Abstract
An attempt has been made to analyze the spin quenching properties of Mn, as a representative of transition metals, in Mn·MgO, Mn·CaO, OC·Mn·MgO, and OC·Mn·CaO complexes formed at the regular (001) surfaces of MgO and CaO, as well as the adsorption of CO on Mn deposited on MgO and CaO by means of hybrid density functional theory calculations and embedded cluster model. Clusters of moderate sizes were embedded in the simulated Coulomb fields that closely approximate the Madelung fields of the host surfaces. A test has been made to examine the effect of artificial flow of charge. While the spin states of Mn in Mn·MgO and Mn·CaO complexes are preserved, the combined effects of adsorbate and substrate in OC·Mn·MgO and OC·Mn·CaO complexes are strong enough to favor the low spin states and to quench the spin. The deposited Mn atoms enhance the adsorption of CO on MgO and CaO surfaces. The significant weakening of bond strength between OC and Mn in complexes supports the concept of bond order conservation. The relation between the strength of CO adsorption and the basicity of the support is verified. The natural bond orbital analysis reveals that the electronic structure of the adsorbed metal represents a qualitative change with respect to that of the free metal. The effects of spin contamination on the geometry, Mulliken charges, and adsorption energy are examined. The binding of CO precursor is dominated by the E(i)Mn···CO pairwise additive components in MgO and CaO complexs, and the role of the support is not restricted to supporting the metal. The adsorbed CO molecules exhibit no remarkable deviation from linearity. Finally, relations are established between the process of spin quenching and the energy gaps between frontier orbitals. The results show that the spin state of adsorbed metal atoms on oxide supports and the role of precursor molecules on the magnetic and binding properties of complexes need to be explicitly taken into account. © 2012 Wiley Periodicals, Inc.
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