Compositional tuning of layered perovskite oxides provides a means of systematically studying how local distortions affect fundamental aspects of electrochemical reaction pathways. Structural analysis of a family of samples La1.2Sr0.8Ni1-yCoyO4 shows that Ni-rich compositions have an expanded crystalline c axis, which is anisotropically compressed by systematic Co incorporation. Raman spectra reveal the strong growth of a symmetry forbidden mode, which suggests that Co acts through localized distortions. Crystallographic and spectroscopic parameters describing this structural distortion correlate to the measured Tafel slopes for the oxygen reduction reaction for all Ni-containing samples, which is attributed to the distortion of potential energy surfaces by the Jahn-Teller expansion of d7 Ni(III) cations. Incorporation of Co not only minimizes the distortion but alters the apparent selectivity of the oxygen reduction reaction away from H2O2 and toward H2O. Rotating ring-disk electrochemical measurements, however, indicate that the apparent change in selectivity is due to activation of a first-order chemical disproportionation of H2O2 that is activated by Co in the lattice. These outcomes will support efforts to design electrocatalysts and reactors for the electrochemical synthesis of H2O2.
Keywords: electrocatalysis; lattice distortions; oxygen reduction reaction; perovskite; peroxide production; reaction mechanism.