Ice Nucleation on a Corrugated Surface.

Heterogeneous ice nucleation is a key process in many environmental and technical fields and is of particular importance in modeling atmospheric behavior and the Earth's climate. Despite an improved understanding of how water binds at solid surfaces, no clear picture has emerged to describe how 3D ice grows from the first water layer, nor what makes a particular surface efficient at nucleating bulk ice. This study reports how water at a corrugated, hydrophilic/hydrophobic surface restructures from a complex 2D network, optimized to match the solid surface, to grow into a continuous ice film.

Two-Dimensional Wetting of a Stepped Copper Surface.

Highly corrugated, stepped surfaces present regular 1D arrays of binding sites, creating a complex, heterogeneous environment to water. Rather than decorating the hydrophilic step sites to form 1D chains, water on stepped Cu(511) forms an extended 2D network that binds strongly to the steps but bridges across the intervening hydrophobic Cu(100) terraces. The hydrogen-bonded network contains pentamer, hexamer, and octomer water rings that leave a third of the stable Cu step sites unoccupied in order to bind water H down close to the step dipole and complete three hydrogen bonds per molecule.

A general method for controlling and resolving rotational orientation of molecules in molecule-surface collisions.

The outcome of molecule-surface collisions can be modified by pre-aligning the molecule; however, experiments accomplishing this are rare because of the difficulty of preparing molecules in aligned quantum states. Here we present a general solution to this problem based on magnetic manipulation of the rotational magnetic moment of the incident molecule. We apply the technique to the scattering of H from flat and stepped copper surfaces.

How Atomic Steps Modify Diffusion and Inter-adsorbate Forces: Empirical Evidence from Hopping Dynamics in Na/Cu(115).

We followed the collective atomic-scale motion of Na atoms on a vicinal Cu(115) surface within a time scale of pico- to nanoseconds using helium spin echo spectroscopy. The well-defined stepped structure of Cu(115) allows us to study the effect that atomic steps have on the adsorption properties, the rate for motion parallel and perpendicular to the step edge, and the interaction between the Na atoms. With the support of a molecular dynamics simulation we show that the Na atoms perform strongly anisotropic 1D hopping motion parallel to the step edges.