Ren Yongwen, Fan Faying, Zhang Yaojian, Chen Lin, Wang Zhe, Li Jiedong, Zhao Jingwen, Tang Bo, Cui Guanglei
Qingdao Industrial Energy Storage Research Institute, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao, 266101, China.
Shandong Energy Institute, Qingdao, 266101, China.
Adv Sci (Weinh). 2024 Jul;11(25):e2401702. doi: 10.1002/advs.202401702. Epub 2024 Apr 3.
Direct seawater splitting (DSS) offers an aspirational route toward green hydrogen (H) production but remains challenging when operating in a practically continuous manner, mainly due to the difficulty in establishing the water supply-consumption balance under the interference from impurity ions. A DSS system is reported for continuous ampere-level H production by coupling a dual-cation exchange membrane (CEM) three-compartment architecture with a circulatory electrolyte design. Monovalent-selective CEMs decouple the transmembrane water migration from interferences of Mg, Ca, and Cl ions while maintaining ionic neutrality during electrolysis; the self-loop concentrated alkaline electrolyte ensures the constant gradient of water chemical potential, allowing a specific water supply-consumption balance relationship in a seawater-electrolyte-H sequence to be built among an expanded current range. Even paired with commercialized Ni foams, this electrolyzer (model size: 2 × 2 cm) continuously produces H from flowing seawater with a rate of 7.5 mL min at an industrially relevant current of 1.0 A over 100 h. More importantly, the energy consumption can be further reduced by coupling more efficient NiMo/NiFe foams (≈6.2 kWh Nm H at 1.0 A), demonstrating the potential to further optimize the continuous DSS electrolyzer for practical applications.
直接海水分解(DSS)为绿色氢气(H₂)生产提供了一条理想途径,但在实际连续运行时仍面临挑战,主要原因是在杂质离子干扰下难以建立水的供需平衡。本文报道了一种DSS系统,该系统通过将双阳离子交换膜(CEM)三室结构与循环电解质设计相结合,实现了连续安培级别的H₂生产。单价选择性CEMs在电解过程中保持离子中性的同时,将跨膜水迁移与Mg²⁺、Ca²⁺和Cl⁻离子的干扰解耦;自循环浓缩碱性电解质确保了水化学势的恒定梯度,从而在较宽的电流范围内,在海水-电解质-H₂序列中建立了特定的水供需平衡关系。即使与商业化的泡沫镍配对,这种电解槽(模型尺寸:2×2 cm)在1.0 A的工业相关电流下,能从流动海水中以7.5 mL min⁻¹的速率连续产生H₂,持续超过100小时。更重要的是,通过耦合更高效的NiMo/NiFe泡沫(在1.0 A时≈6.2 kWh Nm⁻³ H₂),能耗可进一步降低,这表明进一步优化连续DSS电解槽以用于实际应用具有潜力。