Abstract
The structural evolution of the Ce0.8Gd0.2O1.9 nanocubes supported on Al2O3 and SiO2 was investigated in oxidizing and reducing atmosphere over a temperature range up to 1100°C by XRD, TEM and SEM–EDS methods. The supported Ce0.8Gd0.2O1.9 particles preserved perfect cubic shape to 900°C in oxidizing atmosphere and to 750°C in a hydrogen atmosphere. No evidence of crystalline aluminate or silicate formation was observed for both supports during heating in oxidizing atmosphere up to 1100°C. However, for Ce0.8Gd0.2O1.9/SiO2 segregation of Gd3+ from the mixed oxide and its spreading over the silica surface was noticed at 1000°C–1100°C. Crystalline aluminate/silicate occurred in a hydrogen atmosphere already at 900°C. Apatite type (Ce,Gd)4.67(SiO4)3O mixed silicate was formed after reaction with SiO2 substrate, while monoclinic (Gd,Ce)4Al2O9 and tetragonal (Ce,Gd)AlO3 were formed on Al2O3. The (Gd,Ce)4Al2O9 phase became unstable at 950°C and transformed into (Ce,Gd)AlO3 aluminate, which was stable up to 1100°C. Various mechanisms of the solid-state reaction of mixed ceria with Al2O3 and SiO2 supports operate depending on the size of ceria nanocubes. Small particles (10–30nm) reacted as a whole with the support forming single crystal silicate or aluminate; at the same time, for bigger particles (30–80nm) reactions happen only near the boundary between the particle and the support.
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