4.4 Article

Effect of heat treatment on PtRu/C catalyst for methanol electro-oxidation

Journal

JOURNAL OF APPLIED ELECTROCHEMISTRY
Volume 39, Issue 9, Pages 1503-1508

Publisher

SPRINGER
DOI: 10.1007/s10800-009-9833-2

Keywords

PtRu/C; Methanol electro-oxidation; Electrocatalyst; CO stripping; X-ray photoelectron spectroscopy

Funding

  1. Center for Ultramicrochemical Process Systems (CUPS)
  2. KOSEF (2008)
  3. Ministry of Education, Science & Technology (MoST), Republic of Korea [N01090032] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  4. Ministry of Knowledge Economy (MKE), Republic of Korea [10029897] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  5. National Research Foundation of Korea [과C6A1907, 2004-0043258] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The effect of heat treatment on a commercial PtRu/C catalyst was investigated with a focus on the relationship between electrochemical and surface properties. The heat treated PtRu/C catalysts were prepared by reducing the commercial PtRu/C catalyst at 300, 500, and 600 A degrees C under hydrogen flow. The maximum mass activity for the methanol electro-oxidation reaction (MOR) was observed in the catalyst heat treated at 500 A degrees C, while specific activity for the MOR increased with increasing heat treatment temperature. Cyclic voltammetry (CV) results revealed that the heat treatment caused Pt rich surface formation. The increase in surface Pt was confirmed by X-ray photoelectron spectroscopy; the surface (Pt:Ru) ratio of the fresh catalyst (81:19) changed to (87:13) in the 600 A degrees C heat treated catalyst. Quantitative analysis of the Ru oxidation state showed that the ratio of metallic Ru increased with an increase in heat treatment temperature. On the other hand, RuOxHy completely reduced at 500 A degrees C and the ratio of RuO2 slightly decreased with increasing heat treatment temperature.

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