Oxygen overvoltage measurements were made on bright gold electrodes in oxygen saturated 2 N H,SO, solutions to which H,O, was added until the HsOp concentration was O-1 M. It was found that the H,O&abilired systems produced a much more 'reversible' electrode, most likely because steps involving the
Oxygen overvoltage on bright gold—I
✍ Scribed by J.P. Hoare
- Publisher
- Elsevier Science
- Year
- 1966
- Tongue
- English
- Weight
- 609 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0013-4686
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✦ Synopsis
Oxygen overvoltage measurements have been made on Au/Au-O and Au/Au,08 electrodes in oxygen-saturated 2 N sulphuric acid solution. The rate-determining step in the reduction of oxygen on an Au/Au-O electrode is O,(ads) + e + O,-(ads), with an i,, of I.3 x lo-l1 A/cm*. An Au/Au-O electrode is a poly-electrode system, and the opencircuit corrosion current is 3.6 x 1O-8 A/cm%. Oxygen evolution could not be studied on an Au/Au-0 electode because the anodization process converts the electrode to an Au/Au,O, electrode. The Au/Au,Oll electrode is a single electrode system with an E0 of + 1.360 V, and the electrode process is the formation and reduction of Au,Os, AttaOs + 6H+ -I-6e z= 2Au + 3H80.
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