In situ diffraction monitoring of nanocrystals structure evolving during catalytic reaction at their surface

Abstract

AbstractWith decreasing size of crystals the number of their surface atoms becomes comparable to the number of bulk atoms and their powder diffraction pattern becomes sensitive to a changing surface structure. On the example of nanocrystalline gold supported on also nanocrystalline $${\text{CeO}}_2$$ CeO 2 we show evolution of (a) the background pattern due to chemisorption phenomena, (b) peak positions due to adsorption on nonstoichiometric $${\text{CeO}}_{2-x}$$ CeO 2 - x particles, (c) Au peaks intensity. The results of the measurements, complemented with mass spectrometry gas analysis, point to (1) a multiply twinned structure of gold, (2) high mobility of Au atoms enabling transport phenomena of Au atoms to the surface of ceria while varying the amount of Au in the crystalline form, and (3) reversible $${\text{CeO}}_2$$ CeO 2 peaks position shifts on exposure to He–X–He where X is O2, H2, CO or CO oxidation reaction mixture, suggesting solely internal alternations of the $${\text{CeO}}_2$$ CeO 2 crystal structure. We found no evidence of ceria lattice oxygen being consumed/supplied at any stage of the process. The work shows possibility of structurally interpreting different contributions to the multi-phase powder diffraction pattern during a complex physico-chemical process, including effects of physi-, chemisorption and surface evolution. It shows a way to structurally interpret heterogeneous catalytic reactions even if no bulk phase transition is involved.