T. Visart de Bocarmé

Oxygen adsorption on gold nanofacets and model clusters

We have studied oxygen interaction with Au crystals (field emitter tips) using time-resolved (atom-probe) field desorption mass spectrometry. The results demonstrate no adsorption to take place on clean Au facets under chosen conditions of pressures (p < 10(-4) m/bar) and temperatures (T = 300-350 K). Steady electric fields of 6 V/nm do not allow dissociating the oxygen molecule. The measured O2+ intensities rather reflect ionization of O2 molecules at critical distances above the Au tip surface. Certain amounts of Au-O2 complex ions can be found at the onset of Au field evaporation. Calculations by density functional theory (DFT) show weak oxygen end-on interaction with Au10 clusters (Delta E = 0.023 eV) and comparatively stronger interaction with Au1/Au(100) model surfaces (Delta E = 0.25 eV). No binding is found on {210} facets. Including (positive) electric fields in the DFT calculations leads to an increase of the activation energy for oxygen dissociation thus providing an explanation for the absence of atomic oxygen ions from the field desorption mass spectra.

Surface segregation of Au-Pd alloys in UHV and reactive environments : Quantification by a catalytic atom probe

The surface composition of an Au-62at%Pd alloy has been studied by means of a catalytic atom probe (CAP) before and after exposures to nitric oxide (NO) at temperatures ranging from 300 to 573K for 20min. Subsequent CAP analysis at 100K revealed a considerable surface enrichment in Pd (to approximately 80at%) after exposure at 573K. This is correlated with the occurrence of NO dissociation, and the formation of strong Pd-O bonds at the surface. Blank experiments in ultra-high vacuum reflect the surface composition of the bulk material, in excellent agreement with electron microprobe analysis. At 573K, no detectable surface segregation occurs in the absence of NO adsorption for the times and temperatures studied. However, classical Metropolis Monte-Carlo simulations performed with a semi-empirical potential on the Au(40)Pd(60) (111), (110) and (100) systems show surface enrichment of gold at equilibrium. This suggests that the temperatures of the clean surface segregation experiments are too low to reach equilibrium within times of the order of hours.

CO Oxidation on Gold Surfaces Studied on the Atomic Scale

The interaction of small gold crystal tips with oxygen gas and CO/O2 gas mixtures was studied by means of field ion microscopy (FIM). High-resolution FIM-images of clean tips were obtained with hydrogen and neon as imaging gas. At temperatures between 300 and 450 K the exposure of a clean Au sample to O2 gas at 100–1000 mbar, in the absence of an electric field, led to oxygen chemisorption and formation of a “surface oxide”. The presence of an electric field of 12–15 V/nm was found to enhance the oxidation process. Exposure to CO gas at 300 K led to the removal of the surface oxide. This was associated with the occurrence of a wave front which started in the apex centre and extended to the outskirts of the tip sample. The build-up of the surface oxide and its titration by carbon monoxide was completely reversible. Our results strongly suggest that pure gold crystals are active catalysts for the CO oxidation at 300 K.

Catalytic reduction of NO2 with hydrogen on Pt field emitter tips: kinetic instabilities on the nanoscale.

The catalytic reduction of NO(2) with hydrogen on a Pt field emitter tip is investigated using both field electron microscopy (FEM) and field ion microscopy (FIM). A rich variety of nonlinear behavior and unusually high catalytic activity around the {012} facets are observed. Our FEM investigations reveal that the correlation function exhibits damped oscillations with a decaying envelope, showing that molecular noise will influence the dynamics of the oscillations. The dependence of the oscillatory period on the P(H(2))/P(NO(2)) pressure ratios is analyzed. Similar patterns are reported under FIM conditions. Corresponding density functional theory (DFT) calculations for the adsorption of NO(2) on Pt{012} in the presence of an external electric field are performed in order to gain an atomistic understanding of the underlying nonlinear phenomena.

In situ dynamic study of hydrogen oxidation on rhodium.

The reaction of hydrogen/oxygen gas mixtures with rhodium single crystals was studied using video-FIM (Field Ion Microscopy) at temperatures between 350 and 550 K and up to 2 x 10(-2) Pa total pressure. Imaging at 500 K in a hydrogen rich gas mixture (H2:O2 = 9) revealed considerable morphological changes of the (0 0 1)-oriented field emitter tip, i.e. the growth of low-index at the expense of high-index planes and strong crystal coarsening. Decreasing the hydrogen partial pressure led to chemical and structural changes of the Rh sample. Starting on the [1 1 0] planes a surface oxide formed, which spread anisotropically across the surface until it finally covered the whole visible surface area. The transformation was reversible upon increasing the hydrogen pressure back to its initial value. However, a hysteresis behavior was observed, i.e. a larger hydrogen partial pressure was found to be necessary to re-establish the initial patterns of a reactive Oad/Had layer. By varying the temperature from 400 to 500 K a phase diagram was established for the Oad/Had system. Increasing the electric field proved to shift the phase diagram towards higher H2 pressures. At 550K self-sustained kinetic oscillations with a cycle time of approximately 40s could be observed.

Field-induced CO adsorption and formation of carbonyl waves on gold nanotips

We report a study of the adsorption and reaction of CO on a gold nanotip in high electrostatic fields. Field ion microscopy is used to investigate the emergence of a Au-carbonyl wave that is made visible with oxygen as the imaging gas. We set up a simple kinetic model that reproduces the adsorption wave and confirms that the presence of oxygen merely serves as an imaging gas and does not lead to field-induced oxidation of CO.

Hydrogenation of NO and NO2 over palladium and platinum nanocrystallites: case studies using field emission techniques

In this work, we investigate the catalytic hydrogenation of NO over palladium and platinum and of NO2 over platinum surfaces. Samples are studied using field emission techniques including field emission/ion microscopies (FEM/FIM). The aim of this study is to obtain detailed information on the non-linear dynamics during NOx hydrogenation over nanocrystallites at the atomic scale. The interaction between Pd and pure NO has been studied between 450 K and 575 K and shows the dissociative adsorption of NO. After the subsequent addition of hydrogen in the chamber, a surface reaction with the oxygen-adlayer can be observed. This phenomenon is reversible upon variation of the H2 pressure, exhibits a strong hysteresis behaviour but does not show any unstable regime when control parameters are kept constant. On platinum, NO is dissociated and the resulting O(ads) layer can also react with H2. Although occurring on both Pd and Pt metals, the reaction mechanism seems to be different. On palladium, NO dissociation takes place on the whole visible surface area leading to a “surface oxide” that can be reacted off by raising the H2 pressure whereas on Pt, the catalytic reaction is self-sustained and restricted to 〈001〉 zone lines comprising {011} and {012} facets and where self-triggered surface explosions are observed. Two kinetic phase diagrams were established for the NO–H2 reaction over palladium and platinum samples under similar experimental conditions. Their shapes reflect a different chemical reactivity of metal surfaces towards oxygen species resulting from the dissociation of NO. NO2 hydrogenation is followed over Pt samples and shows self-sustained kinetic instabilities that are expressed as peaks of brightness that are synchronized over the whole active area (corresponding to the 〈001〉 zone lines as in the NO case) within 40 ms, the time resolution of the video-recorder used for this work.

Field ion microscopy study of the structural changes in Rh crystals during the reaction of oxygen-hydrogen gas mixtures

The interaction of oxygen/hydrogen gas mixtures with Rh crystals was studied by means of video-FIM (field ion microscopy) at temperatures between 400 and 500 K and total pressures up to 10 -2 Pa. Rh samples were found to suffer considerable morphological changes during the reaction at 505 K and relative gas amounts of H 2 /O 2 = 0.1…9. Strong faceting of planes lying along the zone lines was seen and interpreted as being oxygen-driven. The surface structures changed while removing hydrogen from the gas mixture. In situ video-FIM allowed us to monitor the time dependence of changes. Accordingly, planes lying along the zone lines transformed first from O ad /H ad into O ad -covered The process started in {011 } planes and finally reached the (001) pole. A cross-like image feature thus appeared and divided the apex surface of the Rh crystal into four equivalent quadrants with {111 } planes in their center. These quadrants reacted subsequently in an independent manner, that is, the transformation from an O ad /H ad mixed layer into an O ad layer occurred with a delay period of up to several minutes while decreasing the hydrogen gas pressure. The structural changes observed were reversible upon increasing the hydrogen gas pressure.

The role of fluctuations in bistability and oscillations during the H2 + O2 reaction on nanosized rhodium crystals.

A combined experimental and theoretical study is presented of fluctuations observed by field ion microscopy in the catalytic reaction of water production on a rhodium tip. A stochastic approach is developed to provide a comprehensive understanding of the different phenomena observed in the experiment, including burst noise manifesting itself in a bistability regime, noisy oscillations, and nanopatterns with a cross-like oxidized zone separating the surface into four quadrants centered on the {111} facets. The study is based on a stochastic model numerically simulating the processes of adsorption, desorption, reaction, and transport. The surface diffusion of hydrogen is described as a percolation process dominated by large clusters corresponding to the four quadrants. The model reproduces the observed phenomena in the ranges of temperature, pressures, and electric field of the experiment.

C2H2 interaction with Ni nanocrystals: towards a better understanding of carbon nanotubes nucleation in CVD synthesis.

We present a study of the early stages of carbon nanotubes nucleation in CVD synthesis by combining field ion/electron emission microscopy (FIM/FEM) and atom-probe investigation (AP) of the nickel-carbon interaction. Acetylene decomposition on Ni tips at 873K is observed to induce additional step formation on an initially facetted (polyhedral) crystal. Carbon-enriched steps are then observed to act as preferential nucleation centers of graphene sheets formation. Atom-probe experiments reveal C(2) and C(3) species and frequency dependent studies demonstrate that the origin of these species is different from C(1). Experiments provide clear evidence for the crucial role of carbon-enriched steps as nucleation sites of graphene sheets on the Ni surface.