Abstract
Direct formic acid fuel cells (DFAFC) currently employ either Pt-based or Pd-based anode catalysts for oxidation of formic acid. However, improvements are needed in either the activity of Pt-based catalysts or the stability of Pd-based catalysts. In this study, a number of carbon-supported Pt-based and Pd-based catalysts, were prepared by co-depositing PdM (M = Bi, Mo, or V) on Vulcan® XC-72 carbon black, or depositing another metal (Pb or Sn) on a Pt/C catalyst. These catalysts were systematically evaluated and compared with commercial Pd/C, PtRu/C, and Pt/C catalysts in a multi-anode DFAFC. The PtPb/C and PtSn/C catalysts were found to show significantly higher activities than the commercial Pt/C catalyst, while the PdBi/C provided higher stability than the commercial Pd/C catalyst.
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Acknowledgments
This study was supported by the Natural Sciences and Engineering Research Council of Canada (NSERC) through a Strategic Projects Grant in partnership with Tekion (Canada) Inc., and by Memorial University.
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Yu, X., Pickup, P.G. Screening of PdM and PtM catalysts in a multi-anode direct formic acid fuel cell. J Appl Electrochem 41, 589–597 (2011). https://doi.org/10.1007/s10800-011-0267-2
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DOI: https://doi.org/10.1007/s10800-011-0267-2