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The oxidation of CO on RuO2(110) at room temperature

MPS-Authors
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Fan,  Chao Yang
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Wang,  Jinhai
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Jacobi,  Karl
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Ertl,  Gerhard
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Citation

Fan, C. Y., Wang, J., Jacobi, K., & Ertl, G. (2001). The oxidation of CO on RuO2(110) at room temperature. The Journal of Chemical Physics, 114(22), 10058-10062. doi:10.1063/1.1350817.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0011-1825-1
Abstract
RuO2(110) surfaces were prepared by exposing Ru(0001) to 10(7) L of O-2 at 700 K. Postexposure of O-2 at 300 K resulted in an additional oxygen species (O-cus) adsorbed on coordinatively unsaturated Ru atoms (Ru-cus). The surface was then exposed to CO at 300 K and studied by thermal desorption spectroscopy (TDS) and high-resolution electron energy loss spectroscopy (HREELS). It is demonstrated that CO is oxidized at 300 K through reaction with both the O-cus as well as with surface O-atoms held in bridge positions (O-bridge). Although-at room temperature-CO adsorbs intermediately on the Ru-cus atoms, it is stable only at the Ru atoms underneath the O-bridge after the latter has been reacted off. At room temperature only surface oxygen takes part in the CO oxidation and the oxygen-depleted surface can be restored by O-2 exposure, so that under steady-state flow conditions an oxygen-deficient surface will exist whose stoichiometry will be determined by the ratio of partial pressures.