Adsorption of acrolein and its hydrogenation products on Cu(111).

The adsorption of acrolein and its hydrogenation products propanal, 1-propanol, and 2-propenol on Cu(111) was studied by reflection absorption infrared spectroscopy (RAIRS) and temperature-programmed desorption (TPD). The experimental RAIR spectra were obtained by adsorbing multilayers of each molecule at 85 K and then annealing the surface up to 200 K to desorb the multilayer and produce the most stable monolayer structure on the surface. Each of the four molecules adsorbs weakly to the surface and desorbs at temperatures below 225 K.

Dissociation of Single O Molecules on Ag(110) by Electrons, Holes, and Localized Surface Plasmons.

A detailed understanding of the dissociation of O molecules on metal surfaces induced by various excitation sources, electrons/holes, light, and localized surface plasmons, is crucial not only for controlling the reactivity of oxidation reactions but also for developing various oxidation catalysts. The necessity of mechanistic studies at the single-molecule level is increasingly important for understanding interfacial interactions between O molecules and metal surfaces and to improve the reaction efficiency. We review single-molecule studies of O dissociation on Ag(110) induced by various excitation sources using a scanning tunneling microscope (STM).

Dissociation Mechanism of a Single O Molecule Chemisorbed on Ag(110).

The dissociation of O molecules chemisorbed on silver surfaces is an essential reaction in industry, and the dissociation mechanism has long attracted attention. The detailed dissociation mechanism was studied at the single-molecule level on Ag(110) by using a scanning tunneling microscope (STM). The dissociation reaction was found to be predominantly triggered by inelastically tunneled holes from the STM tip due to the significantly distributed density of states below the Fermi level of the substrate.

The influence of palladium on the hydrogenation of acetylene on Ag(111).

We have used reflection absorption infrared spectroscopy (RAIRS) and temperature programmed reaction (TPR) to study the selective hydrogenation of acetylene on both a clean Ag(111) surface and on a Pd/Ag(111) single-atom-alloy surface. The partial hydrogenation of acetylene to ethylene is an important catalytic process that is often carried out using PdAg alloys. It is challenging to study the reaction with ultrahigh vacuum techniques because H does not dissociate on Ag(111), and while H will dissociate at Pd sites, H-atom spillover from Pd to Ag sites does not generally occur.