To better understand N-2 formation in the selective catalytic reduction of
NOx by propene under oxidative atmosphere, we studied the catalytic behavio
r of bimetallics. Surface segregation phenomena may provoke geometric and e
lectronic modifications of the catalytic active sites. To explain our resul
ts we invoked: (i) the facile way to oxidize the bimetallic aggregates, (ii
) the presence of atoms with low coordination number able to be oxidized fi
rst and (iii) an eventual formation of like "vic-diNO(x) species" on such b
imetallics leading to N-2 formation.