How To Make Electrocatalysts More Active for Direct Methanol OxidationAvoid PtRu Bimetallic Alloys
Contrary to the current understanding of Pt−Ru electrocatalyzed oxidation of methanol, the bimetallic alloy is not the most desired form of the catalyst. In the nanoscale Pt−Ru blacks used to electrooxidize methanol in direct methanol fuel cells, Pt0Ru0 has orders of magnitude less activity for meth...
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Veröffentlicht in: | The journal of physical chemistry. B 2000-10, Vol.104 (42), p.9772-9776 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Contrary to the current understanding of Pt−Ru electrocatalyzed oxidation of methanol, the bimetallic alloy is not the most desired form of the catalyst. In the nanoscale Pt−Ru blacks used to electrooxidize methanol in direct methanol fuel cells, Pt0Ru0 has orders of magnitude less activity for methanol oxidation than does a mixed-phase electrocatalyst containing Pt metal and hydrous ruthenium oxides (RuO x H y ). Bulk, rather than near-surface, quantities of electron−proton conducting RuO x H y are required to achieve high activity for methanol oxidation. The active catalyst forms a nanoscopic, phase-separated hydrons oxide-on-metal structure that retains the Pt metal−RuO x H y boundaries required to oxidize methanol fully to carbon dioxide and water. |
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ISSN: | 1520-6106 1520-5207 |
DOI: | 10.1021/jp001954e |