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Iridium oxides are common oxygen evolution catalysts, combining high activity with decent stability. However, these properties vary strongly with the IrO x  form, ranging from durable crystalline IrO 2  to more active but less stable amorphous, hydrous oxides. Herein we demonstrate how an operation transient during proton exchange membrane water electrolysis (PEMWE) can induce conversion of IrO 2  in the anode catalyst layer into a more hydrous form. We operate a 5 cm 2  PEMWE cell at 80 °C and elevated H 2  pressure, then interrupt the power supply and observe the OCV showing a characteristic decay to eventually 0 V. We postulate that the IrO 2  surface reacts with H 2  crossing over the membrane, confirm ex situ via TGA and XRD analyses that IrO x  can be reduced to metallic Ir under H 2  at 80 °C, elaborate the related thermodynamics and match them with the electrochemical potential of the IrO x  catalyst during the above transient. This is supported in situ via cyclic voltammograms and polarization curves showing improved OER activity. Moreover, we demonstrate that subsequent polarization to the OER potential range transforms the reduced catalyst surface into a more hydrous IrO x  and wrap up with implications for the long-term performance and durability of PEMWE devices.

Transformation of the OER-Active IrOxSpecies under Transient Operation Conditions in PEM Water Electrolysis

Transformation of the OER-Active IrO_xSpecies under Transient Operation Conditions in PEM Water Electrolysis