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Palladium/Cobalt Coated on Multi‐Walled Carbon Nanotubes as an Electro‐catalyst for Oxygen Reduction Reaction in Passive Direct Methanol Fuel Cells
19
Citations
86
References
2013
Year
Materials ScienceOxygen Reduction ReactionChemical EngineeringCatalytic ApplicationEngineeringMulti‐walled Carbon NanotubesSurface ElectrochemistryNanoheterogeneous CatalysisCatalysisBatteriesChemistryCatalyst PreparationElectrochemical ProcessAccelerated Durability TestPd‐based Alloy ElectrocatalystsPalladium/cobalt CoatedElectrochemistry
Abstract This work reports the synthesis of Pd‐based alloy electrocatalysts of Co supported on multi‐walled carbon nanotubes (MWCNTs) and their evaluation as cathode materials in a passive direct methanol fuel cell (PDMFC). The X‐ray diffraction (XRD) analysis showed well‐defined reflections corresponding to a face centered cubic phase of palladium. As compared to the Pd/MWCNT electrocatalyst, the bimetallic alloy electrocatalysts with the different Pd x Co atomic ratios showed highly enhanced mass activity (MA) for the oxygen reduction reaction (ORR); however, the significant enhancement in the specific activity (SA) by a factor of about 1.2–5.6 for the ORR was found on the Pd x Co alloy electrocatalysts in the presence and absence of methanol electrolyte solution. This enhancement SA in of the Pd‐based electrocatalysts was correlated to the changes in the lattice parameter and Pd x Co surface composition. Surface area changes of Pd‐based electrocatalysts supported on MWCNT were evaluated using an accelerated durability test (ADT). The results obtained using the ADT were correlated to the performance of the Pd‐based electrocatalysts in the PDMFC. A better performance was obtained for the cell using Pd 3 Co/MWCNT (2.53 mW cm –2 ) compared to Pd/MWCNT (1.64 mW cm –2 ) and Pt/C‐Electrochem (1.20 mW cm –2 ) as cathode in the PDMFC. In the presence and absence of methanol the impedance Bode spectra showed one time constant that associated to follow a four electron pathway.
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