Decoupling hydrogen and oxygen evolution during electrolytic water splitting using an electron-coupled-proton buffer

被引:496
作者
Symes, Mark D. [1 ]
Cronin, Leroy [1 ]
机构
[1] Univ Glasgow, WestCHEM, Sch Chem, Glasgow G12 8QQ, Lanark, Scotland
基金
英国工程与自然科学研究理事会;
关键词
KEGGIN-TYPE; ENERGY; DEGRADATION; RESISTANCE; CATALYSTS; ACID; PULP; H-2; NI;
D O I
10.1038/nchem.1621
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hydrogen is essential to several key industrial processes and could play a major role as an energy carrier in a future 'hydrogen economy'. Although the majority of the world's hydrogen supply currently comes from the reformation of fossil fuels, its generation from water using renewables-generated power could provide a hydrogen source without increasing atmospheric CO2 levels. Conventional water electrolysis produces H-2 and O-2 simultaneously, such that these gases must be generated in separate spaces to prevent their mixing. Herein, using the polyoxometalate H3PMo12O40, we introduce the concept of the electron-coupled-proton buffer (ECPB), whereby O-2 and H-2 can be produced at separate times during water electrolysis. This could have advantages in preventing gas mixing in the headspaces of high-pressure electrolysis cells, with implications for safety and electrolyser degradation. Furthermore, we demonstrate that temporally separated O-2 and H-2 production allows greater flexibility regarding the membranes and electrodes that can be used in water-splitting cells.
引用
收藏
页码:403 / 409
页数:7
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