New fuels as alternatives to methanol for direct oxidation fuel cells

Citation
E. Peled et al., New fuels as alternatives to methanol for direct oxidation fuel cells, EL SOLID ST, 4(4), 2001, pp. A38-A41
Citations number
17
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
ELECTROCHEMICAL AND SOLID STATE LETTERS
ISSN journal
10990062 → ACNP
Volume
4
Issue
4
Year of publication
2001
Pages
A38 - A41
Database
ISI
SICI code
1099-0062(200104)4:4<A38:NFAATM>2.0.ZU;2-Q
Abstract
Hydrocarbons and aliphatic alcohols are difficult to electro-oxidize. Even at 190 degreesC the oxidation of ethanol is incomplete (less than 40% CO2). We report here, for the first time, on the complete electro-oxidation of t wo molecules having C-C bonds; ethylene glycol (EG) and dimethyl oxalate (D MO). Both are less prone to pass through the membrane, and, as a result, ha ve up to 94-95% fuel utilization, 9-10% higher than that of methanol. EG is well known in the automobile industry and, in contrast to methanol, its di stribution infrastructure already exists, making it a promising candidate f or practical electric vehicles. DMO is a solid that has limited solubility in water, thus it may be added directly to the anode compartment with no ne ed of a separate fuel tank and monitoring and feeding systems. It is projec ted that a flat dimethyl oxalate fuel cell will deliver up to 600 Wh/kg, fi ve to ten times the specific energy of the lithium-ion battery in small por table devices. However, methanol does have some advantages over EG and DMO, its theoretical capacity is 20 to 40% higher and so far it has higher ener gy conversion efficiency. (C) 2001 The Electrochemical Society.