We use surface second harmonic generation spectroscopy to study the oxidation of supported, size-selected silver clusters under ultra-high vacuum conditions. The oxidation reaction of small silver clusters between Ag9 and Ag55 is monitored by means of their localized surface plasmon resonance. We observe a rapid decline of the SH-intensity, as soon as cluster samples are exposed to an oxygen partial pressure of 5E-6 mbar, which is attributed to the formation of silver–oxygen-bonds. The evolution of the SH-intensity under exposure to oxygen shows a double-exponential character for all investigated cluster sizes. Since the oxidation of single crystalline silver surfaces follow single-exponential Langmuir-kinetics, the two independent pathways of SH-intensity loss are attributed to a surface- and an interface-oxidation of supported clusters, respectiveley. For small cluster sizes, a complete loss of the SH intensity is obtained, which suggests the complete oxidation of the clusters. For larger clusters a plasmonic resonance is still observed after oxidation, indicating a residual free-electron density.     «

We use surface second harmonic generation spectroscopy to study the oxidation of supported, size-selected silver clusters under ultra-high vacuum conditions. The oxidation reaction of small silver clusters between Ag9 and Ag55 is monitored by means of their localized surface plasmon resonance. We observe a rapid decline of the SH-intensity, as soon as cluster samples are exposed to an oxygen partial pressure of 5E-6 mbar, which is attributed to the formation of silver–oxygen-bonds. The evolution...     »