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| Content Provider | Royal Society of Chemistry (RSC) |
|---|---|
| Author | Zhang, Genlei Yang, Zhenzhen Zhang, Wen Wang, Yuxin |
| Copyright Year | 2017 |
| Abstract | The direct methanol fuel cell is an emerging energy conversion device for which Pt is considered as the state-of-the-art anode catalyst. Herein, we show that the activity and stability of Pt for methanol oxidation can be significantly enhanced using Mo-doped CeO2 (Ce1−xMoxO2−δ) solid solutions as co-catalysts. X-ray photoelectron spectroscopy (XPS) reveals a strong electronic interaction between Ce1−xMoxO2−δ and Pt in Pt/Ce1−xMoxO2−δ–C catalysts. Among all Pt/Ce1−xMoxO2−δ–C catalysts, the catalyst with a Ce/Mo atomic ratio of 7/3 (Pt/Ce0.7Mo0.3O2−δ–C) exhibits the highest activity, up to 1888.4 mA mgPt−1, which is one of the best results reported so far. A direct methanol fuel cell incorporating the Pt/Ce0.7Mo0.3O2−δ–C as the anode catalyst exhibits a maximum power density of 69.4 mW cm−2, which is 1.8 times that of an analogous fuel cell using the commercial Pt/C-JM as the anode catalyst. |
| Starting Page | 1481 |
| Ending Page | 1487 |
| Page Count | 7 |
| File Format | HTM / HTML PDF |
| ISSN | 20507488 |
| Volume Number | 5 |
| Issue Number | 4 |
| Journal | Journal of Materials Chemistry A |
| DOI | 10.1039/c6ta09043e |
| Language | English |
| Publisher | Royal Society of Chemistry |
| Access Restriction | Open |
| Subject Keyword | Direct methanol fuel cell Energy transformation Anode Methanol X-ray photoelectron spectroscopy Photoemission spectroscopy Fuel cell |
| Content Type | Text |
| Resource Type | Article |
| Subject | Chemistry Renewable Energy, Sustainability and the Environment Materials Science |
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