CeO2 promotes electrocatalytic formic acid oxidation of Pd-based alloys

Engineering metal/oxide interface and controlling composition are the important strategies that aim towards obtaining efficient Pd-based electrocatalysts (ECs). Rationally designed ECs for dehydrogenation of formic acid play a dynamic role in the proper utilization of its chemical energy. Herein, we report Pd3M alloy nano-particles anchored on C-CeO2 (Pd3M/C-CeO2, M = Cu, Ni, Co) which shows significant performance towards formic acid oxidation (FAO). Interestingly, Pd3M/C-CeO2 (M = Cu, Ni, Co) ECs displayed the best FAO activity via the dehydrogenation pathway. The remarkable performance can be mainly attributed to the proper electronic and synergistic effects between Pd and the alloyed metal, which leads to Pd lattice contraction and downshift of d-band center. It was also observed that the FAO activity of Pd3Cu/C-CeO2 is superior to that of Pd3Co/C-CeO2 and Pd3Ni/C-CeO2. The oxygen vacancies in CeO2 and strong Pd/CeO2 interactions established by computational and experimental studies contribute towards the overall electrocatalytic behaviour.2023 Elsevier B.V. All rights reserved.

Automated summary

Engineering metal/oxide interface and controlling composition are important strategies for efficient Pd-based electrocatalysts. In this study, Pd3M alloy nano-particles anchored on C-CeO2 (Pd3M/C-CeO2, M = Cu, Ni, Co) demonstrated significant performance in formic acid oxidation. The improved activity can be attributed to the electronic and synergistic effects between Pd and the alloyed metal, resulting in lattice contraction and downshift of d-band center. The presence of oxygen vacancies in CeO2 and strong Pd/CeO2 interactions also contribute to the overall electrocatalytic behavior.