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Demonstrates enhanced performance of self-crosslinked anion exchange membranes, suggesting improved fuel cell efficiency.
Anion exchange membrane fuel cells are currently limited by the lack of durable, high‐performance anion exchange membranes (AEMs). Herein, we develop a pH‐dependent self‐crosslinking strategy to fabricate large‐area AEMs without external crosslinking agents that leverages the protonation of a precursor polymer under acidic conditions (pH <7) to maintain solubility, while an alkaline environment (pH >7) induces deprotonation and triggers a Menshutkin reaction for self‐crosslinking. The resulting self‐crosslinked network in the AEMs (OH − form) effectively restricts polymer chain mobility and enhances interchain entanglement, leading to low water uptake (28.6%), minimal swelling (10.2%), high mechanical strength (70.2 MPa), and good alkaline stability over 5000 h (only 3.1% conductivity loss). Furthermore, the membrane demonstrates high hydroxide conductivity and reduced H 2 permeability, enabling high‐performance fuel cells operation with a peak power density of 2.10 W cm −2 and extended durability under harsh conditions (0.6 A cm −2 , 80°C).
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Yuan et al. (2026) studied this question.
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