Temperature programmed desorption (TPD), Auger electron spectroscopy (AES), X-ray photoelectron spectroscopy (XPS), and scanning tunneling microscopy (STM) have been used to characterize molybdenum carbide nanoparticles prepared on a Au(111) substrate. The MoC(x) nanoparticles were formed by Mo metal deposition onto a reactive multilayer of ethylene, which was physisorbed on a Au(111) substrate at low temperatures (<100 K). The resulting clusters have an average diameter of approximately 1.5 nm and aggregate in the fcc troughs located on either side of the elbows of the reconstructed Au(111) surface. Core level XPS shows that the electronic environment of the Mo and C atoms in the nanoparticles is similar to that found in Mo(2)C(0001) single crystals and carburized Mo metal surfaces. Peak intensities in XPS and AES spectra were used to estimate an average Mo/C atomic ratio of 1.2 +/- 0.3 for nanoparticles annealed above 600 K.

We report on an scanning tunneling microscopy study of the nanocrystallite phases of TiO(2) formed via reactive-layer-assisted deposition in ultrahigh vacuum. The synthesis used reaction of a thin layer of water, on a Au(111) substrate at 130 K, with low-coverage vapor-deposited Ti. The effects of annealing temperature and reactant coverage were investigated. Large-scale (>20 nm) patterns in the surface distribution of nanoparticles were observed with the characteristic length-scale of the pattern correlating with the thickness of the initial layer of H(2)O. The phenomenon is explained as being due to the formation of droplets of liquid water at temperatures between 130 and 300 K. After the surface was annealed to 400 K, the individual titania nanoparticles formed by this process had diameters of 0.5-1 nm. When the surface was annealed to higher temperatures, nanoparticles coalesced and for annealing temperatures of 900 K compact nanocrystals formed with typical dimensions of 5-20 nm. Three distinct classes of nanocrystallites were observed and their atomic structure and composition investigated and discussed.

Arrays of highly strained 5-25 nm-wide regions have been prepared on rutile TiO2(110) surface through a low energy Ar ion bombardment technique. Using scanning tunneling microscopy (STM) and an innovative STM tip-triggered nanoexplosion approach we show experimentally that the protrusions arise from subsurface Ar-filled pockets. Continuum mechanics modeling gives good estimates of the corresponding elastic deformation. Surface strain values of up to 4% have been deduced.