Department of Chemistry and Biotechnology, Yokohama National University, 79-5 Tokiwadai, Hodogaya-ku, Yokohama 240-8501, Japan.
J Am Chem Soc. 2010 Jul 21;132(28):9764-73. doi: 10.1021/ja102367x.
In this paper, the characterization of a protic ionic liquid, diethylmethylammonium trifluoromethanesulfonate ([dema][TfO]), as a proton conductor for a fuel cell and the fabrication of a membrane-type fuel cell system using [dema][TfO] under nonhumidified conditions at intermediate temperatures are described in detail. In terms of physicochemical and electrochemical properties, [dema][TfO] exhibits high activity for fuel cell electrode reactions (i.e., the hydrogen oxidation reaction (HOR) and oxygen reduction reaction (ORR)) at a Pt electrode, and the open circuit voltage (OCV) of a liquid fuel cell is 1.03 V at 150 degrees C, as has reported in ref 27. However, diethylmethylammonium bis(trifluoromethane sulfonyl)amide ([dema][NTf(2)]) has relatively low HOR and ORR activity, and thus, the OCV is ca. 0.7 V, although [dema][NTf(2)] and [dema][TfO] have an identical cation ([dema]) and similar thermal and bulk-transport properties. Proton conduction occurs mainly via the vehicle mechanism in [dema][TfO] and the proton transference number (t(+)) is 0.5-0.6. This relatively low t(+) appears to be more disadvantageous for a proton conductor than for other electrolytes such as hydrated sulfonated polymer electrolyte membranes (t(+) = 1.0). However, fast proton-exchange reactions occur between ammonium cations and amines in a model compound. This indicates that the proton-exchange mechanism contributes to the fuel cell system under operation, where deprotonated amines are continuously generated by the cathodic reaction, and that polarization of the cell is avoided. Six-membered sulfonated polyimides in the diethylmethylammonium form exhibit excellent compatibility with [dema][TfO]. The composite membranes can be obtained up to a [dema][TfO] content of 80 wt % and exhibit good thermal stability, high ionic conductivity, and mechanical strength and gas permeation comparable to those of hydrated Nafion. H(2)/O(2) fuel cells prepared using the composite membranes can successfully operate at temperatures from 30 to 140 degrees C under nonhumidified conditions, and a current density of 250 mA cm(-2) is achieved at 120 degrees C. The protic ionic liquid and its composite membrane are a possible candidate for an electrolyte of a H(2)/O(2) fuel cell that operates under nonhumidified conditions.
本文详细描述了质子离子液体二乙基甲基铵三氟甲磺酸酯([dema][TfO])作为质子导体在非加湿条件下在中温下用于燃料电池的特性,以及使用[dema][TfO]制造膜式燃料电池系统。在物理化学和电化学性质方面,[dema][TfO]在 Pt 电极上对燃料电池电极反应(即氢气氧化反应(HOR)和氧气还原反应(ORR))具有高活性,并且在 150°C 时液体燃料电池的开路电压(OCV)为 1.03V,如参考文献 27 所述。然而,二乙基甲基铵双(三氟甲烷磺酰基)酰胺([dema][NTf(2)])的 HOR 和 ORR 活性相对较低,因此 OCV 约为 0.7V,尽管 [dema][NTf(2)] 和 [dema][TfO]具有相同的阳离子([dema])和相似的热和体传输特性。质子传导主要通过 [dema][TfO]中的载体机制发生,质子迁移数(t(+))为 0.5-0.6。对于质子导体而言,这种相对较低的 t(+)似乎比其他电解质(例如水合磺化聚合物电解质膜,t(+)=1.0)更不利。然而,在模型化合物中,铵阳离子和胺之间会发生快速质子交换反应。这表明质子交换机制有助于运行中的燃料电池系统,其中通过阴极反应连续产生去质子化的胺,并且避免了电池的极化。二乙基甲基铵形式的六元磺化聚酰亚胺与[dema][TfO]具有极好的相容性。可以获得高达 80wt%[dema][TfO]含量的复合膜,并表现出良好的热稳定性,高离子电导率和机械强度以及与水合 Nafion 相当的气体渗透性。使用复合膜制备的 H2/O2 燃料电池可以在非加湿条件下成功地在 30 至 140°C 的温度下运行,并且在 120°C 时达到 250mA cm(-2)的电流密度。质子离子液体及其复合膜是在非加湿条件下运行的 H2/O2 燃料电池电解质的可能候选物。