Intrinsic properties of nanoparticulate Ir-based catalysts for oxygen evolution reaction by AC voltammetry.

Water splitting in acidic media is a sustainable and efficient new way to produce hydrogen fuel. However, the main bottleneck preventing the wider use of electrolyzers is still the oxygen evolution reaction (OER). Currently, the best electrocatalysts for OER are Ir-based materials, but the mechanistic details are still not fully understood. In this work, we investigate the similarities and differences in the OER mechanism of three different Ir-based catalysts, namely Vulcan carbon-supported and unsupported metallic Ir and rutile IrO 2 nanoparticles, and the process of Ir activation. For this purpose, we use large amplitude AC Voltammetry to distinguish between capacitive and faradaic processes. To quantify the data, we also use a mechanistic fit of the resolved harmonics. We show that all catalysts share the same OER mechanism but require different amounts of activation cycles. We have found three intrinsic properties, which can adequately describe a material for electrocatalysis. First is the activation threshold number (ATN), second is the current normalized to the number of active sites (intrinsic current), and lastly the mass normalized active site density. It was found that Ir on Vulcan has an intrinsic activity at least 3 times higher than the other two materials under consideration, as well as having the highest active site density. From the model fits we can also gain further insight into the mechanistic details for each material. For metallic Ir samples, the rate-limiting step is shown to be water adsorption, whereas for IrO 2 the bottleneck is the inherently slower kinetics. This also indicates that IrO 2 does not produce the same IrOH as Ir metal and therefore has different intrinsic properties. This study provides new insights into the intrinsic properties of different Ir nanocatalysts and highlights a general approach to studying the reaction mechanisms and intrinsic properties of electrocatalysts. [ABSTRACT FROM AUTHOR]