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Alkaline water electrolysis is one of the primary drivers of hydrogen energy development, and anion exchange membranes (AEMs) play a dual role in ensuring both conductivity and safety. However, traditional polymer AEMs have a wide pore size distribution and poor chemical stability, making it difficult to achieve a long-term balance between conductivity and safety of the water electrolysis system. Here, we select inorganic two-dimensional multilayer graphene oxide (GO) membranes as AEMs, using carboxylated wrinkled graphene (WG) and ethylenediamine (EDA) to create a cation-modified porous EDA-WG/GO (E-W/G) composite membrane with a 3 nm pore size. The enlarged channel size and enhanced hydrophilicity improve OH − permeability compared to the pristine GO membrane, while the strengthened hydration layer acts as a barrier to hydrophobic gases for O 2 /H 2 separation. The results show that the prepared E-W/G membrane exhibits superior current density (600 mA cm −2 ) and gas impermeability (gas purity 99.99%) compared to the commercial Fumasep FAA-3-50 membrane (590 mA cm −2 and 99.81%, respectively). Furthermore, after continuous testing for 168 h in high-temperature and alkaline environments, the E-W/G membrane maintained conductivity comparable to its initial state and showed enhanced gas impermeability. Our strategy provides new insights into the design of high-performance AEMs and is expected to contribute to the advancement of the hydrogen energy industry. 3 nm-sized porous EDA-WG/GO AEMs for highly effective and stable water electrolysis. • Developed a strategy for constructing 3 nm-sized porous graphene membranes • The 3 nm structures enhanced the OH − permeability • The improved membrane hydrophily effective isolation of gas penetration • GO-based AEMs could present a stable conduction and gas isolation properties
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Liu et al. (2024) studied this question.
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