Surface morphology controls water dissociation on hydrated IrO2 nanoparticles

Abstract

Iridium oxide is a highly efficient catalyst for the oxygen evolution reaction, whose large-scale application requires decreasing the metal content. This is achieved using small nanoparticles. The knowledge of the water–IrO₂ nanoparticle interface is of high importance to understand the IrO₂ behavior as electrocatalyst in aqueous solutions. In this contribution, DFT (PBE-D2) calculations and AIMD simulations on IrO₂ nanoparticle models of different sizes ((IrO₂)₃₃ and (IrO₂)₁₁₅) are performed. Results show that two key factors determine the H₂O adsorption energy and the preferred adsorption structure (molecular or dissociated water): metal coordination and hydrogen bonding with oxygen bridge atoms of the IrO₂ surface. Regarding metal coordination, and since the tetragonal distortion existing in IrO₂ is retained on the nanoparticle models, the adsorption at iridium axial vacant sites implies stronger Ir–H₂O interactions, which favors water dissociation. In contrast, Ir–H₂O interaction at equatorial vacant sites is weaker and thus the relative stability of molecular and dissociated forms becomes similar. Hydrogen bonding increases adsorption energy and favors water dissociation. Thus, tip and corner sites of the nanoparticle, with no oxygen bridge atoms nearby, exhibit the smallest adsorption energies and a preference for the molecular form. Overall, the presence of rather isolated tip and corner sites in the nanoparticle leads to lower adsorption energies and a smaller degree of water dissociation when compared with extended surfaces.