In situ functionalisation of mesoporous carbon electrodes with carbon nanotubes for proton exchange membrane fuel-cell application
Autor: | Akram Maghsodi, Fatemeh Shoghi, Leila Samiee |
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Rok vydání: | 2014 |
Předmět: |
Materials science
Industrial catalysts chemistry.chemical_element Proton exchange membrane fuel cell Carbon nanotube Condensed Matter Physics law.invention Catalysis chemistry Chemical engineering law Specific surface area Organic chemistry General Materials Science Carbon nanotube supported catalyst Platinum Carbon |
Zdroj: | Materials Chemistry and Physics. 143:1228-1235 |
ISSN: | 0254-0584 |
DOI: | 10.1016/j.matchemphys.2013.11.027 |
Popis: | In the work presented here, an attempt is made to study the effect of different carbon supports on the mesostructural properties as well as electrochemical behaviour of Pt/carbon supports. In this respect, the functionalised samples have been synthesised by using CMK-3, nickelocene as nickel source and the chemical vapour deposition (CVD) process for growth of carbon nanotubes. The platinum catalysts (Pt 20 wt.%) were obtained through a conventional wet impregnation method. All the materials have been characterised by XRD (small- and high-) angle, N 2 adsorption–desorption isotherms, high-resolution transmission electron microscopy and high-resolution field emission scanning electron microscopy. The results showed that the mesostructural structure had been partially destroyed by functionalisation of CMK-3 with NiO and multiwalled carbon nanotubes (MWCNTs). Moreover, wide-angle X-ray diffraction (WAXRD) studies revealed the formation of smaller platinum crystallite sizes compared to Vulcan-supported samples. Furthermore, electrochemical evaluation indicates that CMK-3–CNT–20Pt gives a specific surface area of 58.9 m 2 g −1 . Finally, the polarisation curves for the fabricated membrane electrode assemblies (MEAs) with Pt loading of 0.5 mg cm −2 demonstrated that the CMK-3–CNT–20Pt catalyst shows better performance than industrial catalysts and even Vulcan–40% Pt. |
Databáze: | OpenAIRE |
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