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Preparation of Cobalt Nanocrystals Supported on Metal Oxides To Study Particle Growth in Fischer–Tropsch Catalysts

[Image: see text] 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/TiO...

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Detalles Bibliográficos
Autores principales: van Deelen, Tom W., Nijhuis, Jelle J., Krans, Nynke A., Zečević, Jovana, de Jong, Krijn P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219851/
https://www.ncbi.nlm.nih.gov/pubmed/30416841
http://dx.doi.org/10.1021/acscatal.8b03094
Descripción
Sumario:[Image: see text] 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/TiO(2) and Co/SiO(2) 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 TiO(2) or SiO(2) supports with comparable morphology and Co loadings of 2–10 wt %. After activation in H(2), the FT activity of the TiO(2)-supported 6 and 12 nm Co-NC was similar to that of a Co/TiO(2) catalyst prepared by impregnation, showing that full activation was achieved and relevant catalysts had been obtained; however, 3 nm Co-NC on TiO(2) were less active than anticipated. Analysis after FT revealed that all Co-NC on TiO(2) as well as 3 nm Co-NC on SiO(2) had grown to ∼13 nm, while the sizes of the 6 and 9 nm Co-NC on SiO(2) had remained stable. It was found that the 3 nm Co-NC on TiO(2) already grew to 10 nm during activation in H(2). Furthermore, substantial amounts of Co (up to 60%) migrated from the Co-NC to the support during activation on TiO(2) against only 15% on SiO(2). We showed that the stronger interaction between cobalt and TiO(2) leads to enhanced catalyst restructuring as compared to SiO(2). 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.