The electrochemical oxidation of porous lead electrodes is compared and contrasted with that of solid lead. Significant differences between the behaviours of the two electrode types are observed and interpreted in terms of the major component of the oxidation of the porous electrode arising from the
Cyclic voltammetry on lead electrodes in sulphuric acid solution
โ Scribed by W. Visscher
- Publisher
- Elsevier Science
- Year
- 1976
- Tongue
- English
- Weight
- 366 KB
- Volume
- 1
- Category
- Article
- ISSN
- 0378-7753
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โฆ Synopsis
The oxidation of lead in 5 M H2SO4 was studied by cyclic voltammetry. When a potential scan is applied from --1.0 V to 2.6 V vs. R.H.E. the PbSOJPbO2 oxidation peak can be observed in the anodic voltammogram provided the scan rate is 0.16 mV/s or lower. When the potential scan is restricted to the potential range +0.6 V to +2.6 V the anodic voltammogram shows two peaks which were assigned to the formation of ~-PbO2 and /3-PbO 2 respectively. This ~-PbO2 is formed underneath the PbSO4 film. During the reverse sweep the main reduction peak at 1.65 V corresponds with the reduction of ~-PbO2 to PbSO4. ~-PbO2 is not reduced at a definite potential but it is reduced to n-PbO. PbSO4 with n increasing from the oxide-electrolyte interface towards the interior of the electrode and with more cathodic potential. At potentials below 0 V, the basic lead sulphates are reduced.
The effect of the addition of small amounts of H3PO 4 to the H~SO4 electrolyte during the potential scanning results in an increase of the a-PbO2 peak and a disappearance of the ~-PbO2 peak.
๐ SIMILAR VOLUMES
Cyclic voltammetry has been used to study the electrochemical redox behaviour of the Pb/PbO,&PbSO, system on the lead electrode in aqueous H,SO, solutions. The ancdic and the cathodic polarization behaviour has been investigated under the'various conditions by changing the potential region, sweeping
When a fully charged lead negative electrode stood for one month in 1.0 M H,SO, solution at a temperature of 298.15K, it was passivated through so-called "sulfation" as indicated by a decrease in the redox peak currents on cyclic voltammograms. As a method of reactivating the passivated lead negati
There are wide discrepancies in the reported current density values (ti p and i0,~) obtained from potentiodynamic studies on lead in sulphuric acid solutions . Furthermore, it is well known that preparative procedures exert a marked influence on the data obtained for planar electrodes. The present i