An Investigation of a Polydopamine-Graphene Oxide Composite as a Support for an Anode Fuel Cell Catalyst

Home-made graphene oxide (GO) with a high surface area was functionalized by polydopamine (PDA) and was labeled PDA-GO, while GO without PDA was labeled as GO. With different compositions of metals (Pt and/or Pd), the electrodeposition of the metals onto the prepared GO and PDA-GO supports was prepa...

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Veröffentlicht in:Electrocatalysis 2017, Vol.8 (1), p.36-45
Hauptverfasser: Pinithchaisakula, Aunanong, Themsirimongkon, Suwaphid, Promsawan, Napapha, Weankeaw, Paralee, Ounnunkad, Kontad, Saipanya, Surin
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Sprache:eng
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Zusammenfassung:Home-made graphene oxide (GO) with a high surface area was functionalized by polydopamine (PDA) and was labeled PDA-GO, while GO without PDA was labeled as GO. With different compositions of metals (Pt and/or Pd), the electrodeposition of the metals onto the prepared GO and PDA-GO supports was prepared for the anode electrocatalyst. The electrocatalytic activities of the electrocatalysts ( x PtPd/GO and x PtPd/PDA-GO, where x  = 1–5) were studied in the oxidation of alcohols (e.g., methanol and ethanol). Morphologies obtained from transmission electron microscopy (TEM), scanning electron microscopy (SEM), and atomic force microscopy (AFM) images showed that the as-prepared GO and PDA-GO supports can accommodate electrodeposited metals loaded on the topmost layer of the support surfaces, although the size of nanoparticles is somewhat different. The electrochemical results indicated that the x PtPd/PDA-GO catalysts offered outstanding oxidation efficiencies. The prepared 5PtPd/PDA-GO catalyst provided enhanced activity and long-time stability in the oxidation reactions. The GO surface modified by the polymer and the other electrodeposited metal catalysts provided a larger number of available active sites, as the PDA offered a greater electric connection between the metal catalysts and the GO support during alcohol oxidation. Graphical Abstract Optimising ECL Production Through Careful Selection of Co-Reactions Based on Energetics Involved
ISSN:1868-2529
1868-5994
DOI:10.1007/s12678-016-0338-6