Herein we show that protic ionic liquids (PILs) are promising electrolytes for fuel cells operating in the temperature range 100−120 °C. N,N-Diethyl-N-methyl-3-sulfopropan-1-ammonium hydrogen sulfate ([DEMSPA][HSA]), N,N-diethyl-N-methyl-3-sulfopropan-1-ammonium triflate ([DEMSPA][TfO]), N,N-diethyl-3-sulfopropan-1-ammonium hydrogen sulfate ([DESPA][HSA]), and N,N-diethyl-3-sulfopropan-1-ammonium triflate ([DESPA][TfO]) are investigated in this study with regard to their specific conductivity, thermal stability, viscosity, and electrochemical properties. The [DEMSPA][TfO] and [DESPA][TfO] electrolytes offer high limiting current densities for the oxygen reduction reaction (ORR) on platinum electrodes, that is, about 1 order of magnitude larger than 98% H3PO4. This is explained by the minor poisoning of the Pt catalyst and the significantly larger product of the oxygen self-diffusion coefficient and concentration in these two PILs. © 2021 The Authors. Published by American Chemical Society
Acidic ionic liquids enabling intermediate temperature operation fuel cells / Hou, H.; Schütz, H. M.; Giffin, J.; Wippermann, K.; Gao, X.; Mariani, A.; Passerini, S.; Korte, C.. - In: ACS APPLIED MATERIALS & INTERFACES. - ISSN 1944-8244. - 13:7(2021), pp. 8370-8382. [10.1021/acsami.0c20679]
Acidic ionic liquids enabling intermediate temperature operation fuel cells
Passerini, S.
;
2021
Abstract
Herein we show that protic ionic liquids (PILs) are promising electrolytes for fuel cells operating in the temperature range 100−120 °C. N,N-Diethyl-N-methyl-3-sulfopropan-1-ammonium hydrogen sulfate ([DEMSPA][HSA]), N,N-diethyl-N-methyl-3-sulfopropan-1-ammonium triflate ([DEMSPA][TfO]), N,N-diethyl-3-sulfopropan-1-ammonium hydrogen sulfate ([DESPA][HSA]), and N,N-diethyl-3-sulfopropan-1-ammonium triflate ([DESPA][TfO]) are investigated in this study with regard to their specific conductivity, thermal stability, viscosity, and electrochemical properties. The [DEMSPA][TfO] and [DESPA][TfO] electrolytes offer high limiting current densities for the oxygen reduction reaction (ORR) on platinum electrodes, that is, about 1 order of magnitude larger than 98% H3PO4. This is explained by the minor poisoning of the Pt catalyst and the significantly larger product of the oxygen self-diffusion coefficient and concentration in these two PILs. © 2021 The Authors. Published by American Chemical SocietyFile | Dimensione | Formato | |
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