Abstract
Hollow carbon spheres (HCSs) containing Co nanoparticles placed inside the HCS were synthesized for the first time using polystyrene spheres as a template. The encapsulated Co nanoparticles, after reduction, showed Fischer-Tropsch (FT) activity indicating syngas accessibility through the HCS porous shell. Two Co catalysts promoted by Ru, placed either inside or outside the HCS (CoRu@HCS and Co@HCS@Ru), were also synthesized and characterized. The location of the Co and Ru was confirmed by SEM and TEM analyses. In-situ XRD studies indicated enhanced H2 reduction of the Co oxide to Co, inside the HCS, in the order CoRu@HCS > Co@HCS@Ru > Co@HCS. The CoRu@HCS catalyst had the highest FT activity, and this was ascribed to a primary spillover effect associated with the direct contact of the Co and Ru inside the HCS. A small secondary spillover effect was also noted for Co@HCS@Ru.
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