Journal Article FZJ-2022-02099

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Tuning Polybenzimidazole Membrane by Immobilizing a Novel Ionic Liquid with Superior Oxygen Reduction Reaction Kinetics

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2022
American Chemical Society Washington, DC

Chemistry of materials 34(10), acs.chemmater.1c03819 () [10.1021/acs.chemmater.1c03819]

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Abstract: Protic ionic liquid (PIL) is a promising nonaqueous electrolyte alternative to replacing phosphoric acid for fuel cells operating at temperatures above 100 °C. In this study, the physical and electrochemical properties of stoichiometric and nonstoichiometric PILs are investigated focusing on their acid/base ratio. The study involves a series of PILs, generically indicated as N,N-diethyl-3-sulfopropane-1-ammonium trifluoromethanesulfonate ([DESPA+][TfO–]), varying from an excess of the proton acceptor (N,N-diethyl-3-aminopropane-1-sulfonic acid) to an excess of the proton donor (trifluoromethanesulfonic acid, TfOH). Compared to a state-of-the-art electrolyte, i.e., concentrated phosphoric acid, the nonstoichiometric [DESPA+][TfO–] shows superior oxygen reduction reaction kinetics on the investigated Pt catalysts and oxygen permeation ability (DO2·cO2). [DESPA+][TfO–] with a base-to-acid molar ratio of 1:2 achieves a current density ∼10 times larger than that of concentrated phosphoric acid at 110 °C and 0.8 V. Membranes including polybenzimidazole as a host polymer and stoichiometric and nonstoichiometric [DESPA+][TfO–] as the conductive electrolyte exhibit promising properties in terms of thermal stability and conductivity. At 120 °C and 40% relative humidity, conductivities of 2 and 16 mS cm–1 are achieved by the membranes employing stoichiometric and excess acid [DESPA+][TfO–], respectively.

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Contributing Institute(s):
  1. Elektrochemische Verfahrenstechnik (IEK-14)
Research Program(s):
  1. 1231 - Electrochemistry for Hydrogen (POF4-123) (POF4-123)

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Dokumenttypen > Aufsätze > Zeitschriftenaufsätze
Institutssammlungen > IET > IET-4
Workflowsammlungen > Öffentliche Einträge
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Open Access

 Datensatz erzeugt am 2022-05-05, letzte Änderung am 2024-07-12


Published on 2022-05-03. Available in OpenAccess from 2023-05-03.:
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