The development of Pt-free catalyst for anion exchange membrane fuel cells is limited by the sluggish hydrogen oxidation reaction (HOR) at the anode. Previously, the use of CeO2 as a catalyst promoter facilitated drastic ennoblement of Pd for the HOR kinetics in base media. However, further optimization and understanding of the Pd-CeO2 interaction, surface properties, and its influence on HOR are still needed. In this work, three types of Pd-CeO2/C catalysts are synthesized by a flame-based process, where the Pd-CeO2 interface and HOR activity are improved as compared to catalysts prepared by wet-chemistry processes. The correlation between the Pd-CeO2 interaction and HOR activity is established through comparisons with the three types of Pd-CeO2/C synthesized catalysts using electrochemical techniques and X-ray photoelectron spectroscopy.
Cover Letter
Research highlights:Flame-based RSDT process is used to optimize Pd-CeO 2 /C catalyst design.Pd-CeO 2 /C catalysts shows improved Pd-CeO 2 interface.Type 1 and 2 catalyst exhibits higher HOR activity than the state-of-the-art Pd-CeO 2 /C catalysts.
AbstractThe development of Pt-free catalyst for anion exchange membrane fuel cells is limited by the sluggish hydrogen oxidation reaction (HOR) at the anode. Previously, the use of CeO 2 as a catalyst promoter facilitated drastic ennoblement of Pd for the HOR kinetics in base media. However, further optimization and understanding of the Pd-CeO 2 interaction, surface properties, and their influence on HOR are still needed. In this work, three types of Pd-CeO 2 /C catalysts are synthesized by a flame-based process, where the Pd-CeO 2 interface and the HOR activity are improved as compared to catalysts prepared by wetchemistry processes. The correlation between the Pd-CeO 2 interaction and the HOR activity is established through comparisons of three types of Pd-CeO 2 /C synthesized catalysts using electrochemical techniques and X-ray photoelectron spectroscopy.