Alkaline
anion exchange membranes (AEMs) were developed from a
series of persubstituted imidazolium cations with varying alkyl chains
(Im-nC, nC = (CH2)
n−1CH3; n = 4, 12, and 16) tethered on poly(vinylbenzyl
chloride-co-acrylonitrile) (PVC-co-AN) to prepare a comb-shaped polymer membrane (M1-nC) and a cross-linked polymer membrane from polyimidazolium cations
and PVC-co-AN (M3). The PVC-co-AN
polymer backbone shows high stability after curing, and the water
uptake and swelling ratio are controlled by varying the alkyl chain
length in M1-nC even with temperature variation.
Results show that M1-16C retains the highest ion exchange capacity
(IEC) of 95% among the M1-nC series of membranes
after exposure to 1 M KOH solution at 80 °C for 30 days. However,
the longer alkyl chains hindered the interconnected ion channels limiting
the hydrophobic/hydrophilic phase separation and the hydroxide ion
conductivity. Meanwhile, M3 exhibits a distinct microphase-separated
morphology and a high ionic conductivity of 54.5 mS/cm for a 2.02
IEC with high stability to retain an IEC of 97% after storage in 1
M KOH solution at 80 °C for 30 days. In addition, all the AEMs
exhibit high oxidation stability and retain >96% weight after immersion
into 4 ppm Fenton’s reagent at 80 °C. Moreover, the flexible
solid-state zinc–air batteries comprising an M3 membrane displayed
a peak power density of 165 mW cm–2 and superior
cycling stability (30 h at 10 mA cm–2) demonstrating
very promising applications in solid-state flexible rechargeable Zn–air
batteries.