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Synthesis and Properties of Platinum Nanocatalyst Supported on Cellulose-Based Carbon Aerogel for Applications in PEMFCs
Platinum nanoparticles supported on nanostructured cellulose-based carbon aerogels (carbonized aerocellulose, CAC) were evaluated in proton exchange membrane fuel cell (PEMFC). The CAC substrate was synthesized through the dissolution, gelation, regeneration, supercritical CO2 drying and pyrolysis o...
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Published in: | Journal of the Electrochemical Society 2011, Vol.158 (7), p.B779-B789 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Platinum nanoparticles supported on nanostructured cellulose-based carbon aerogels (carbonized aerocellulose, CAC) were evaluated in proton exchange membrane fuel cell (PEMFC). The CAC substrate was synthesized through the dissolution, gelation, regeneration, supercritical CO2 drying and pyrolysis of cellulose. The Pt nanoparticles deposition was performed by impregnation of the CAC with H2PtCl6, followed by Pt z species reduction either under H2 at 300-400C or in basic NaBH4 solution. While H2 reduction leads to uniform Pt nanoparticles well-dispersed over the CAC surface, larger agglomerates form with NaBH4 reduction, as revealed by transmission electron microscopy (TEM) and powder X-ray diffraction (XRD). The reduction methods influences the quantity of platinum deposited, which may be increased by using multiple impregnation/reduction steps. The specific surface area of Pt and specific/mass activities towards oxygen reduction of the Pt/CAC materials, investigated using the rotating disk electrode setup, are similar to those of commercial Pt/Carbon Black (CB). Finally, PEMFC unit cell testing demonstrates that a Pt/CAC sample synthesized using three successive impregnation/reduction steps, loaded at ca. 14 wt Pt/(Pt C), competes with state-of-the-art Pt/CB electrocatalysts of comparable Pt loading |
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ISSN: | 0013-4651 1945-7111 |
DOI: | 10.1149/1.3585744 |