In the present work, a generalization of some of the interpretations of het
erogeneous catalysis to the case of oxide film electrocatalysts has been at
tempted, using conductive boron-doped diamond supports. The very high stabi
lity of this material allowed the study of the catalytic properties of nobl
e-metal oxide modifications from the level of submonolayer to a few monolay
ers, avoiding the serious interference of the reactivity of the generally a
dopted metal supports. A mechanism for the chlorine evolution reaction at s
ubmonolayers of oxide electrocatalyst has been proposed, basing on a chlori
ne radical spillover stage.