A membrane-based seawater electrolyser for hydrogen generation

被引:644
作者
Xie, Heping [1 ,2 ]
Zhao, Zhiyu [2 ]
Liu, Tao [2 ]
Wu, Yifan [2 ]
Lan, Cheng [2 ]
Jiang, Wenchuan [2 ]
Zhu, Liangyu [3 ]
Wang, Yunpeng [4 ]
Yang, Dongsheng [5 ]
Shao, Zongping [6 ,7 ]
机构
[1] Shenzhen Univ, Coll Civil & Transportat Engn, Inst Deep Earth Sci & Green Energy, Guangdong Prov Key Lab Deep Earth Sci & Geotherma, Shenzhen, Peoples R China
[2] Sichuan Univ, Inst New Energy & Low Carbon Technol, Chengdu, Peoples R China
[3] Southwest Petr Univ, Petroteum Engn Sch, Chengdu, Peoples R China
[4] Sichuan Univ, Sch Chem Engn, Chengdu, Peoples R China
[5] Sichuan Univ, Coll Polymer Sci & Engn, Chengdu, Peoples R China
[6] Nanjing Tech Univ, Coll Chem Engn, State Key Lab Mat Oriented Chem Engn, Nanjing, Peoples R China
[7] Curtin Univ, WA Sch Mines Minerals Energy & Chem Engn, Perth, WA, Australia
基金
中国国家自然科学基金;
关键词
MASS-TRANSPORT; DESALINATION;
D O I
10.1038/s41586-022-05379-5
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Electrochemical saline water electrolysis using renewable energy as input is a highly desirable and sustainable method for the mass production of green hydrogen(1-7); however, its practical viability is seriously challenged by insufficient durability because of the electrode side reactions and corrosion issues arising from the complex components of seawater. Although catalyst engineering using polyanion coatings to suppress corrosion by chloride ions or creating highly selective electrocatalysts has been extensively exploited with modest success, it is still far from satisfactory for practical applications(8-14). Indirect seawater splitting by using a pre-desalination process can avoid side-reaction and corrosion problems(15-21), but it requires additional energy input, making it economically less attractive. In addition, the independent bulky desalination system makes seawater electrolysis systems less flexible in terms of size. Here we propose a direct seawater electrolysis method for hydrogen production that radically addresses the side-reaction and corrosion problems. A demonstration system was stably operated at a current density of 250milliamperes per square centimetre for over 3,200hours under practical application conditions without failure. This strategy realizes efficient, size-flexible and scalable direct seawater electrolysis in a way similar to freshwater splitting without a notable increase in operation cost, and has high potential for practical application. Importantly, this configuration and mechanism promises further applications in simultaneous water-based effluent treatment and resource recovery and hydrogen generation in one step.
引用
收藏
页码:673 / +
页数:20
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