Abstract
A carbon-supported Pt catalyst (40 wt.% loading) is prepared by a modified ethylene glycol reduction method (Pt-EG-complex). In this procedure, a complex produced by reacting ethylene glycol with sodium borohydride (NaBH4), serves as a reducing agent for the Pt precursor and as a stabilizer for preventing the growth of Pt particles. For purposes of comparison, two types of carbon-supported Pt catalyst (40 wt.% loading) are also prepared by a NaBH4 reduction method, in which the Pt precursor is reduced in a ethylene glycol solution (Pt-EG-NaBH4) and in de-ionized water (Pt-H2O-NaBH4). Analysis by X-ray diffraction and transmission electron microscopy reveal that the Pt-EG-complex catalyst is comprised of highly-dispersed Pt nanoparticles with a uniform size (2.9-3.1 nm) on the carbon support, while large Pt particles are observed in the Pt-EG-NaBH4 (3.3-3.6 nm) and Pt-H2O-NaBH4 (5.7-6.2 nm) catalysts. The Pt-EG-complex catalyst has the highest electrochemical surface area and shows the highest catalytic performance for methanol electro-oxidation.
| Original language | English |
|---|---|
| Pages (from-to) | 987-990 |
| Number of pages | 4 |
| Journal | Journal of Power Sources |
| Volume | 160 |
| Issue number | 2 SPEC. ISS. |
| DOIs | |
| State | Published - 2006.10.6 |
Keywords
- Carbon-supported platinum catalyst
- Ethylene glycol reduction
- Methanol electro-oxidation
- Nanoparticles
- Sodium borohydride
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