A DFT study of the adsorption and dissociation of CO on sulfur-precovered Fe100

Sulfur is known to be a poison to several catalytic reactions, e.g., the Fischer-Tropsch synthesis (FTS), in which it affects drastically the performance of both iron- and cobalt-based catalysts. However, despite the importance of this industrial process, little is known about what elementary steps are poisoned by sulfur. In the present article, we report, using density functional theory, the effect of sulfur on one of the most relevant reactions in the FTS: the dissociation of carbon monoxide over iron surfaces. We have studied the adsorption and dissociation of CO on Fe(100)-S-p(2 x 2) (theta(S) = 0.25 ML) and on Fe(100)-S-c(2 x 2) (theta(S) = 0.50 ML). We have found surface configurations that correlate well with the desorption features observed in temperature-programmed desorption mass spectroscopy. In addition, we have calculated the activation energy of CO dissociation on Fe(100)-S-p(2 x 2), which, interestingly, is very similar to the activation energy of CO dissociation on the sulfur-free Fe(100) surface. However, the sign of the reaction changes by the presence of sulfur; CO dissociation is highly exothermic on the sulfur-free Fe(100) surface, whereas on the Fe(100)-S-p(2 x 2) surface, it is slightly endothermic. Moreover, according to our results, the influence of sulfur in the CO dissociation seems to be short-ranged.