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Electrochemical hydration and reaction processes on metal surfaces studied by gas phase adsorption

MPG-Autoren
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Sass,  Jürgen-Kurt
Fritz Haber Institute, Max Planck Society;

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Lackey,  Damian
Fritz Haber Institute, Max Planck Society;

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Schott,  Joachim
Fritz Haber Institute, Max Planck Society;

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Zitation

Sass, J.-K., Lackey, D., & Schott, J. (1991). Electrochemical hydration and reaction processes on metal surfaces studied by gas phase adsorption. Electrochimica Acta, 36(11-12), 1883-1887. doi:10.1016/0013-4686(91)85062-C.


Zitierlink: https://hdl.handle.net/21.11116/0000-0009-F113-1
Zusammenfassung
The distinction between surface hydration and reaction processes in ultrahigh vacuum studies of electrochemical phenomena is illustrated by coadsorption of H2O with: (i) Cs on Cu(110); at low caesium coverages, solvation of the adsorbed alkali is observed and above a critical coverage of θCs = 0.15 a surface reaction occurs forming hydroxide and hydrogen. Work function measurements have also been used to characterize the dielectric screening by interfacial water; (ii) hydrogen on Cu(110) and Pt(111): TDS and HREELS measurements using isotopic substitution of hydrogen by deuterium have been used to investigate the formation of (H3O+)ad. Whereas on Cu(110) hydrogen is merely solvated by water, on Pt(111) there is evidence for the production of hydrated protons.