Thermodynamic and Kinetic Considerations for Ethanol Electrooxidation in Direct Ethanol Fuel Cells
β Scribed by Shuqin SONG; Yi WANG; Peikang SHEN
- Publisher
- Elsevier Science
- Year
- 2007
- Weight
- 533 KB
- Volume
- 28
- Category
- Article
- ISSN
- 1872-2067
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β¦ Synopsis
Thermodynamic and kinetic considerations for the ethanol electrooxidation in a proton exchange membrane fuel cell (PEMFC) were discussed. Theoretical calculations show that direct ethanol fuel cells (DEFCs) exhibit better exergic efficiency than ethanol reforming PEMFC. The thermodynamic analysis show that when temperature is lower than 100ΒΊC, the conversion of ethanol steam reforming is less than 14% for ethanol complete oxidation. The kinetic study shows that PtSn/C anodes have a relatively high activity for ethanol electrooxidation, but such activity is not high enough for ethanol complete electrooxidation. The thermodynamic and kinetic analyses suggest that the cell temperature is one of the key factors for the DEFC development.
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Owing to the formation of an oxametallacyclic conformation, the CeC bond cleavage is the preferential channel for the ethanol dissociation on the Rh surface, the addition of Rh to Pt can increase the CO 2 yield during the ethanol oxidation. However, in acidic media the slow oxidation kinetics of CO
## Abstract A series of hybrid protonβconducting membranes with an interpenetrating polymer network (IPN) structure was designed with the direct ethanol fuel cell (DEFC) application in mind. In these membranes, glutaraldehyde crosslinked poly(vinyl alcohol) (PVA) were interpenetrated with the copol