Adsorption of CO on Ru and Pt blacks and catalysts and the possibility of its utilization for the determination of the ruthenium-free surface |
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Authors: | Ivo Paseka |
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Affiliation: | (1) Institute of Inorganic Chemistry, Academy of Sciences of the Czech Republic, 250 68 Rez, Czech Republic |
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Abstract: | Electrochemical voltammetric curves on Ru and Pt blacks of a different surface area were measured in potential intervals 0.05–1.05 V
in pure 0.5 M H2SO4 and after CO adsorption. It was proved that after the CO adsorption, the outset of ruthenium oxidation is shifted by about
150 mV towards the positive potentials, e.g. to the region of oxidation of adsorbed CO. This fact made possible the determination
of a double-layer charging current of Ru electrodes and, subsequently, also the determination of the amount of adsorbed hydrogen
on the Ru surface. An evaluation of the amount of CO and hydrogen adsorption showed that the ratio of adsorbed CO:H on the
Pt surface was about 1:1, while on Ru electrodes this ratio was around twice as large. The amount of hydrogen adsorbed on
Ru blacks depends on the preliminary preparation of the electrodes. The CO adsorption could also be employed in the determination
of a charging current of electrode double-layers during voltammetric oxidation of adsorbed hydrogen on ruthenium supported
on Al2O3, SiO2, or TiO2 carriers. However, a similar determination of hydrogen adsorbed on the tin-modified Ru catalysts is not very reliable. |
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Keywords: | Hydrogen/carbon monoxide adsorption Platinum/ruthenium catalysts Specific surface |
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