摘要

A series of polystyrene-block-poly(ethylene-ran-butylene)-block-polystyrene (SEBS)-based anion exchange membranes (AEMs) were synthesized via chloromethylation of SEBS followed by quaternization with trimethylamine (TMA). SEBS-based AEMs functionalized with TMA(+) cations exhibited a hydroxide ion conductivity of 136 mS/cm at 70 degrees C. This membrane exhibited a phase-separated morphology with wide and interconnected ionic channels as observed by atomic force microscopy. Poly (phenylene oxide) (PPO)-based AEMs with quaternary benzyl-trimethylammonium (TMA(+)) and quaternary benzyl-tris(2,4,6-trimethoxyphenyl) phosphonium (TTMPP+) and PPO-based AEMs with hexyl pendant chains were also synthesized and evaluated as binders in AMFC electrodes. PPO-based AEMs functionalized with TTMPP+ demonstrated the best ex situ alkaline stability, losing only 9% of their ion-exchange-capacity after 30 days in 1M KOH (at 60 degrees C). The best in situ stability was achieved by SEBS-based MEAs (as membrane and as binder in the electrodes); The peak power density dropped approx. 35% after holding the cell at a constant voltage of 0.55V for 12 hours. Fuel cell performance with SEBS-based AEMs resulted in peak power densities of 300 mW/cm(2) at 70 degrees C. The optimum performance was obtained with MEAs made with SEBS-based AEMs and PPO-based ionomers containing a hexyl pendant chain.

  • 出版日期2017