The piperidinium-based AEM was able to maintain its ca. 90% of its initial IEC after immersion into 1M KOH at 80 ºC for 30 days. Such piperidinium-based AEMs showed higher alkaline stability than benzyl-trimethylammonium-based AEM (ca. 20% degradation in 1M KOH at 60 ºC for 30 days) [3]. The improved alkaline stability was mainly attributed to the avoidance of attaching quaternary ammonium onto benzylic position. The planar structure of piperidinium-based cation slows down the β-elimination phenomenon. Also, there is no ether linkage with the polymer backbone and hence, the stability of polymer backbone is superior. The chloride ion conductivity of the piperidinium-based AEM was 65 mS/cm at 80 ºC under an IEC of 2.26 mmol/g. An AEMFC was assembled using our piperidinium-based AEM with Pt/C catalysts used for both anode and cathode. A peak power density of 700 mW/cm2 with 2 A/cm2 current density was obtained at 70 ºC without any backpressure.
References
[1] C.G. Arges, L. Wang, J. Parrondo, V. Ramani, Journal of The Electrochemical Society, 160 (2013) F1258-F1274.
[2] S. Chempath, J.M. Boncella, L.R. Pratt, N. Henson, B.S. Pivovar, The Journal of Physical Chemistry C, 114 (2010) 11977-11983.
[3] Z. Wang, J. Parrondo, V. Ramani, Journal of The Electrochemical Society, 164 (2017) F1216-F1225.
