These findings can be explained by different binding energies of oxygenated species on the surface of IrOx and RuOx. Simulated XAS spectra show that the average Ir oxidation state change is strongly affected by the coverage of atomic O. The observed shifts in oxidation state suggest that the surface has a high coverage of O at potentials just below the potential where oxygen evolution is exergonic in free energy. This observation is consistent with the notion that the metal–oxygen bond is stronger than ideal.
Anders F. Pedersen, Mria Escudero-Escribano, Bela Sebök, Anders Bodin, Elisa Paoli, Rasmus Frydendal, Daniel Friebel, Ifan E. L. Stephens, Jan Rossmeisl, Ib Chorkendorff and Anders Nilsson
J. Phys. Chem. B, Oct. 2017
DOI: 10.1021/acs.jpcb.7b06982
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