Effect of ionic-bonding d0 cations on structural durability in barium iridates for oxygen evolution electrocatalysis

Abstract

Iridium has the exclusive chemistry guaranteeing both high catalytic activity and sufficient corrosion resistance in a strong acidic environment under anodic potential. Complex iridates thus attract considerable attention as high-activity electrocatalysts with less iridium utilization for the oxygen evolution reaction (OER) in water electrolyzers using a proton-exchange membrane. Here we demonstrate the effect of chemical doping on the durability of hexagonal-perovskite Ba_x(M,Ir)_yO_z-type iridates in strong acid (pH ~ 0). Some aliovalent cations are directly visualized to periodically locate at the octahedral sites bridging the two face-sharing [Ir₂O₉] dimer or [Ir₃O₁₂] trimers in hexagonal-perovskite polytypes. In particular, highly ionic bonding of the d⁰ Nb⁵⁺ and Ta⁵⁺ cations with oxygen anions results in notable suppression of lattice oxygen participation during the OER and thus effectively preserves the connectivity between the [Ir₃O₁₂] trimers without lattice collapse. Providing an in-depth understanding of the correlation between the electronic structure and bonding nature in crystals, our work suggests that proper control of chemical doping in complex oxides promises a simple but efficient tool to realize OER electrocatalysts with markedly improved durability.