Electro-oxidation competency of palladium nanocatalysts over ceria–carbon composite supports during alkaline ethylene glycol oxidation

Direct alcohol fuel cells (DAFCs) are widely regarded as one of the most promising among the futuristic and capable energy systems; direct liquid fuel cells (DLFCs). In this article, we discuss in detail the competency of palladium nanoparticles developed over carbon–ceria composite supports (Pd/C–CeO 2 ) as efficient and durable anode catalysts for the alkaline electro-oxidation of ethylene glycol (EGOR). For the first time, a systematic assessment of the EGOR performance of palladium catalysts with varying Pd–ceria ratios has been reported. The scalable solid-solution route reduction technique enabled the processing of Pd nanoparticles with controlled morphology, size and excellent CeO 2 interaction. The structural features of the prepared catalysts were studied using X-ray diffraction, electron microscopy (TEM) and X-ray photon spectroscopy techniques, while the electrochemical performance of the catalysts was analyzed using cyclic voltammetry and chronoamperometry. During alkaline EGOR, the Pd/C–CeO 2 catalysts showed an enhanced current density (as high as 68.5 mA cm −2 ), more negative onset potential, excellent mass activity (4.6 A mg −1 Pd ) and exceptional durability compared to Pd/C. The enhanced alkaline EGOR kinetics of the Pd/C–CeO 2 catalysts is well attributed to the promotion effect of CeO 2 on Pd by creating more Pd–OH ads and also improved tolerance to poisoning species on the Pd surface. Further, the enhanced ECSA of Pd/C–CeO 2 has also aided the excellent EGOR activity in alkaline medium. The validated enhanced oxidation ability of these Pd/C–CeO 2 catalysts for the anodic oxidation of other low molecular weight alcohol fuels including methanol and ethanol showcased their application potential toward DMFCs and DEFCs.