Long-Range Oxygen Spillover at the Cu/CeO2 Interface

Reverse oxygen spillover (ROS) from ceria (CeO ₂ ) to supported metal species, driven by strong metal-support interactions, profoundly impacts not only their catalytic efficacy but also the structural stability, dispersion, and electronic characteristics of the metal active sites. Herein, we for the first time observed a long-range dynamic ROS phenomenon at the interface of Cu/CeO ₂ catalysts by means of first-principle calculations, ab-initio and deep-potential molecular dynamics (DPMD) simulations. The ROS process is initiated by interfacial lattice oxygen transfer to Cu species, followed by sequential migration of adjacent O atoms via oxygen vacancies, resulting in progressive oxidation of supported Cu species. In addition, DPMD simulations reveal the persistence of the long-range ROS process over larger time and spatial scales, with larger Cu NPs exhibiting faster and more extensive ROS. These findings provide mechanistic insights into the importance of long-range ROS behaviors in the preparation of oxide-supported metal catalysts.