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Synthesis of New Protic Ionic Liquids for Fuel Cells on the Basis of In-Situ FT-IR Measurements

机译:基于原位FT-IR测量的燃料电池新质子离子液体的合成

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A series of protic ionic liquids (ILs) were synthesized from N,Ndiethylmethylamine (dema) and three kinds of imides having different fluoroalkyl chain lengths (H-N(SO_2(CF_2)_nF)_2, n = 0-2) as electrolytes for fuel cells. The effect of anion structure on the oxygen reduction reaction (ORR) activity of Pt electrode was investigated in detail using the prepared ILs. As increasing n of imide-anion, the ORR current was increased. The onset potential for ORR was also shifted towards the positive side as extending the fluoroalkyl chain of imide-anion. This potential shift was clearly revealed by in-situ FT-IR measurement to relate the anion adsorbability on the Pt electrode, depending on the fluoroalkyl chain length of imide structure.
机译:由N,Ndiethylethylamine(dema)和三种具有不同氟烷基链长的酰亚胺(HN(SO_2(CF_2)_nF)_2,n = 0-2)合成的一系列质子离子液体(ILs)用作燃料电池的电解质。使用制备的离子液体详细研究了阴离子结构对Pt电极的氧还原反应(ORR)活性的影响。随着酰亚胺阴离子n的增加,ORR电流增加。随着延伸酰亚胺阴离子的氟烷基链,ORR的起始电位也移向正侧。根据酰亚胺结构的氟代烷基链长度,通过原位FT-IR测量清楚地揭示了这种电位偏移,从而将阴离子吸附在Pt电极上。

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