakis[benezenethiolato-mu3-sulfido-iron]. This cluster cleanly decomposes in alkylamines to yield nanocrystals whose composition, structure, and dimensions are dependent on the temperature employed. At low temperatures, pyrrhotite type Fe7S8 nanocrystals with an average diameter of 5.6 nm are obtained. Higher temperatures yield griegite-Fe3S4 nanocrystals whose dimensions are tunable in the range 2.5-4.5 nm. All the obtained nanocrystals are superparamagnetic at room temperature.

Perpendicular magnetization in self-assembled films of citrate-capped gamma-Fe2O3 nanocrystals on Si(100) surfaces.

gamma-Fe2O3 nanocrystals capped with citrate and octylamine have been chemically prepared. The octylamine-capped nanocrystals exhibit a tendency to form ordered lattices. Films of nanocrystals of varying thickness (454, 720, and 1400 microg/cm2 in the case of citrate-capped nanocrystals and 300 microg/cm2 in the case of octylamine-capped nanocrystals) have been prepared on Si(100) substrates by drop casting and have been characterized by X-ray diffraction, scanning electron microscopy, and atomic force microscopy. Magnetic measurements have been carried out on the films as well as on nanocrystal powders. The films of citrate-capped gamma-Fe2O3 nanocrystals exhibit enhanced perpendicular magnetization, with the anisotropy depending on the film thickness.

Phase separation in metal oxides.

A fascinating phenomenon, recently found to occur in certain transition-metal oxides, is phase separation wherein pure, nominally monophasic oxides of transition metals with well-defined compositions separate into two or more phases over a specific temperature range. Such phase separation is entirely reversible, and is generally the result of a competition between charge-localization and -delocalization, the two situations being associated with contrasting electronic and magnetic properties. Coexistence of more than one phase, therefore, gives rise to electronic inhomogeneity and a diverse variety of magnetic, transport, and other properties, not normally expected of the nominal monophasic composition. An interesting feature of phase separation is that it covers a wide range of length scales anywhere between 1-200 nm. While cuprates and manganates, especially the latter, provide excellent examples of phase separation, it is possible that many other transition-metal compounds with extended structures will be found to exhibit phase separation.