Redox Mechanisms of Silica-Supported Ni Particles: An X-Ray Absorption Fine Structure Investigation

The redox mechanisms of silica-supported Ni particles were investigated using their in situ X-ray absorption fine structure, providing mechanistic insights into partially reduced NiO and partially oxidized metallic Ni. The results of surface oxidation of partially reduced NiO particles at room temperature revealed that the surface was not fully covered with metallic Ni and that metallic Ni had also formed within the particle interior. During NiO particle reduction, the process initiates at specific surface sites, and before the metallic Ni phase fully covers the surface, O2− ions are expelled from the particle. Conversely, the oxidation of metallic Ni particles progresses inward from the surface, with an accompanying increase in the thickness of the NiO layer that forms upon O2 exposure at room temperature. This mechanism is supported by observations that the reduction of a thin NiO shell on metallic Ni particles was completed below 200 °C, while reduction temperatures shifted to higher values as the NiO layer thickness increased. The distinct oxidation and reduction mechanisms are attributed to differences in the migration direction of O2− ions. During reduction, it is proposed that O2− ions within the particles migrate to the surface along the interface between the NiO phase and the metallic Ni phase. This study elucidates the detailed mechanism behind the redox interconversion between NiO and metallic Ni in solid catalyst particles.