ADSORPTION OF H2O ON RU(001) .2. EFFECT OF COADSORBED ALKALI-METALS (NA, K, CS)

被引:35
|
作者
PIRUG, G
RITKE, C
BONZEL, HP
机构
[1] Institut für Grenzflächenforschung und Vakuumphysik, Forschungszentrum Jülich, D-5170 Jülich
关键词
D O I
10.1016/0039-6028(91)90778-Q
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The adsorption of H2O on Na-, K- or Cs-covered Ru(001) is studied at 120-370 K by photoemission spectroscopy and measurements of work-function changes, DELTA-phi. Molecular adsorption at 120 K is prevalent for alkali metal coverages, theta-AM, below a critical coverage which is 0.05, 0.05 and 0.08 for Na, K and Cs, respectively. Changes in DELTA-phi versus H2O adsorption in this alkali metal coverage range are smaller than on the clean surface and become positive for coverages approaching the critical theta-AM. Average dipole moments of H2O, coadsorbed with Na, K and Cs near the critical theta-AM, are approximately 0.2, 0.4 and 0.9 D, respectively. These differences represent a quantitative illustration of the alkali metal specificity of H2O coadsorption. For theta-AM above the critical coverage H2O dissociates into OH and atomic oxygen, with OH being the primary product. The ratio of OH to O is coverage and temperature dependent. H2O dissociation is connected to the finding of tightly adsorbed H2O at 220 K. This species is probably water of hydration of the ionic surface species.
引用
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页码:50 / 62
页数:13
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