A Zero-Gap Electrolyzer Enables Supporting Electrolyte-Free Seawater Splitting for Energy-Saving Hydrogen Production

被引:0
|
作者
Ren, Yongwen [1 ,2 ,3 ]
Fan, Faying [1 ,2 ,3 ]
Zhang, Shu [1 ,2 ,3 ]
Liu, Zhaohan [4 ]
Zhang, Yaojian [1 ,2 ,3 ]
Sun, Fu [1 ,2 ,3 ]
Li, Jiedong [1 ,2 ,3 ]
Chen, Lin [1 ,2 ,3 ]
Wang, Zhe [1 ,2 ,3 ]
Zhao, Jingwen [1 ,2 ,3 ]
Qiu, Jieshan [5 ]
Cui, Guanglei [1 ,2 ,3 ,6 ]
机构
[1] Chinese Acad Sci, Qingdao Ind Energy Storage Res Inst, Qingdao Inst Bioenergy & Bioproc Technol, Qingdao 266101, Peoples R China
[2] Shandong Energy Inst, Qingdao 266101, Peoples R China
[3] Qingdao New Energy Shandong Lab, Qingdao 266101, Peoples R China
[4] Japan Adv Inst Sci & Technol, Grad Sch Adv Sci & Technol, Nomi, Ishikawa 9231292, Japan
[5] Beijing Univ Chem Technol, Coll Chem Engn, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[6] Univ Chinese Acad Sci, Sch Future Technol, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
direct seawater splitting; zero-gap electrolyzer; green hydrogen production; supporting electrolytes; bipolar membrane; WATER DISSOCIATION; OXIDATION; MEMBRANES; CATALYST; DESIGN;
D O I
10.1002/anie.202422840
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Membrane-assisted direct seawater splitting (DSS) technologies are actively studied as a promising route to produce green hydrogen (H2), whereas the indispensable use of supporting electrolytes that help to extract water and provide electrochemically-accelerated reaction media results in a severe energy penalty, consuming up to 12.5 % of energy input when using a typical KOH electrolyte. We bypass this issue by designing a zero-gap electrolyzer configuration based on the integration of cation exchange membrane and bipolar membrane assemblies, which protects stable DSS operation against the precipitates and corrosion in the absence of additional supporting electrolytes. The heterolytic water dissociation function of the bipolar membrane in situ creates an asymmetric acidic-alkaline environment, kinetically facilitating H2 and O2 evolution reactions. When working in natural seawater without any chemical inputs, this zero-gap electrolyzer sustains nearly 100 % Faradaic efficiency toward H2 for 120 h at a current density of 100 mA cm-2. With the high-integrity merit, our electrolyzer can be facilely scaled up into practical cell stacks with significantly increased active area and promising prospects for volume/space-sensitive application scenarios. This electrolyzer concept opens an underexplored design space for energy-saving H2 production from low-grade saline water sources, being complementary to, and potentially competitive with the pre-purification Schemes.
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页数:10
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