Environment Controlled Dewetting of Rh−Pd Bilayers: A Route for Core−Shell Nanostructure Synthesis

Chemical environment plays a significant role on the size, shape, or surface composition of nanostructures. Here, the chemical environment effects are studied in the context of core−shell nanoparticle synthesis. The environment driven dynamics and kinetics of Rh/Pd bilayers is investigated by in situ ambient pressure X-ray photoelectron spectroscopy. Thin Rh (∼1.5 nm)/Pd (∼ 1.5 nm) bilayers were grown on thermally oxidized Si substrates. The films were heated in CO or NO environments or heated in vacuum with a subsequent NO/CO cycling. This study demonstrates that not the initial stacking sequence but the chemical environment plays a crucial role in controlling the surface composition. Heating in CO results in a surface enrichment of Pd at ∼200°C and is followed by film dewetting at ∼300 °C. Heating in NO results in progressive oxidation of Rh starting at ∼150 °C, which stabilizes the film continuity up to >∼375 °C. The film rupture correlates with the thermal destabilization of the surface oxide. Heating in vacuum results in a significant increase in surface Pd concentration, and the following NO/CO cycling induces periodic surface composition changes. The quasi-equilibrium states are ∼50% and ∼20% of Rh/(Rh + Pd) for NO and CO environments, respectively. Possible surface composition change and dewetting mechanisms are discussed on the basis of the interplay of thermodynamic (surface/oxide energy and surface wetting) and kinetic (surface oxidation and thermally induced and chemically enhanced diffusion) factors. The results open alternative ways to synthesize supported (core−shell) nanostructures with controlled morphology and surface composition.