Abstract
AbstractThe local microenvironment at the electrode‐electrolyte interface plays an important role in electrocatalytic performance. Herein, we investigate the effect of acid electrolyte anion identity on the oxygen reduction reaction (ORR) activity and selectivity of smooth Ag and Pd catalyst thin films. Cyclic voltammetry in perchloric, nitric, sulfuric, phosphoric, hydrochloric, and hydrobromic acid, at pH 1, reveals that Ag ORR activity trends as follows: HClO4>HNO3>H2SO4>H3PO4>HCl≫HBr, while Pd ORR activity trends as: HClO4>H2SO4>HNO3>H3PO4>HCl≫HBr. Moreover, rotating‐ring‐disk‐electrode selectivity measurements demonstrate enhanced 4e− selectivity on both Ag and Pd, by up to 35 %H2O2 and 10 %H2O2 respectively, in HNO3 compared to in HClO4. Relating physics‐based modeling and experimental results, we postulate that ORR performance depends greatly on anion‐related phenomena in the double layer, for instance competitive adsorption and non‐covalent interactions.
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