Facile dissociation of CO on Fe{211}: Evidence from microcalorimetry and first-principles theory

作者：Borthwick David; Fiorin Vittorio; Jenkins Stephen J; King David A^*

来源：Surface Science, 2008, 602(13): 2325-2332.

DOI：10.1016/j.susc.2008.05.014

• density functional calculations
• single-crystal adsorption calorimetry
• sticking
• heat of adsorption
• carbon monoxide
• stepped iron surfaces

Chemisorption of CO on the Fe{211} surface is studied within first-principles density functional theory (DFT) and single-crystal adsorption calorimetry (SCAC). The most stable molecular adsorption state corresponds to CO bound in a three-fold site involving one metal atom from the top layer and two metal atoms in the second layer. In this configuration, CO is tilted and elongated with a considerably red-shifted stretching frequency (calculated to be 1634 cm(-1) as opposed to 2143 cm(-1) for gas-phase CO). This state is very similar to that of CO on Fe{100} and Fe{111}, which is believed to be a precursor state to dissociation at relatively modest temperatures. However, dissociation of CO is found by DFT to be particularly facile on Fe{211}, with a dissociation barrier noticeably lower than that for CO on Fe{100} or Fe{111}. The 300 K coverage-dependent calorimetric data is consistent with either molecular or dissociative adsorption, with an initial adsorption heat of 160 kj/mol. At higher coverages, the heat of adsorption and sticking probability data exhibit a forced oscillatory behaviour, which can be explained by assuming CO dissociation and subsequent diffusion of atomic carbon and/or oxygen into the substrate. it is argued that conditions for CO dissociation on Fe{211} are nearly optimal for Fischer-Tropsch catalysis. 2008 Elsevier B.V.

• 出版日期2008-7-1