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Interaction of CO with the stoichiometric RuO2(110) surface

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Kim,  Sang Hoon
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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Paulus,  Ursula A.
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

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

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Wintterlin,  Joost
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

Kim, S. H., Paulus, U. A., Wang, Y., Wintterlin, J., Jacobi, K., & Ertl, G. (2003). Interaction of CO with the stoichiometric RuO2(110) surface. Journal of Chemical Physics, 119(18), 9729-9736. doi:10.1063/1.1614205.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0011-0ED1-E
Abstract
The adsorption of CO on RuO2(110) single-crystalline thin films grown on Ru(0001) was studied with scanning tunneling microscopy (STM), thermal desorption spectroscopy (TDS), and high-resolution electron energy-loss spectroscopy. The stoichiometric RuO2(110) surface exhibits alternating rows of O-bridge and coordinatively unsaturated Ru atoms (Ru-cus). We identify two different CO adsorption states: CO-bridge and CO-cus. CO-bridge is known to adsorb at the O-bridge positions after reacting-off O-bridge. CO-cus is linearly bonded to Ru-cus in an on-top position and becomes stabilized only after complete filling of the CO-bridge sites. The CO-cus state exhibits two desorption maxima, at 200 and 320 K, corresponding to a surface coverage of approximately 1.0 (alpha state) and 0.5 (beta state), respectively. At 300 K and without CO gas in the background, CO-cus remains only temporarily present at the surface, and reaches coverages of 0.5. A coverage of 1.0 can be achieved by exposure to CO at 300 K to prepare CO-bridge and further exposure to CO at 85 K. From time-dependent STM and from TDS the binding energy of the beta-state CO-cus is determined at about –1.0 eV.