Dissociation of Single O 2 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). The comprehensive studies based on the STM and density functional theory calculations provide fundamental insights into the excitation pathway for the dissociation reaction.