2-Sulfoethylammonium Trifluoromethanesulfonate as an Ionic Liquid for High Temperature PEM Fuel Cells
Author(s) -
Klaus Wippermann,
Jürgen Wackerl,
Werner Lehnert,
Benjamin Huber,
Carsten Korte
Publication year - 2015
Publication title -
journal of the electrochemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.258
H-Index - 271
eISSN - 1945-7111
pISSN - 0013-4651
DOI - 10.1149/2.0141602jes
Subject(s) - trifluoromethanesulfonate , electrolyte , chemistry , proton exchange membrane fuel cell , electrochemistry , adsorption , tafel equation , aqueous solution , phosphoric acid , inorganic chemistry , analytical chemistry (journal) , catalysis , organic chemistry , electrode
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
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