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Polyoxometalate grafting onto silica: stability diagrams of H₃PMo₁₂O₄₀ on {001}, {101}, and {111} β-cristobalite surfaces analyzed by DFT

Xavier Rozanska, P Sautet, F Delbecq, F Lefebvre, S Borshch, H Chermette, J Basset, and E Grinenval
Physical Chemistry Chemical Physics 13, no. 35 (2011): 15955.

The process of grafting H₃PMo₁₂O₄₀ onto silica surfaces is studied using periodic density functional theory methods. For surfaces with a high hydroxyl coverage, the hydroxyl groups are consumed by the polyoxometalate protons, resulting in water formation and the creation of a covalent bond between the polyoxometalate and the surface, and mostly no remaining acidic proton on the polyoxometalate. When the surfaces are partially dehydroxylated and more hydrophobic, after temperature pretreatment, less covalent and hydrogen bonds are formed and the polyoxometalate tends to retain surface hydroxyl groups, while at least one acidic proton remains. Hence the hydroxylation of the surface has a great impact on the chemical properties of the grafted polyoxometalate. In return, the polyoxometalate species affects the compared stability of the partially hydroxylated silica surfaces in comparison with the bare silica case.