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submitted on 25.04.2019 and posted on 29.04.2019by Paul Pearce, Chunzhen Yang, Antonella Iadecola, Juan Rodriguez-Carvajal, Gwenaëlle Rousse, Rémi Dedryvère, Artem M. Abakumov, Domitille Giaume, Michael Deschamps, Jean-Marie Tarascon, Alexis Grimaud
We report a strategy to isolate IrO3 as an intermediate for the oxygen evolution reaction (OER). Its reactivity is studied using X-ray absorption spectroscopy, X-ray and neutron diffraction and X-ray photoelectron spectroscopy. Its stability is assessed by using on-line mass spectroscopy and inductively coupled plasma optical emission spectroscopy and presented herein. Upon reaction with water in acidic conditions, we could observe the formation of a new protonated iridate phase of composition H2IrO3. Coupling OER measurements and dissolution rate determination, we could show that its activity and stability are governed by a yet ill-described charge compensation mechanism enlisting reversible bulk proton insertion inside the catalyst structure. This singular property enables an enhanced activity and stability towards dissolution compared to the stellar IrOx/SrIrO3 catalyst. Such a finding opens the route towards the design of new OER catalysts enlisting proton insertion that could be competitive for water splitting in acidic media.