电解
海水
电解质
高压电解
电解水
制氢
化学工程
化学
材料科学
氢
无机化学
工艺工程
电极
有机化学
物理化学
工程类
地质学
海洋学
作者
Yongwen Ren,Faying Fan,Yaojian Zhang,Lin Chen,Zhe Wang,Jiedong Li,Jingwen Zhao,Bo Tang,Guanglei Cui
出处
期刊:Advanced Science
[Wiley]
日期:2024-04-03
卷期号:11 (25): e2401702-e2401702
被引量:37
标识
DOI:10.1002/advs.202401702
摘要
Abstract Direct seawater splitting (DSS) offers an aspirational route toward green hydrogen (H2) 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 H2 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 Mg2+, Ca2+, 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–H2 sequence to be built among an expanded current range. Even paired with commercialized Ni foams, this electrolyzer (model size: 2 × 2 cm2) continuously produces H2 from flowing seawater with a rate of 7.5 mL min−1 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−3 H2 at 1.0 A), demonstrating the potential to further optimize the continuous DSS electrolyzer for practical applications.
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