An in situ study of the NO + H2 + O2 reaction on Pd/LaCoO3 based catalysts

In situ X-ray diffraction (XRD) and quasi in situ X-ray photoelectron spectroscopy (XPS) measurements were complementary used to investigate structural and surface modifications of a palladium-supported on LaCoO3 perovskite catalyst under various controlled atmospheres, particularly during the reduction of NO by hydrogen under lean conditions, in the presence of a large excess of oxygen. An extensive reduction of the perovskite was evidenced during the pre-activation thermal treatment of the palladium-supported catalyst under hydrogen at 773 K leading to the formation of Pd particles in contact with Co0 and La2O3. In the presence of an excess of oxygen, the catalyst structure changes during the reaction. The reduced solid is progressively transformed into LaCoO3 in the range of 873–1173 K. However, such a bulk transformation probably occurs at lower temperatures at the surface of the solid according to XPS analyses. At the same time, the binding energy (BE) level of the Pd 3d5/2 photopeak increases up to 337.5 eV which reveals the stabilisation of oxidic palladium species in a different chemical environment than that corresponding to PdO. Such changes induced different catalytic properties of the catalyst during the reduction of NO by H2.