Abstn~ct--Anodic and catalytic oxidations of formate ion at an active Pd electrode were studied by the potential-sweep and the galvanostatic methods in connexion with the measurements of the rate of formation of hydrogen on Pd during the catalytic decomposition of formate. A Pd surface oxidized by p
Specular reflectivity studies of the adsorption and the oxidation of methanol on palladium in an alkaline solution
β Scribed by Tsutomu Takamura; Yuichi Sato
- Publisher
- Elsevier Science
- Year
- 1974
- Tongue
- English
- Weight
- 568 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0013-4686
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β¦ Synopsis
Adsorption and anodic oxidation of methanol on palladium electrode in Q5 N NaOH was studied by measuring current-potential (i-E) and reflectivity-potential
curves. Presence of methanol retarded the formation of the oxide layer of Pd, giving rise to an anodic shift of the potential. A linear relation was found between the potential retarded and the logarithm of methanol concentration, the slope being about 30 mV/decade. The form of adsorbed entities was discussed based on the slope. The cathodic charge consumed by the reduction of Pd-oxide was smaller in the presence of methanol than in the absence. This was explained by three causes; the less amount of oxide layer formed during the anodic sweep owing to the adsorption of oxidation product of methanol, the reduction of formed oxide layer by a chemical reaction with methanol, and a compensation effect due to the anodic oxidation of methanol during the cathodic sweep. Plottings of the total charge in the anodic region US -AR/R,, in the absence and the presence of methanol suggested that electro-oxidation of methanol proceeds only at the bare portion of Pd.
π SIMILAR VOLUMES
Periodic current/potential curves were measured potentiostatically on smooth electrodes of platinum, iridium, rhodium, and gold at 30 mV/s in perchloric acid solutions with different additions of methanol (10e3 M to 1 M). Information on methanol adsorption was obtained from impedance measurements at