Phosphoric Acid Diethylmethylammonium Trifluoromethanesulfonate-Based Electrolytes for Nonhumidified Intermediate Temperature Fuel Cells

Abstract

The present study reports a new series of electrolytes for nonhumidified intermediate temperature fuel cells (IT-FCs). This series of new mixed electrolytes, composed of phosphoric acid (PA) and diethylmethylammonium trifluoromethanesulfonate ([dema]­[TfO]), was designed as nonhumidified IT-FC electrolytes. The mixed electrolytes show a higher thermal stability than pure PA, which is dehydrated at ITs. The thermal stability of the mixed electrolytes could be explained by the interaction between the triflate group in [dema]­[TfO] and PA, as indicated by Fourier transform infrared and proton nuclear magnetic resonance (1H NMR) spectroscopies. On the other hand, the ionic conductivity and proton transference number of the mixed electrolytes were similar to those of the pure PA. However, the oxygen reduction reaction (ORR) activity of a platinum catalyst is significantly enhanced in the mixed electrolytes, which was due to the several orders of magnitude increase in oxygen solubility by the addition of [dema]­[TfO] to PA. Specifically, for the equimolar fraction mixed electrolyte, the diffusion coefficient and the solubility of oxygen were ca. 1.47 × 10–5 cm2 s–1 and ca. 1.28 mmol dm–3 at 150 °C, respectively. The addition of [dema]­[TfO] to PA could significantly enhance the ORR activity. Therefore, the PA_[dema]­[TfO] mixed electrolyte can be one of the solutions to develop nonhumidified intermediate FC electrolytes