Electronic Properties and Reactivity of Simulated Fe3+ and Cr3+ Substituted α-Al2O3 (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-Al2O3 (corundum) can contain up to 9.17% (wt./wt.) Fe2O3 and 1.81% (wt./wt.) of Cr2O3. Here the authors report on changes in the structural and electronic properties of undoped and doped α-Al2O3 (0001) surfaces using periodic d. functional theory (DFT) methods with spin unrestricted B3LYP functional and a local at. basis set. Both structural and electronic properties are altered upon doping. Implications for doping effects on photochem. processes are discussed. As metal oxides are major components of the environment, including atm. mineral aerosol, DFT was also used to study the effect of transition metal impurities on gas/surface interactions of a model acidic atm. gas mol., CO. The theor. results indicated that the presence of Fe3+ and Cr3+ 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-Al2O3 when the impurity is substituted below the 1st surface layer. The presence and location of the mineral dopant significantly altered the structural and electronic properties and gas/surface interactions studied here. [on SciFinder(R)]