Direct reaction of adsorbed molecular oxygen with hydrazine on a clean Pt(111) surface

The oxidation of hydrazine on the clean Pt(lll) surface has been investigated by temperature-programmed reaction spectroscopy (TPRS) in the temperature range 130-800 Ii. Direct reaction of molecular oxygen is observed on the Pt(111) surface for the first time, as indicated by the desorption of nitrogen beginning at 130 Ii with a maximum rate at 145 Ii, below the molecular oxygen dissociation temperature, Direct reaction of hydrazine with adsorbed molecular oxygen results in the formation of water and nitrogen. With excess hydrazine, all surface oxygen is reacted, forming water. When only adsorbed atomic oxygen is present, the low-temperature nitrogen yield decreases by a factor of 3 and the peak nitrogen desorption temperature increases to 170 K, No high-temperature (450-650 K) nitrogen desorption characteristic of nitrogen atom recombination is seen indicating that during oxidation the nitrogen-nitrogen bond in hydrazine remains intact, as observed previously for hydrazine decomposition on the Pt(111) surface and hydrazine oxidation on rhodium. Two water desorption peaks are observed. characteristic of desorption-limited (175 K) and reaction-limited (200 K) water evolution from the Pt(lll) surface. For low coverages of hydrazine, only the reaction-limited water desorption is observed, previously attributed to water formed from adsorbed hydroxyl groups. When excess hydrazine is adsorbed. the usual hydrazine decomposition products, H-2, N-2 and NH3, are also observed. No nitrogen oxide species (NO, NO2 and N2O) were observed in these experiments, even when excess oxygen was available on the surface.