Electronic properties and reactivity of simulated Fe(3+) and Cr(3+) substituted α-Al(2)O(3) (0001) surface

Metal oxide based minerals naturally contain transition metal impurities isomorphically substituted into the structure that can alter the structural and electronic properties as well as the reactivity of these metal oxides. Natural α-Al(2)O(3) (corundum) can contain up to 9.17% (w/w) Fe(2)O(3) and 1.81% (w/w) of Cr(2)O(3.) Here we report on changes in the structural and electronic properties of undoped and doped α-Al(2)O(3) (0001) surfaces using periodic density functional theory (DFT) methods with spin unrestricted B3LYP functional and a local atomic basis set. Both structural and electronic properties are altered upon doping. Implications for doping effects on photochemical processes are discussed.As metal oxides are major components of the environment, including atmospheric mineral aerosol, DFT was also used to study the effect of transition metal impurities on gas/surface interactions of a model acidic atmospheric gas molecule, carbon monoxide (CO). The theoretical results indicated that the presence of Fe(3+) and Cr(3+) impurities substituted on the outer layer of natural corundum surfaces reduces the propensity toward CO adsorption relative to the undoped surface. However, CO-surface interactions resemble that of bulk α-Al(2)O(3) when the impurity is substituted below the first surface layer. The presence and location of the mineral dopant was found to significantly alter the structural and electronic properties and gas/surface interactions studied here.