| Literature DB >> 25351412 |
Katsutoshi Sato1, Sho Yagi, Shuhei Zaitsu, Godai Kitayama, Yuto Kayada, Kentaro Teramura, Yusaku Takita, Katsutoshi Nagaoka.
Abstract
In polymer electrolyte fuel cell (PEFC) systems, small amounts of ammonia (NH3 ) present in the reformate gas deactivate the supported ruthenium catalysts used for preferential oxidation (PROX) of carbon monoxide (CO). In this study, we investigated how the addition of a small amount of platinum to a Ru/α-Al2 O3 catalyst (Pt/Ru=1:9 w/w) affected the catalyst's PROX activity in both the absence and the presence of NH3 (130 ppm) under conditions mimicking the reformate conditions during steam reforming of natural gas. The activity of undoped Ru/α-Al2 O3 decreased sharply upon addition of NH3 , whereas Pt/Ru/α-Al2 O3 exhibited excellent PROX activity even in the presence of NH3 . Ruthenium K-edge X-ray absorption near-edge structure (XANES) spectra indicated that in the presence of NH3 , some of the ruthenium in the undoped catalyst was oxidized in the presence of NH3 , whereas ruthenium oxidation was not observed with Pt/Ru/α-Al2 O3 . These results suggest that ruthenium oxidation is retarded by the platinum, so that the catalyst shows high activity even in the presence of NH3 .Entities:
Keywords: X-ray absorption spectroscopy; fuel cells; heterogeneous catalysis; hydrogen; natural gas
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Year: 2014 PMID: 25351412 DOI: 10.1002/cssc.201402583
Source DB: PubMed Journal: ChemSusChem ISSN: 1864-5631 Impact factor: 8.928