Experimental and theoretical study of the reactions between small neutral iron oxide clusters and carbon monoxide.

Reactions of small neutral iron oxide clusters (FeO(1-3) and Fe(2)O(4,5)) with carbon monoxide (CO) are investigated by experiments and first-principle calculations. The iron oxide clusters are generated by reaction of laser-ablation-generated iron plasma with O(2) in a supersonic expansion and are reacted with carbon monoxide in a fast flow reactor. Detection of the neutral clusters is through ionization with vacuum UV laser (118 nm) radiation and time-of-flight mass spectrometry. The FeO(2) and FeO(3) neutral clusters are reactive toward CO, whereas Fe(2)O(4), Fe(2)O(5), and possibly FeO are not reactive. A higher reactivity for FeO(2) [sigma(FeO(2) + CO) > 3 x 10(-17) cm(2)] than for FeO(3) [sigma(FeO(3) + CO) approximately 1 x 10(-17) cm(2)] is observed. Density functional theory (DFT) calculations are carried out to interpret the experimental observations and to generate the reaction mechanisms. The reaction pathways with negative or very small overall barriers are identified for CO oxidation by FeO(2) and FeO(3). The lower reactivity of FeO(3) with respect to FeO(2) may be related to a spin inversion process present in the reaction of FeO(3) with CO. Significant reaction barriers are calculated for the reactions of FeO and Fe(2)O(4-5) with CO. The DFT results are in good agreement with experimental observations. Molecular-level reaction mechanisms for CO oxidation by O(2), facilitated by condensed phase iron oxides as catalysts, are suggested.