The call for cleaner energy sources motivates the development
of
anion exchange membrane fuel cells (AEMFC), which offer potential
for electricity production using carbon-neutral fuels. However, the
focus on biopolymer-based ion exchange membranes (IEM) remains relatively
low, despite their strong potential for cost reduction and competitive
performance. Studies have demonstrated the fabrication of high-performing
synthetic AEMs using semi-interpenetrating polymer networks (SIPNs)
showcasing improved mechanical stability and electrochemical properties,
offering a pathway for cost-effective AEMFC adoption. In this study,
a biopolymer SIPN of cellulose acetate (CA) nanofibers and cross-linked
chitosan (CS) was fabricated into AEM. FTIR and Raman spectroscopy
confirmed CS addition, its cross-linking to form the SIPN, and subsequent
functionalization to obtain the AEM. Thermogravimetric analysis of
fabricated AEM revealed thermal stability well within AEMFC operating
conditions, and the formation of SIPN structure increased tensile
strength by 95%. Deacetylation of cellulose diacetate (CDA) nanofibers
into cellulose monoacetate (CMA) and cellulose improved the ion exchange
capacity (IEC) by up to 12% due to conversion of the acetyl group
into hydroxyl groups acting as active sites for functionalization.
Ionic conductivities peaked at 60 °C of 21 mS cm−1 for a 150 μm cellulose-chitosan SIPN AEM. No appreciable change
in swelling was observed among membranes of the same components with
differing IEC, indicating the SIPN’s ability to restrict membrane
expansion despite increased presence of hydrophilic groups. Desirable
mechanical integrity was observed with reduced swelling in SIPN AEMs
compared to CA film AEMs of the same thickness. These properties demonstrate
the success of our fabrication method for a dimensionally stable biopolymer
AEM with controlled swelling and appreciable ion transport capabilities
that are suitable for fuel cell applications.