Lifecycle of Pd Clusters: Following the Formation and Evolution of Active Pd Clusters on Ceria During CO Oxidation by In Situ/Operando Characterization Techniques

or maximizing the atomic efficiency in noble metal-based catalysts,
dedicated preparation routes and high lifetime are essential. Both aspects require
an in-depth understanding of the fate of noble metal atoms under reaction
conditions. For this purpose, we used a combination of complementary in situ/
operando characterization techniques to follow the lifecycle of the Pd sites in a
0.5% Pd/5% CeO2−Al2O3 catalyst during oxygen-rich CO oxidation. Time-
resolved X-ray absorption spectroscopy showed that Pd cluster formation under
reaction conditions is important for a high CO oxidation activity. In combination
with density functional theory calculations, we concluded that the ideal Pd cluster
size amounts to about 10−30 Pd atoms. The cluster formation and stability were
affected by the applied temperature and reaction conditions. Already short pulses of 1000 ppm CO in the lean reaction feed were
found to trigger sintering of Pd at temperatures below 200 °C, while at higher temperatures oxidation processes prevailed.
Environmental transmission electron microscopy unraveled redispersion at higher temperatures (400−500 °C) in oxygen
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atmosphere, leading to the formation of single sites and thus the loss of activity. However, due to the reductive nature of CO, clusters
formed again upon cooling in reaction atmosphere, thus closing the catalytic cycle. Exploiting the gained knowledge on the lifecycle
of Pd clusters, we systematically investigated the effect of catalyst composition on the cluster formation tendency. As uncovered by
DRIFTS measurements, the Pd to CeO2 ratio seems to be a key descriptor for Pd agglomeration under reaction conditions. While
for higher Pd loadings, the probability of cluster formation increased, a higher CeO2 content leads to the formation of oxidized
dispersed Pd species. According to our results, a Pd:CeO2 weight ratio of 1:10 for CeO2−Al2O3-supported catalysts leads to the
highest CO oxidation activity under lean conditions independent of the applied synthesis method.