Optimization of Active Sites via Crystal Phase, Composition, and Morphology for Efficient Low‐Iridium Oxygen Evolution Catalysts

Abstract

Reducing the amount of iridium in oxygen evolution electrocatalysts without compromising their catalytic performances is one of the major requirements in proton-exchange-membrane water electrolyzers. Herein, with the help of theoretical studies, we show that anatase-type TiO₂ -IrO₂ solid solutions possess more active iridium catalytic sites for the oxygen evolution reaction (OER) than IrO₂ , the benchmark OER catalyst. Note that the same is not observed for their rutile-type counterparts. However, owing to their thermodynamic metastability, anatase-type TiO₂ -IrO₂ solid solutions are generally hard to synthesize. Our theoretical studies demonstrate that such catalytically active anatase-type solid-solution phases can be created in situ on the surfaces of readily available SrTiO₃ -SrIrO₃ solid solutions during electrocatalysis in acidic solution as the solution can etch away Sr atoms. We experimentally show this with porous SrTiO₃ -SrIrO₃ solid-solution nanotubes synthesized by a facile synthetic route that contain 56 % less iridium than IrO₂ yet show an order of magnitude higher apparent catalytic activity for OER in acidic solution.