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Rotating ring-disk studies of oxidized nickel hydrous oxide: oxygen evolution and pseudocapacitance
- Source :
- Journal of Electroanalytical Chemistry. 468:64-69
- Publication Year :
- 1999
- Publisher :
- Elsevier BV, 1999.
-
Abstract
- A rotating ring-disk electrode (RRDE) method is herein described for studies of O 2 evolution on nickel hydrous oxide films, NiO x (hydr.), electrodeposited on the gold disk of a Au–Au RRDE in aqueous 1.0 M KOH. This technique relies on the quantitative detection of O 2 generated at the NiO x (hydr.) ∣ Au disk electrode during a linear potential scan, by the concentric, bare Au-ring electrode, which can then be used to determine contributions to the disk current ( I disk ) derived solely from O 2 evolution. Subtraction of such contributions from I disk in the potential range positive to the trailing edge of the peak ascribed to the oxidation of the NiO x (hydr.) film revealed a constant, positive current when the voltage was scanned in the positive direction, and a constant, negative current, albeit of smaller magnitude, in the subsequent scan in the negative direction. This observation suggests that once account is made for O 2 evolution, the NiO x (hydr.) ∣ Au-electrolyte interface in that potential range (0.5–0.65 V vs. Hg ∣ HgO,OH − ), behaves as a (pseudo) capacitor, a model that was further confirmed by monitoring the current as a function of the scan rate. The actual values of this pseudocapacitance were found to be on the order of ca. 80 kF mol −1 Ni sites in the film (or equivalently, ca. 0.1 e − per Ni site within the potential range specified above) and, thus, very similar to those reported earlier based on current interruption-potential decay and impedance measurements for O 2 evolution on NiO x (hydr.) grown on Ni electrodes. Implications of these results to the mechanism of self-discharge of NiO x (hydr.) electrodes for alkaline secondary batteries are discussed.
Details
- ISSN :
- 15726657
- Volume :
- 468
- Database :
- OpenAIRE
- Journal :
- Journal of Electroanalytical Chemistry
- Accession number :
- edsair.doi...........c916a10d85c9a7d04504424e8ca3f1b1
- Full Text :
- https://doi.org/10.1016/s0022-0728(99)00029-7