Direct Visualization and Control of Atomic Mobility at {100} Surfaces of Ceria in the Environmental Transmission Electron Microscope.

Ceria is one of the world's most prominent material for applications in heterogeneous catalysis, as catalyst support or catalyst itself. Despite an exhaustive literature on the structure of reactive facets of CeO2 in line with its catalytic mechanisms, the temporal evolution of the atomic surface structure exposed to realistic redox conditions remains elusive. Here, we provide a direct visualization of the atomic mobility of cerium atoms on {100} surfaces of CeO2 nanocubes at room temperature in high vacuum, O2, and CO2 atmospheres in an environmental transmission electron microscope. Through quantification of the cationic mobility, we demonstrate the control of the surface dynamics under exposure to O2 and CO2 atmospheres, providing opportunities for a better understanding of the intimate catalytic mechanisms.

Preparation and comparison of supported gold nanocatalysts on anatase, brookite, rutile, and P25 polymorphs of TiO2 for catalytic oxidation of CO.

Nanosized anatase (< or = 10 nm), rutile (< or = 10 nm), and brookite (approximately 70 nm) titania particles have been successfully synthesized via sonication and hydrothermal methods. Gold was deposited with high dispersion onto the surfaces of anatase, rutile, brookite, and commercial titania (P25) supports through a deposition-precipitation (D-P) process. All catalysts were exposed to an identical sequence of treatment and measurements of catalytic CO oxidation activity. The as-synthesized catalysts have high activity with concomitant Au reduction upon exposure to the reactant stream. Mild reduction at 423 K produces comparably high activity catalysts for every support. Deactivation of the four catalysts was observed following a sequence of treatments at temperatures up to 573 K. The brookite-supported gold catalyst sustains the highest catalytic activity after all treatments. XRD and TEM results indicate that the gold particles supported on brookite are smaller than those on the other supports following the reaction and pretreatment sequences.

Uniform formation of uranium oxide nanocrystals inside ordered mesoporous hosts and their potential applications as oxidative catalysts.

Highly dispersed uranium oxide nanocrystals supported on ordered mesoporous silica matrixes with large surface areas and porosities have been synthesized via a co-assembly methodology; the preliminary catalysis tests showed that these materials have a high catalytic activity for the thermal oxidation of volatile organic compounds (VOCs).

Quantum antidot formation and correlation to optical shift of gold nanoparticles embedded in MgO.

Quantum antidots are subnanometer scale vacancy clusters, the localized electronic structure of which can significantly alter the properties of a nanomaterial. We use positron spectroscopy to study vacancy clusters generated during the formation of gold nanoparticles via ion implantation in an MgO matrix. We observed that quantum antidots are associated with the nanoparticle surfaces after annealing in an O2 atmosphere, but not after annealing in a H2 atmosphere. In the former case, the presence of quantum antidots bound to the gold nanoparticles correlates with the redshift of the gold surface plasmon resonance, thus allowing an explanation for the redshift based on the transfer of electrons away from the metal particles.