The development of catalyst for the oxidation of water that operates at PH 7, 1 atm, and room temperature is a fundamental chemical challenge. As a all-inorganic catalyst for the rapid oxidation of water to dioxygen working in aqueous solution at PH 7, ruthenium-containing polyoxometalate (POM), [{Ru 4O4(OH)2(H2O)4}(γ- SiW10O36)2]10-, have been reported by two research groups, respectively. But the details of this mechanism are still lacking. A description of the electronic structure and demonstration of redox tenability of this catalyst are herein provided by means of density functional theory (DFT) calculations. The results show that [Ru 4O4(OH)2(H2O)4] core in this POM is the withdrawing electron group, the FMO of this POM delocalizes over the [Ru4(μ-O)4(μ-OH)2] core, which indicate that ruthenium and oxygen atoms are the redox centers. The role of POM ligand in this catalyst has been evaluated according to our DFT calculations; the results show that it is the key structural factor in determination of stability for this catalyst. The POM ligand's effect significantly changes the redox properties of these clusters. A linear dependence between the one-electron-oxidized energy and the anion charge is found, with a slope of average 0.21 V per two unit charges for tungstates, and 0.13 V per two unit charges for molybdates. The first oxidization step becomes more difficult as substitution of POM ligands (X=Al, Si, P, S). For the same total charge of clusters in tungstates and molybdates, the first oxidization step of tungstates becomes more favorable compared with molybdates. © 2011 Springer-Verlag Berlin Heidelberg.
CITATION STYLE
Sun, M. J., Lin, Y. H., Wang, P., Hu, Q., & Wang, Y. Q. (2011). Quantum chemical studies on all-inorganic catalyst for the oxidation of water to dioxygen ([{Ru4O4(OH)2(H 2O)4}(γ-SiW10O36) 2]10-): Electronic property and redox tunability. In Communications in Computer and Information Science (Vol. 211 CCIS, pp. 487–494). https://doi.org/10.1007/978-3-642-23062-2_73
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