Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/57000
Title: An Investigation of a Polydopamine-Graphene Oxide Composite as a Support for an Anode Fuel Cell Catalyst
Authors: Aunanong Pinithchaisakula
Suwaphid Themsirimongkon
Napapha Promsawan
Paralee Weankeaw
Kontad Ounnunkad
Surin Saipanya
Authors: Aunanong Pinithchaisakula
Suwaphid Themsirimongkon
Napapha Promsawan
Paralee Weankeaw
Kontad Ounnunkad
Surin Saipanya
Keywords: Chemistry
Issue Date: 1-Jan-2017
Abstract: © 2016, Springer Science+Business Media New York. 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 (xPtPd/GO and xPtPd/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 xPtPd/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. [Figure not available: see fulltext.]
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85006355385&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/57000
ISSN: 18685994
18682529
Appears in Collections:CMUL: Journal Articles

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