4.7 Article Proceedings Paper

Novel composite membrane based on zirconium phosphate-ionic liquids for high temperature PEM fuel cells

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 46, Issue 8, Pages 6100-6109

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2020.02.112

Keywords

Imidazolium ionic liquids; Zirconium phosphate (ZrP); Composite membranes; High temperature fuel cells; Proton conductivity; PEM fuel cells

Funding

  1. American University of Sharjah, United Arab Emirates [FRG16-R-16]

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The synthesized composite membrane exhibits high proton conductivity at elevated temperatures, making it a promising candidate for use in PEM fuel cells. The composite membranes have the potential for stable proton conductivity and may be suitable for application in high-temperature PEM fuel cells.
Composite membranes composed of zirconium phosphate (ZrP) and imidazolium-based ionic liquids (IL), supported on polytetrafluoroethylene (PTFE) were prepared and evaluated for their application in proton exchange membrane fuel cells (PEM) operating at 200 degrees C. The experimental results reported here demonstrate that the synthesized membrane has a high proton conductivity of 0.07 S cm-1, i.e, 70% of that reported for Nafion. Furthermore, the composite membranes possess a very high proton conductivity of 0.06 S cm(-1) when processed at 200 degrees C under completely anhydrous conditions. Scanning electron microscopy (SEM) images indicate the formation of very small particles, with diameters in the range of 100-300 nm, within the confined pores of PTFE. Thermogravimetric analysis (TGA) reveals a maximum of 20% weight loss up to 500 degrees C for the synthesized membrane. The increase in proton conductivity is attributed to the creation of multiple proton conducting paths within the membrane matrix. The IL component is acting as a proton bridge. Therefore, these membranes have potential for use in PEM fuel cells operating at temperatures around 200 degrees C. (c) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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