The electrocatalytic behavior of adsorbed lead atoms on mercury towards 0, reduction in neutral electrolyte at ambient temperature is examined. The results show that 0, reduction on these modified surfaces proceeds through the series mechanism and that the enhancement is mainly due to hydrogen perox
On the electrocatalytic properties of ruthenates
โ Scribed by J.A.R. Van Veen; J.M. Van Der Eijk; R. De Ruiter; S. Huizinga
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- English
- Weight
- 669 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0013-4686
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โฆ Synopsis
The reported activity of non-stoichiometric lead and bismuth ruthenates, which have the pyrochlore or a related structure, in the electro-oxidation of olelins is shown not to be due to the ability of these materials to exchange lattice oxygen, ie the oxidation is not initiated by transference of a lattice oxygen atom to the substrate. Rather, activity is found to be associated with the presence of a Ru(V) surface state, capable of being oxidized to Ru(VI) at higher potentials. Alkenes are oxidized by Ru(VI), which is continually regenerated if the potential is kept high enough (heterogeneous redox catalysis). The availability of the Ru(V)/Ru(VI) surface couple is not an exclusive property of the pyrochlore materials-the only condition for its existence seems to be that the parent compound should not be too crystalline. The activity of pyrochlore ruthenates in the electrochemical reduction of dioxygen is only moderate; its mechanism is unclear at present.
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