Colloidal synthesis
of nanocrystals (NC) followed by their attachment
to a support and activation is a promising route to prepare model
catalysts for research on structure-performance relationships. Here,
we investigated the suitability of this method to prepare well-defined
Co/TiO2 and Co/SiO2 catalysts for the Fischer–Tropsch
(FT) synthesis with high control over the cobalt particle size. To
this end, Co-NC of 3, 6, 9, and 12 nm with narrow size distributions
were synthesized and attached uniformly on either TiO2 or
SiO2 supports with comparable morphology and Co loadings
of 2–10 wt %. After activation in H2, the FT activity
of the TiO2-supported 6 and 12 nm Co-NC was similar to
that of a Co/TiO2 catalyst prepared by impregnation, showing
that full activation was achieved and relevant catalysts had been
obtained; however, 3 nm Co-NC on TiO2 were less active
than anticipated. Analysis after FT revealed that all Co-NC on TiO2 as well as 3 nm Co-NC on SiO2 had grown to ∼13
nm, while the sizes of the 6 and 9 nm Co-NC on SiO2 had remained stable. It was found that the 3 nm Co-NC on TiO2 already grew to 10 nm during activation in H2.
Furthermore, substantial amounts of Co (up to 60%) migrated from the
Co-NC to the support during activation on TiO2 against
only 15% on SiO2. We showed that the stronger interaction
between cobalt and TiO2 leads to enhanced catalyst restructuring
as compared to SiO2. These findings demonstrate the potential
of the NC-based method to produce relevant model catalysts to investigate
phenomena that could not be studied using conventionally synthesized
catalysts.