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Issue 1, 1984
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X-ray photoelectron spectroscopic studies of the iridium electrode system


X-ray photoelectron spectroscopy has been used to investigate the surface of iridium electrodes studied under both steady-state and cyclic conditions in 0.5 and 5 mol dm–3 sulphuric acid solutions. The results show that pulsing into the anodic region produced very small amounts of oxide in 0.5 mol dm–3 acid and slightly more in the 5 mol dm–3 solutions. The oxide is thought to be predominantly IrO2. When the electrode has been cycled up to 1.5 V (vs RHE) substantial amounts of oxide were observed, the amount being dependent upon the number of cycles and the sweep rate. The oxide was not a simple as in the case of polarization, but is explained as a mixture of iridium oxy/hydroxide species. Two other sweep limits (1.2 and 1.8 V) were briefly investigated. Possible mechanisms explaining these results are discussed. The pure-metal spectra (including angle-resolved studies) have been examined at ambient and elevated temperatures with particular emphasis upon the O 1s region and the methods for removing any residual oxide from the metal surface.

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Article type: Paper
DOI: 10.1039/F19848000135
Citation: J. Chem. Soc., Faraday Trans. 1, 1984,80, 135-152

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    X-ray photoelectron spectroscopic studies of the iridium electrode system

    H. Y. Hall and P. M. A. Sherwood, J. Chem. Soc., Faraday Trans. 1, 1984, 80, 135
    DOI: 10.1039/F19848000135

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