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 • C. This membrane exhibited a phaseseparated 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 • 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 • C. Anion exchange membranes (AEMs) are a promising technology for alkaline membrane fuel cells (AMFCs), 1-6 redox flow batteries (RFBs), 7-13 alkaline water electrolyzers (AWEs) [14][15][16] and reverse electrodialysis (RED) cells. 17,18 The AEMs commonly reported in peer reviewed papers mostly contain quaternary ammonium fixed cation groups, mainly in the form of benzyl trimethylammonium cations.14,19-40 However, it has been shown that quaternary ammonium-based AEMs are sensitive toward Hofmann elimination 20,41 and direct nucleophilic elimination reactions 42,43 that result in loss of ion exchange capacity (IEC) and ionic conductivity. To resolve the stability problem inherent to quaternary-ammonium-group-containing AEMs, several alternative cations, including imidazolium, 41,44,45 benzimidazolium, 3,45,46 guanidinium, 15,47,48 phosphonium 8,9,49 and metal cations 50,51 have been proposed and investigated. Phosphonium-based AEMs were investigated by Gu et al. 52 Gu et al. attached benzyl-tris(2,4,6-trimethoxyphenyl) phosphonium (TTMPP + ) onto polysulfone backbone to make AEMs, and found them to be alkaline stable; There was no ionic conductivity fade after immersion in 1M KOH for 30 days at room temperature. The bulky phosphonium-based AEMs remained stable in alkali because of the steric hindrance effect that protects the core phosphorus atom and the α-carbons against hydroxide ion attack. There is no possibility of β-elimination reaction because of the lack of hydrogen atoms in β-carbons. However, very few researchers have investigated in situ stability of bulky phosphorus-based AEMs. It is essential to correlate the ex situ stability results obtained in immersion alkaline stability tests with in situ stability in a functional H 2 /O 2 fuel cell.Hibbs 53 has shown that poly(phenylene)-bas...