The Comparability of Pt to Pt‐Ru in Catalyzing the Hydrogen Oxidation Reaction for Alkaline Polymer Electrolyte Fuel Cells Operated at 80 °C

The Pt‐catalyzed hydrogen oxidation reaction (HOR) for alkaline polymer electrolyte fuel cells (APEFCs) has been one of the focus subjects in current fuel‐cell research. The Pt catalyst is inferior for HOR in alkaline solutions, and alloying with Ru is an effective promotion strategy. APEFCs with Pt...

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Published inAngewandte Chemie Vol. 131; no. 5; pp. 1456 - 1460
Main Authors Li, Qihao, Peng, Hanqing, Wang, Yingming, Xiao, Li, Lu, Juntao, Zhuang, Lin
Format Journal Article
LanguageEnglish
Published Weinheim Wiley Subscription Services, Inc 28.01.2019
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Summary:The Pt‐catalyzed hydrogen oxidation reaction (HOR) for alkaline polymer electrolyte fuel cells (APEFCs) has been one of the focus subjects in current fuel‐cell research. The Pt catalyst is inferior for HOR in alkaline solutions, and alloying with Ru is an effective promotion strategy. APEFCs with Pt‐Ru anodes have provided a performance benchmark over 1 W cm−2 at 60 °C. The Pt anode is now found to be in fact as good as the Pt‐Ru anode for APEFCs operated at elevated conditions. At 80 °C with appropriate gas back‐pressure, the cell with a Pt anode exhibits a peak power density of about 1.9 W cm−2, which is very close to that with a Pt‐Ru anode. Even by decreasing the anode Pt loading to 0.1 mg cm−2, over 1.5 W cm−2 can still be achieved at 80 °C. This finding alters the previous understanding about the Pt catalyzed HOR in alkaline media and casts a new light on the development of practical and high‐power APFEC technology. Alkalische Polymerelektrolyt‐Brennstoffzellen (APEFCs) mit Pt‐Ru‐Anoden erreichen über 1 W cm−2 bei 60 °C. Für eine Pt‐Anode (grau) wird nun gefunden, dass sie in APEFCs mit erhöhter Betriebstemperatur ebenso gut wie die Pt‐Ru‐Anode (rot) ist. Bei T=80 °C und mit einem geeigneten Gasdruck p ergab eine Zelle mit Pt‐Anode eine Spitzenleistungsdichte von ca. 1.9 W cm−2 und kam dadurch der Zelle mit Pt‐Ru‐Anode sehr nahe.
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ISSN:0044-8249
1521-3757
DOI:10.1002/ange.201812662