Modulating CO hydrogenation activity through silane functionalization of cobalt catalysts

Abstract

Cobalt oxide (CoO) nanoparticles (NPs) were modified with different silanes (tetraethoxysilane – TEOS, triphenyl ethoxysilane – TPES, or trimethyl chlorosilane - TMCS) by dispersing the as-synthesized CoO NPs in n-hexane solutions containing the silanes. Fourier-transform infrared spectroscopy (FTIR) confirmed the presence of these silanes on the cobalt surfaces even after reduction in hydrogen (H2) at 573 K. Modifying CoO-NPs with TEOS resulted in face-centred cubic (fcc)-cobalt phase upon reduction whereas TPES or TMCS modification induced a mixture of hexagonal close-packed (hcp)- and fcc-cobalt phases. The modification of cobalt surfaces with the silanes alters the adsorption properties of carbon monoxide (CO) on the catalytically active sites. Furthermore, temperature programmed desorption of CO (CO-TPD) showed that the amount of dissociatively adsorbed CO relative to amount of associatively adsorbed CO increases on silane-modified cobalt surfaces, which correlates with an improved rate of CO conversion in the Fischer-Tropsch CO hydrogenation.