Stable complete seawater electrolysis by using interfacial chloride ion blocking layer on catalyst surface

被引:155
作者
Jadhav, Amol R. [1 ]
Kumar, Ashwani [1 ,2 ]
Lee, Jinju [1 ,2 ]
Yang, Taehun [1 ,2 ]
Na, Siyoung [2 ]
Lee, Jinsun [1 ,2 ]
Luo, Yongguang [1 ,2 ]
Liu, Xinghui [1 ,2 ]
Hwang, Yosep [1 ,2 ]
Liu, Yang [1 ,2 ]
Lee, Hyoyoung [1 ,2 ,3 ,4 ]
机构
[1] Sungkyunkwan Univ, Ctr Integrated Nanostruct Phys CINAP, Inst Basic Sci IBS, Suwon 16419, South Korea
[2] Sungkyunkwan Univ, Dept Chem, Suwon 16419, South Korea
[3] Sungkyunkwan Univ, Dept Biophys, Suwon 16419, South Korea
[4] Sungkyunkwan Univ, Creat Res Inst, Suwon 16419, South Korea
基金
新加坡国家研究基金会;
关键词
HYDROGEN EVOLUTION; COBALT HYDROXIDE; HIGHLY EFFICIENT; OXYGEN EVOLUTION; NIFE-LDH; WATER; GRAPHENE; ELECTROCATALYST; OPPORTUNITIES; FABRICATION;
D O I
10.1039/d0ta08543j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Seawater is the most plentiful natural resource we have on earth and new research is looking at seawater as an alternative to freshwater for hydrogen production by electrolysis. However, the selective electrochemical anodic oxygen evolution reaction from seawater is challenging because of the competitive chloride oxidation reaction as well as anodic corrosion. Here we report an FeOOH deposited beta-Ni-Co hydroxide as a new active material with an outer graphene oxide layer, which works effectively for selective overall alkaline natural seawater splitting, which requires very low cell voltages of 1.57 and 2.02 V to reach current densities of 20 mA cm(-2) and 1000 mA cm(-2), respectively, at 27 degrees C. Importantly, this electrolyzer shows exceptional stability for more than 378 h at a current density of 1 A cm(-2). This discovery can be generalized with other reported unstable OER/HER seawater splitting electrocatalysts, which can significantly progress the expansion of seawater electrolysis for extensive hydrogen production.
引用
收藏
页码:24501 / 24514
页数:14
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