A Low-Energy Ion Scattering Approach for Studying Au Nanoclusters Grown on an H2O Buffer Layer.

A novel form of alkali low-energy ion scattering is used to probe the deposition of nanoclusters onto a solid surface via buffer layer assisted growth (BLAG) in ultrahigh vacuum. A thin amorphous solid water (ASW) buffer layer is grown on a TiO2(110) single crystal cooled to 100 K. Au atoms deposited onto this layer arrange themselves into nanoclusters. The sample is then annealed to 320 K to desorb the ASW and enable the clusters to soft-land onto the substrate. Time-of-flight low-energy ion scattering, using Li+, Na+, and K+ projectiles, probes the materials during each step of the BLAG process to measure the surface composition and reveal the details of how the clusters form. The neutralization probability of Na+ ions singly scattered from the Au nanoclusters indicates that they increase in size after annealing and that the magnitude of the increase is a function of the buffer layer thickness. The adsorption of a thin, incomplete water layer prior to Au deposition forms nanoclusters that are possibly even smaller than those produced by direct deposition onto the clean substrate.

Surface termination of cleaved Bi2Se3 investigated by low energy ion scattering.

It has been widely assumed that Se terminates the surface of the topological insulator, bismuth selenide. Although some Se is initially at the surface after cleaving at 80 K, low energy ion scattering reveals a complete Bi termination at room temperature. Density functional theory shows that a Bi bilayer atop the bulk-terminated structure is energetically favorable. It is thus proposed that a thermally activated process induces a spontaneous termination change after cleaving. This has profound implications on the electrical transport and long-term stability of such materials and devices.

Correlated electron effects in low energy Sr(+) ion scattering.

Resonant charge transfer during low energy ion scattering reveals correlated-electron behavior at high temperature. The valence electron of a singly charged alkaline-earth ion is a magnetic impurity that interacts with the continuum of many-body excitations in the metal, leading to Kondo and mixed valence resonances near the Fermi energy. The occupation of these resonances is acutely sensitive to the surface temperature, which results in a marked temperature dependence of the ion neutralization. We report such a dependence for low energy Sr(+) scattered from polycrystalline gold.

Ion beam induced formation and interrogation of Au nanoclusters.

Low-energy ion bombardment of a Au thin film by 0.5 keV Ar+ forms self-organized nanoclusters that display quantum size effects. The reduction of Au coverage with sputtering time is quantified with x-ray photoemission spectroscopy, and a decrease of both the rms roughness and correlation length is measured by STM. Neutralization of scattered 3 keV Na+ and K+ alkali-metal ions is used to probe the electronic states of the sputter-induced nanoclusters. The neutral fractions gradually increase as the cluster dimensions decrease, indicating that the electronic structure is similar to that of clusters grown by deposition.

Li ion scattering from Au nanoclusters on TiO2(110).

The neutralization of low energy 7Li+ scattered from Au nanoclusters deposited on TiO2(110) was measured with time-of-flight spectroscopy as a function of cluster size, emission angle, and ion energy. The neutralization shows maxima for cluster diameters approximately 3 nm, and again for thick Au films. The data are compared to previous experiments with Na projectiles. Possible explanations of the observed effects are discussed.

Charge exchange in Li scattering from Si surfaces.

Neutral fractions are measured for 4 keV 7Li(+) scattering from clean, hydrogen-covered, and cesiated Si surfaces. The neutral fraction in scattering from clean Si is approximately 26% and it decreases with hydrogen adsorption. When Cs is adsorbed on Si, the neutral fraction does not distinguish the local potential at the Cs sites from the Si sites, unless hydrogen is coadsorbed. These results demonstrate that resonant charge transfer occurs due to coupling of the Li ionization level with the dangling bond surface states, and that the influence of the dangling bonds extends beyond the local scattering sites.

Detection of quantum confined states in au nanoclusters by alkali ion scattering.

Charge state-resolved time-of-flight spectra were collected for 2.0 keV 23Na+ scattered from Au nanoclusters deposited on TiO2(110). The neutral fraction of Na scattered from metallic Au is low ( approximately 3%), but it is surprisingly high (up to 50%) for small clusters. The results demonstrate that alkali ions couple to electronic states specific to the nanoclusters, and that the energy of the states is a function of the nanocluster size. This technique provides a new method for the spectroscopy of nanomaterials.

Surface-reconstruction-switched adsorbate photofragmentation dynamics.

Energy-resolved angular distributions of neutral fragments ejected during photoinduced electron transfer reaction of CH3Br on GaAs(100) exhibit three distinct methyl-radical ejection channels. These undergo marked changes when the termination is switched from the Ga-rich c(8 x 2) to the As-rich c(2 x 8). Our observations are consistent with a strong adsorption-site dependence of the dynamics.