4.7 Article

Endurance strategies for the preparation of high temperature polymer electrolyte membranes by UV polymerization of 1-H-3-vinylimidazolium bis(trifluoromethanesulfonyl)imide for fuel cell applications

期刊

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 41, 期 6, 页码 3981-3993

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2015.11.006

关键词

Polymeric ionic liquids; Imidazolium; Cross-linking; Polybenzimidazole; UV induced polymerization; Ion conductive membranes

资金

  1. European Commission [209481]

向作者/读者索取更多资源

This work pursues the enhancement of durability of polymeric ionic liquid (PIL) membranes prepared by ultraviolet (UV) radiation-induced polymerization for high temperature proton exchange membrane fuel cell (HT-PEMFC) applications. In particular, the co-polymerization of 1-H-3-vinylimidazolium bis(trifluoromethanesulfonyl)imide [HVIm] [TFSI] with divinylbenzene used as crosslinker (CL) or the in situ UV polymerization on a preexisting randomly porous polybenzimidazole (PBI) matrix as novel preparation methods in this field, have been fully studied and compared as endurance strategies. A comprehensive characterization of these new ion conducting membranes based on PILs, including methanol permeability and fuel cell (FC) performance, has been accomplished. The prepared membranes exhibited extremely high ion conductivity values, i.e. above 400 mS cm(-1) at 200 degrees C, in absence of H2O and H3PO4 molecules as proton carriers. The conduction endurance properties of these outstanding membranes were evaluated at 200 degrees C for more than 40 days. Performance losses were observed during the first 500 h; afterwards, the conductivity values remained almost constant above 250 mS cm-1. The cross-linked PIL membranes achieved current densities of 57.8 mA cm(-2) 0.5 V under anhydrous conditions at 120 degrees C whereas infiltrated PIL on PBI porous supports provided current densities of 46.9 mA cm(-2) at the same conditions. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.

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