Abstract
AbstractThe selective catalytic reduction (SCR) of NOx with NH3 to N2 with supported V2O5(‐WO3)/TiO2 catalysts is an industrial technology used to mitigate toxic emissions. Long‐standing uncertainties in the molecular structures of surface vanadia are clarified, whereby progressive addition of vanadia to TiO2 forms oligomeric vanadia structures and reveals a proportional relationship of SCR reaction rate to [surface VOx concentration]2, implying a 2‐site mechanism. Unreactive surface tungsta (WO3) also promote the formation of oligomeric vanadia (V2O5) sites, showing that promoter incorporation enhances the SCR reaction by a structural effect generating adjacent surface sites and not from electronic effects as previously proposed. The findings outline a method to assess structural effects of promoter incorporation on catalysts and reveal both the dual‐site requirement for the SCR reaction and the important structural promotional effect that tungsten oxide offers for the SCR reaction by V2O5/TiO2 catalysts.
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