Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/7678
Title: Conducting carbon/polymer composites as a catalyst support for proton exchange membrane fuel cells
Authors: Memioglu, F.
Bayrakçeken, A.
Öznülüer, T.
Ak, Metin
Keywords: Carbon corrosion
Conducting carbon/polymer composite
Durability
Electrical conductivity
PEM fuel cell
Carbon
Catalyst supports
Conductive plastics
Corrosion resistance
Cyclic voltammetry
Dimethyl sulfoxide
Electric conductivity
Electrolytic reduction
Ethylene
Ethylene glycol
Fourier transform infrared spectroscopy
Polyols
Proton exchange membrane fuel cells (PEMFC)
Scanning electron microscopy
Thermogravimetric analysis
X ray diffraction
Carbon-supported catalysts
Carbon/polymer composites
Chemical oxidative polymerization
Four-point probe techniques
Microwave irradiation techniques
Electrochemical oxidation
Publisher: John Wiley and Sons Ltd
Abstract: Carbon/poly(3,4-ethylene dioxythiophene) (C/PEDOT) composites are synthesized by in situ chemical oxidative polymerization of EDOT monomer on carbon black in order to decrease carbon corrosion that occurred in carbon-supported catalysts used in proton exchange membrane fuel cell. The effects of different dopants including polystyrene sulfonic acid, p-toluenesulfonic acid and camphorsulfonic acid with the addition of ethylene glycol or dimethyl sulfoxide on the properties of the composites are investigated. The synthesized composites are characterized by X-ray diffraction, Fourier transform infrared spectroscopy, thermogravimetric analysis, surface area analysis and scanning electron microscope. Electrical conductivity is determined by using the four-point probe technique. Electrochemical oxidation characteristics of the synthesized C/PEDOT composites are investigated by cyclic voltammetry by applying 1.2V for 24h. The composite prepared at 25°C with p-toluenesulfonic acid and ethylene glycol shows the best carbon corrosion resistance. Platinum-supported catalyst by using this composite was prepared using microwave irradiation technique, and it was seen that the prepared catalyst did not significantly lose its hydrogen oxidation and oxygen reduction reaction activities after electrochemical oxidation. © 2013 John Wiley & Sons, Ltd.
URI: https://hdl.handle.net/11499/7678
https://doi.org/10.1002/er.3126
ISSN: 0363-907X
Appears in Collections:Fen-Edebiyat Fakültesi Koleksiyonu
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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