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- 2007 Annual Meeting
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- Carbon Nanotubes IV
- (218f) Functionalization Of Carbon Nanotubes And Carbon Nanofibers Via Supercritical Fluid Treatment For Use In Fuel Cells
These methods eliminate the need for any harsh oxidative or UV treatments typically used to functionalize SWCNTs and CNFs [2, 3]. We have recently evaluated Pt functionalized SWCNTs and CNFs using this technique with anode Pt loadings of 0.57 mg/cm2 and 0.55 mg/cm2 respectively. Although the peak power density of the CNF membrane electrode assembly (MEA) was 334 mW/cm2, which is slightly less than the SWCNT MEA (396 mW/cm2), the results are encouraging for the usage of CNFs as a substitute for the more expensive SWCNTs [4]. Improvements in synthesis conditions have revealed average Pt particle diameter of 3.1 nm with a standard deviation of 2.6 nm. With a goal of increasing the Pt utilization for these supports, we will characterize our synthesis conditions with the particle size, electrochemical active surface area, and fuel cell performance and compare our results to standard MEAs using conventional catalysts.
References:
1. Melechko, A.V., et al., Vertically aligned carbon nanofibers and related structures: Controlled synthesis and directed assembly. Journal of Applied Physics, 2005. 97(4).
2. Sun, Z.Y., et al., Synthesis of noble metal/carbon nanotube composites in supercritical methanol. Journal of Nanoscience and Nanotechnology, 2006. 6(3): p. 691-697.
3. Quinn, B.M., C. Dekker, and S.G. Lemay, Electrodeposition of noble metal nanoparticles on carbon nanotubes. Journal of the American Chemical Society, 2005. 127(17): p. 6146-6147.
4. Guo, J.S., et al., Carbon nanofibers supported Pt-Ru electrocatalysts for direct methanol fuel cells. Carbon, 2006. 44(1): p. 152-157.