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Interaction of dioxygen with the platinum Pt19/SnO2/H2 cluster: DFT calculation

  • Theoretical Inorganic Chemistry
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Abstract

The adsorption of the O2 molecule onto the surface of the Pt19 platinum cluster deposited onto the tin dioxide crystal surface in the presence of dissociated hydrogen molecule has been calculated by the density functional theory method within the generalized gradient approximation (GGA-PBE) with periodic boundary conditions and a projector-augmented plane-wave (PAW) basis set. It has been demonstrated that the oxygen molecule can be adsorbed without a barrier onto the free surface of the Pt19/SnO2/H2 cluster to form a superoxy isomer with one Pt-O bond (the energy of elimination of the oxygen molecule is 0.75 eV), which converts almost without a barrier to more stable peroxide isomers with two Pt-O bonds (the energy of elimination of the O2 molecule is 1.2−1.7 eV). The energy of elimination of the oxygen molecule from the isomers with two-coordinated oxygen positions at the cluster edges is 2.10−2.53 eV. The isomers with mono- and tricoordinated oxygen positions are less energetically favorable than the isomers with two-coordinated oxygen positions. The process of addition of the oxygen molecule to the platinum cluster and elimination of the water molecule formed in the reaction Pt19/SnO2/H2 + O2 → Pt19/SnO2/O + H2O is energetically favorable by 1.6 eV.

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Authors and Affiliations

  1. Institute of Problems of Chemical Physics, Russian Academy of Sciences, Chernogolovka, Moscow oblast, 142432, Russia

    T. S. Zyubina, A. S. Zyubin, Yu. A. Dobrovol’skii & V. M. Volokhov

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  1. T. S. Zyubina
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  2. A. S. Zyubin
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  3. Yu. A. Dobrovol’skii
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  4. V. M. Volokhov
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Original Russian Text © T.S. Zyubina, A.S. Zyubin, Yu.A. Dobrovol’skii, V.M. Volokhov, 2013, published in Zhurnal Neorganicheskoi Khimii, 2013, Vol. 58, No. 3, pp. 360–369.

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Zyubina, T.S., Zyubin, A.S., Dobrovol’skii, Y.A. et al. Interaction of dioxygen with the platinum Pt19/SnO2/H2 cluster: DFT calculation. Russ. J. Inorg. Chem. 58, 311–319 (2013). https://doi.org/10.1134/S0036023612120236

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