Efficient oxygen evolution electrocatalysis in acid by a perovskite with face-sharing IrO ₆ octahedral dimers

Abstract

The widespread use of proton exchange membrane water electrolysis requires the development of more efficient electrocatalysts containing reduced amounts of expensive iridium for the oxygen evolution reaction (OER). Here we present the identification of 6H-phase SrIrO ₃ perovskite (6H-SrIrO ₃) as a highly active electrocatalyst with good structural and catalytic stability for OER in acid. 6H-SrIrO ₃ contains 27.1 wt% less iridium than IrO ₂, but its iridium mass activity is about 7 times higher than IrO ₂, a benchmark electrocatalyst for the acidic OER. 6H-SrIrO ₃ is the most active catalytic material for OER among the iridium-based oxides reported recently, based on its highest iridium mass activity. Theoretical calculations indicate that the existence of face-sharing octahedral dimers is mainly responsible for the superior activity of 6H-SrIrO ₃ thanks to the weakened surface Ir-O binding that facilitates the potential-determining step involved in the OER (i.e., O* + H ₂O → HOO* + H ⁺ +  e _¯).

Abstract

While splitting water may provide a renewable source of carbon-neutral energy, the water oxidation half-reaction is sluggish and the materials needed show poor stability. Here, authors demonstrate an unusual iridium-based oxide to perform high-efficiency oxygen evolution in acid with good stability.