MOF-Derived CeO₂ and CeZrO_x Solid Solutions: Exploring Ce Reduction through FTIR and NEXAFS Spectroscopy

The development of Ce-based materials is directly dependent on the catalyst surface defects, which is caused by the calcination steps required to increase structural stability. At the same time, the evaluation of cerium's redox properties under reaction conditions is of increasing relevant importance. The synthesis of Ce-UiO-66 and CeZr-UiO-66 and their subsequent calcination are presented here as a simple and inexpensive approach for achieving homogeneous and stable CeO₂ and CeZrO_x nanocrystals. The resulting materials constitute an ideal case study to thoroughly understand cerium redox properties. The Ce³⁺/Ce⁴⁺ redox properties are investigated by H₂-TPR experiments exploited by in situ FT-IR and Ce M₅-edge AP-NEXAFS spectroscopy. In the latter case, Ce³⁺ formation is quantified using the MCR-ALS protocol. FT-IR is then presented as a high potential/easily accessible technique for extracting valuable information about the cerium oxidation state under operating conditions. The dependence of the OH stretching vibration frequency on temperature and Ce reduction is described, providing a novel tool for qualitative monitoring of surface oxygen vacancy formation. Based on the reported results, the molecular absorption coefficient of the Ce³⁺ characteristic IR transition is tentatively evaluated, thus providing a basis for future Ce³⁺ quantification through FT-IR spectroscopy. Finally, the FT-IR limitations for Ce³⁺ quantification are discussed.