CeO2 Modulates the Electronic States of a Palladium Onion-Like Carbon Interface into a Highly Active and Durable Electrocatalyst for Hydrogen Oxidation in Anion-Exchange-Membrane Fuel Cells

This study reports the preparation, characterization, and electro- catalytic properties of palladium-based catalysts containing ceria (CeO2) on carbon black (CB) and onion-like carbon (OLC) supports. The electrocatalysts (Pd-CeO2/CB and Pd-CeO2/OLC) exhibit a large specific surface area, pore volume, and small particle size, as well as enhanced interfacial interaction and synergy among Pd, CeO2, and OLC in Pd-CeO2/OLC that are valuable for improved electrocatalysis. The presence of CeO2 in Pd-CeO2/OLC induces ca. 7% defects and modifies the electronic structure of the Pd/OLC interface, significantly improving the electrical conductivity due to enhanced charge redistribution, corroborated by density functional theory (DFT) calculations. Pd-CeO2/OLC displays the lowest adsorption energies (H*, OH*, and OOH*) among the series. For the hydrogen oxidation reaction (HOR), Pd-CeO2/OLC delivers significantly enhanced HOR (mass-specific) activities of 4.2 (8.1), 13.2 (29.6), and 15 (78.5) times more than Pd-CeO2/CB, Pd/OLC, and Pd/CB, respectively, with the best diffusion coefficient (D) and heterogeneous rate constant (k). Pd-CeO2/OLC also displays less degradation during accelerated durability testing. In an anion-exchange-membrane fuel cell (AEMFC) with H-2 fuel, Pd-CeO2/OLC achieved the highest peak power density of 1.0 W cm(-2) at 3.0 A cm(-2) as compared to Pd-CeO2/CB (0.9 W cm(-2) at 2.2 A cm(-2)), Pd/OLC (0.6 W cm(-2) at 1.7 A cm(-2)), and Pd/CB (0.05 W cm(-2) at 0.1 A cm(-2)). These results indicate that Pd-CeO2/OLC promises to serve as a high-performing and durable anode material for AEMFCs.