Carbon supported iridium-octaethylporphyrin (IrOEP), iridium-tetraphen
ylporphyrin (IrTPP) and iridium-phthalocyanine (IrPc) were studied in
acid for the oxygen reduction. Both porphyrins give a four-electron re
duction, although a peculiar deactivation at low potentials occurs. At
IrPc and heat treated porphyrins hydrogen peroxide is formed. Results
are compared with carbon monoxide oxidation experiments at these cata
lysts. A single site mechanism is proposed for the oxygen reduction me
chanism.