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    Enhancement of Pt and Pt-alloy fuel cell catalyst activity and durability via nitrogen-modified carbon supports

    Access Status
    Fulltext not available
    Authors
    Zhou, Y.
    Neyerlin, K.
    Olson, T.
    Pylypenko, S.
    Bult, J.
    Dinh, H.
    Gennett, T.
    Shao, Zongping
    O'Hayre, R.
    Date
    2010
    Type
    Journal Article
    
    Metadata
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    Citation
    Zhou, Y. and Neyerlin, K. and Olson, T. and Pylypenko, S. and Bult, J. and Dinh, H. and Gennett, T. et al. 2010. Enhancement of Pt and Pt-alloy fuel cell catalyst activity and durability via nitrogen-modified carbon supports. Energy and Environmental Science. 3 (10): pp. 1437-1446.
    Source Title
    Energy and Environmental Science
    DOI
    10.1039/c003710a
    ISSN
    1754-5692
    School
    Department of Chemical Engineering
    URI
    http://hdl.handle.net/20.500.11937/31660
    Collection
    • Curtin Research Publications
    Abstract

    Insufficient catalytic activity and durability are key barriers to the commercial deployment of low temperature polymer electrolyte membrane (PEM) and direct-methanol fuel cells (DMFCs). Recent observations suggest that carbon-based catalyst support materials can be systematically doped with nitrogen to create strong, beneficial catalyst-support interactions which substantially enhance catalyst activity and stability. Data suggest that nitrogen functional groups introduced into a carbon support appear to influence at least three aspects of the catalyst/support system: 1) modified nucleation and growth kinetics during catalyst nanoparticle deposition, which results in smaller catalyst particle size and increased catalyst particle dispersion, 2) increased support/catalyst chemical binding (or "tethering"), which results in enhanced durability, and 3) catalyst nanoparticle electronic structure modification, which enhances intrinsic catalytic activity. This review highlights recent studies that provide broad-based evidence for these nitrogen-modification effects as well as insights into the underlying fundamental mechanisms. © 2010 The Royal Society of Chemistry.

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