PEDOT_PSS self-assembled films to methanol crossover reduction in Nafion registered membranes
Alternative energy sources are on a global demand, with fuel cells as promising devices from mobile to stationary applications. Nafion registered is at the heart of many of these appliances, being mostly used due to its high proton conduction and good chemical stability at ambient temperature in pro...
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Published in | Applied surface science Vol. 323; pp. 7 - 12 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
01.12.2014
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Subjects | |
Online Access | Get full text |
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Summary: | Alternative energy sources are on a global demand, with fuel cells as promising devices from mobile to stationary applications. Nafion registered is at the heart of many of these appliances, being mostly used due to its high proton conduction and good chemical stability at ambient temperature in proton exchange membranes (PEM). Therefore, methanol permeation throughout Nafion registered films reduces drastically the performance of direct methanol fuel cells (DMFC). We present here the deposition of layer-by-layer (LbL) nanostructured thin films of poly(allylamine hydrochloride) (PAH) and poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) (PEDOT:PSS) onto commercial Nafion registered 212 membranes. It was observed a good adherence of the LbL films onto Nafion registered 212, with UV-vis results displaying a linear characteristic growth, indicative that the same amount of material was deposited at each deposition step during the layer-by-layer assembly. In addition, the LbL films also act as a good barrier to avoid methanol crossover, with an observed reduction in the methanol permeation from 5.510-6 cm2 s-1 to 3.210-6 cm2 s-1, respectively to pristine Nafion registered 212 and a 5-bilayer PAH/PEDOT:PSS LbL film deposited on Nafion registered 212. The measured power density in a DMFC set-up was not significantly changed (12mWcm-2) due to the LbL films, since the PAH/PEDOT:PSS nanostructure is impeding water and ion transport, consequently affecting the proton conduction throughout the membrane. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 content type line 23 ObjectType-Feature-2 |
ISSN: | 0169-4332 |
DOI: | 10.1016/j.apsusc.2014.08.056 |