Proton conducting membranes based on semi-interpenetrating polymer network of NafionA+ and polybenzimidazole
A new strategy to prepare the reinforced composite membranes for polymer electrolyte membrane fuel cells (PEMFCs), which can work both in humidified and anhydrous state, was proposed via constructing semi-interpenetrating polymer network (semi-IPN) structure from polybenzimidazole (PBI) and NafionA+...
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Veröffentlicht in: | Polymer (Guilford) 2010-10, Vol.51 (23), p.5473-5481 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A new strategy to prepare the reinforced composite membranes for polymer electrolyte membrane fuel cells (PEMFCs), which can work both in humidified and anhydrous state, was proposed via constructing semi-interpenetrating polymer network (semi-IPN) structure from polybenzimidazole (PBI) and NafionA+212, with N-vinylimidazole as the crosslinker. The crosslinkable PBI was synthesized from poly(2,2a super(2)-(m-phenylene)-5,5a super(2)-bibe nzimidazole) and p-vinylbenzyl chloride. The semi-IPN structure was formed during the membrane preparation. The composite membranes exhibit excellent thermal stability, high-dimensional stability, and significantly improved mechanical properties compared with NafionA+212. The proton transport in the hydrated composite membranes is mainly contributed by the vehicle mechanism, with proton conductivity from a1410a2 S/cm to a1410a1 S/cm. When the temperature exceeds 100AC, the proton conductivity of the semi-IPN membranes decreases quickly due to the dehydration of the membranes. Under anhydrous condition, the proton conductivity of the membranes will drop to a1410a4 S/cm, which is also useful for intermediate temperature (100-200AC) PEMFCs. The benzimidazole structure of PBI and the acidic component of NafionA+ provide the possibility for the proton mobility via structure diffusion involving proton transfer between the heterocycles with a corresponding reorganization of the hydrogen bonded network. Display Omitted |
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ISSN: | 0032-3861 |
DOI: | 10.1016/j.polymer.2010.09.057 |