Wafer-scale development, characterization, and high temperature stabilization of epitaxial Cr2O3 films grown on Ru(0001).

This work outlines conditions suitable for the heteroepitaxial growth of Cr2O3(0001) films (1.5-20 nm thick) on a Ru(0001)-terminated substrate. Optimized growth is achieved by sputter deposition of Cr within a 4 mTorr Ar/O2 20% ambient at Ru temperatures ranging from 450 to 600 °C.

DFT Investigation of Ammonia Formation via a Langmuir-Hinshelwood Mechanism on Mo-Terminated δ-MoN(0001).

In this work, we employed density functional theory to elucidate the energetics associated with elementary steps along a Langmuir-Hinshelwood mechanism for the Haber-Bosch synthesis of ammonia from N and H on a hexagonal, Mo-terminated molybdenum nitride surface. Using nudged elastic band calculations, we determined the energy barriers involved in the reaction processes. An active site consisting of four nearest-neighbor Mo atoms, previously identified as an active site on similar surfaces, was chosen to investigate the reaction processes.

Insights into Silica Bilayer Hydroxylation and Dissolution.

Hydroxylation and dissolution of well-structured silica bilayer films grown on a ruthenium single-crystal support (SiO/Ru(0001)) was studied by temperature programmed desorption and X-ray photoelectron spectroscopy (XPS). Water desorption signals from SiO/Ru(0001) hydroxylated by electron-bombardment of adsorbed ice at 100 K were found to be comparable to those of hydroxylated bulk silica samples and attributed to adsorbed molecular water and silanol groups (vicinal and terminal). Isotopic exchange between O-labeled SiO and O-labeled water suggests the occurrence of dynamic siloxane bond cleavage and re-formation during electron bombardment.

Electron stimulated hydroxylation of a metal supported silicate film.

Water adsorption on a double-layer silicate film was studied by using infrared reflection-absorption spectroscopy, thermal desorption spectroscopy and scanning tunneling microscopy. Under vacuum conditions, small amounts of silanols (Si-OH) could only be formed upon deposition of an ice-like (amorphous solid water, ASW) film and subsequent heating to room temperature. Silanol coverage is considerably enhanced by low-energy electron irradiation of an ASW pre-covered silicate film.

Ultrathin silica films: the atomic structure of two-dimensional crystals and glasses.

For the last 15 years, we have been studying the preparation and characterization of ordered silica films on metal supports. We review the efforts so far, and then discuss the specific case of a silica bilayer, which exists in a crystalline and a vitreous variety, and puts us into a position to investigate, for the first time, the real space structure (AFM/STM) of a two-dimensional glass and its properties. We show that pair correlation functions determined from the images of this two-dimensional glass are similar to those determined by X-ray and neutron scattering from three-dimensional glasses, if the appropriate sensitivity factors are taken into account.

Model oxide-supported metal catalysts--comparison of ultrahigh vacuum and solution based preparation of Pd nanoparticles on a single-crystalline oxide substrate.

Using single-crystalline Fe(3)O(4)(111) films grown over Pt(111) in UHV as a model-support, we have characterized the nucleation behaviour and chemical properties of Pd particles grown over the film using different deposition techniques with scanning tunnelling microscopy and X-ray photoelectron spectroscopy. Comparison of Pd/Fe(3)O(4) samples created via Pd evaporation under UHV conditions and those resulting from the solution deposition of Pd-hydroxo complexes reveals that changes in the interfacial functionalization of such samples (i.e.

Thin silica films on Ru(0001): monolayer, bilayer and three-dimensional networks of [SiO4] tetrahedra.

The atomic structure of thin silica films grown over a Ru(0001) substrate was studied by X-ray photoelectron spectroscopy, infrared reflection absorption spectroscopy, low energy electron diffraction, helium ion scattering spectroscopy, CO temperature programmed desorption, and scanning tunneling microscopy in combination with density functional theory calculations. The films were prepared by Si vapor deposition and subsequent oxidation at high temperatures. The silica film first grows as a monolayer of corner-sharing [SiO(4)] tetrahedra strongly bonded to the Ru(0001) surface through the Si-O-Ru linkages.

CO adsorption and desorption on size-selected Pd(n)/TiO2(110) model catalysts: size dependence of binding sites and energies, and support-mediated adsorption.

The nature of CO adsorption on Pd(n)/TiO(2)(110) (n = 1, 2, 7, 20) has been examined using temperature-programmed desorption (TPD), temperature-dependent helium ion scattering (TD-ISS), and X-ray photoelectron spectroscopy (XPS). All samples contain the same number of Pd atoms (0.10 ML-equivalent) deposited as different size clusters.

Size-dependent oxygen activation efficiency over Pd(n)/TiO2(110) for the CO oxidation reaction.

The dissociative binding efficiency of oxygen over Pd(n)/TiO(2)(110) (n = 4, 7, 10, 20) has been measured using temperature programmed reaction (TPR) mass spectrometry and X-ray photoemission spectroscopy (XPS) following exposure to O(2) with varying doses and dose temperatures. Experiments were carried out following two different O(2) exposures at 400 K (10 L and 50 L) and for 10 L of O(2) exposure at varying temperatures (T(surf) = 200, 300, and 400 K). During TPR taken after sequential O(2) and CO (5 L at 180 K) exposures, unreacted CO is found to desorb in three features at T(desorb) ≈ 150, 200, and 430 K, while CO(2) is observed to desorb between 170 and 450 K.

Electronic structure controls reactivity of size-selected Pd clusters adsorbed on TiO2 surfaces.

The catalytic activity of metal clusters of different sizes adsorbed on oxide surfaces can be explored systematically by using model catalysts. We studied the temperature-programmed reaction of CO with O2 catalyzed by Pd clusters (Pd(n), for n = 1, 2, 4, 7, 10, 16, 20, and 25) that were size-selected in the gas phase and deposited on rutile TiO2(110). X-ray photoemission spectroscopy revealed that the Pd 3d binding energy varied nonmonotonically with cluster size and that the changes correlated with strong size variations in CO oxidation activity.