Ferroelectric-Based Catalysis: Switchable Surface Chemistry

Abstract

The maximum efficiency of a fixed catalytic surface occurs when the adsorbate-surface interaction strength is optimal as per the Sabatier principle: strong enough to drive the reactions forward but weak enough to permit the products' desorption. Such a compromise can fundamentally limit catalytic activity. One solution is to create a surface with switchable activity between strong binding (rapid dissociation) and weak binding (easy desorption). On the basis of first-principles theory, we describe a class of catalysts comprising an epitaxial monolayer of a transition metal oxide on an oxide ferroelectric substrate in which reversing the ferroelectric polarization state switches the surface activity between these two limits. As an example, a CrO 2 monolayer on ferroelectric PbTiO 3 permits direct NO x decomposition and CO oxidation while circumventing oxygen and sulfur poisoning. Our computed binding energy trends are explained by a generalization of the canonical d-band model for transition metals to metal oxide surfaces combined with charge transfer effects.