Abstract
In this work, the mechanism of the ethanol oxidation reaction (EOR) on a palladium electrode was studied using the cyclic voltammetry method. The dissociative adsorption of ethanol was found to proceed rather quickly and the rate-determining step was the removal of the adsorbed ethoxi by the adsorbed hydroxyl on the Pd electrode. The Tafel slope was found to be 130 mV dec-1 at lower potentials, which suggests that the adsorption of OH- ions follows the Temkin-type isotherm on the Pd electrode. In comparison, the Tafel slope increased gradually to 250 mV dec-1 at higher potentials. The change in the Tafel slope indicated that, at higher potentials, the kinetics is not only affected by the adsorption of the OH- ions, but also by the formation of the inactive oxide layer on the Pd electrode.
| Original language | English |
|---|---|
| Pages (from-to) | 2203-2208 |
| Number of pages | 6 |
| Journal | Electrochimica Acta |
| Volume | 54 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - 1 Mar 2009 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Alkaline
- Direct ethanol fuel cell (DEFC)
- Ethanol oxidation reaction (EOR)
- Mechanism
- Palladium
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