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The Electrochemical Society, Journal of The Electrochemical Society, 2(163), p. F25-F37, 2015

DOI: 10.1149/2.0141602jes

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2-Sulfoethylammonium Trifluoromethanesulfonate as an Ionic Liquid for High Temperature PEM Fuel Cells

This paper is available in a repository.
This paper is available in a repository.

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Abstract

2-Sulfoethylammonium trifluoromethanesulfonate ([2-Sea+][TfO-]) represents a novel class of proton-conducting ionic liquids (PILs) based on aminoalkylsulfonic acids. The fundamental suitability of [2-Sea+][TfO-] for application as a protic electrolyte in high temperature PEM fuel cells (HT-PEFCs) was investigated up to a temperature of 130°C. A comparison was made against a state-of-the-art electrolyte, phosphoric acid. [2-Sea+][TfO-] is electrochemically and thermally stable up to 140°C. The specific conductivity of 95 wt% [2-Sea+][TfO-] aqueous solution at 130°C is ≈20 times lower compared to 95 wt% H3PO4. The strong coupling of ion transport and viscous flow suggests a vehicular ion (proton) transport in [2-Sea+][TfO-]. 95 wt% [2-Sea+][TfO-] shows superior kinetics in terms of oxygen reduction reaction (ORR) on polycrystalline Pt compared to 95 wt% H3PO4 at temperatures greater than 90°C in a fuel cell-applicable potential range. Double layer capacitances suggest a complex double layer structure, including adsorbed [2-Sea+][TfO-] and water, as well as intermediates of oxygen reduction and Pt oxidation. Potential and temperature-dependent ORR kinetics in the presence of 95 wt% [2-Sea+][TfO-] yield different Tafel slopes (b = 82-139 mV) and symmetry factors (β = 0.46-0.96), indicating changes in surface coverages of the adsorbed species and possibly also a change in the reaction mechanism.