Ahstract ~ The mechanism for the anodic formation of peroxydisulfate ion on a Ti-supported IrO, electrode was investigated in mixed aqueous solutions of H,SO., (NH&SO4 and NH,F. Peroxydisulfate ion can be formed in higher yield at lower overpotential on the Ti-supported IrO, electrode. comoared with
Kinetics and mechanism of oxygen evolution on IrO2-based electrodes containing Ti and Ce acidic solutions
โ Scribed by V.A. Alves; L.A. da Silva; J.F.C. Boodts; S. Trasatti
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 531 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0013-4686
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โฆ Synopsis
Abstrati-A systematic investigation of the mechanistic features, the electrocatalytic activity, and the stability of thermally prepared ternary oxides of general formula Ir, ,,Ti,,,,_,,Ce,O, (0 d x C 0.7) has been carried out using 0, evolution from 1.0 mol dm-3 aqueous HCIO, as a model reaction. The surface state of the electrodes was monitored in situ by recording voltammetric curves before and after each experiment. Stability was tested by cycling the electrodes between 0.4 and 1.4V @he). For all compositions the anodic-to-cathodic charge ratio, qJqe, was close to one. Variation of the negative potential limit did not reveal the occurrence of the cathodic dissolution phenomena previously observed with a similar RuO,-based system. Tafel slopes were independent of the CeO, content, with a value around 30mV. The reaction order with respect to H+ was zero at constant overpotential and ionic strength. Some inhibition of the oxygen evolution reaction is observed as Ti is replaced by Ce.
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