Interface dynamics of Pd-CeO2 single-atom catalysts during CO oxidation

In recent years, noble metals atomically dispersed on solid oxide supports have become a frontier of heterogeneous catalysis. In pursuit of an ultimate atom efficiency, the stability of single-atom catalysts is pivotal. Here we compare two Pd/CeO2 single-atom catalysts that are active in low-temperature CO oxidation and display drastically different structural dynamics under the reaction conditions. These catalysts were obtained by conventional impregnation on hydrothermally synthesized CeO2 and one-step flame spray pyrolysis. The oxidized Pd atoms in the impregnated catalyst were prone to reduction and sintering during CO oxidation, whereas they remained intact on the surface of the Pd-doped CeO2 derived by flame spray pyrolysis. A detailed in situ characterization linked the stability of the Pd single atoms to the reducibility of the Pd-CeO2 interface and the extent of reverse oxygen spillover. To understand the chemical phenomena that underlie the metal-support interactions is crucial to the rational design of stable single-atom catalysts.

Automated summary

In this study, two Pd/CeO2 single-atom catalysts for low-temperature CO oxidation were compared, revealing the impact of preparation method on their stability. Detailed in situ characterization linked the stability of the Pd single atoms to the properties of the Pd-CeO2 interface. Understanding such metal-support interactions is crucial for the rational design of stable single-atom catalysts.