Abstract
Silica-supported ruthenium catalysts prepared from the RuCl3 · 3H2O precursor contain residual chloride after reduction in flowing hydrogen. The amount of this chlorine was determined by X-ray fluorescence spectroscopy to be less than one monolayer on the ruthenium surfaces. Both volumetric hydrogen chemisorption and proton NMR show suppression of hydrogen chemisorption capacity associated with the presence of chlorine contamination, which can be removed effectively with hot water elution. The variations of the hydrogen chemisorption capacity with chlorine coverage suggests that chlorine would completely block and poison the Ru surfaces for hydrogen chemisorption at a Cl coverage of about 76%. The effect of residual chloride on the proton NMR resonance position and the spin-lattice relaxation time for the chemisorbed hydrogen indicates an electronic interaction between Cl adspecies and surface Ru, which results in the weakening of the H-Rus chemisorptive bond at the Ru surfaces. This reduced H-Rus interaction may be the cause for an increase in the ratio of the reversibly adsorbed hydrogen over the irreversibly adsorbed hydrogen with increasing Cl coverage. It is proposed that the mechanism for suppression of hydrogen chemisorption by chlorine involves both physical site blocking of surface Ru atoms and shortranged electronic interactions between Cl adatoms and neighboring surface Ru atoms.
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