法拉第效率
一氧化碳
电解质
电解
碳纤维
法拉第电流
水溶液
电极
化学工程
电解水
化学
无机化学
催化作用
分析化学(期刊)
材料科学
电极电位
有机化学
复合材料
物理化学
复合数
工程类
作者
Matthew Jouny,Wesley Luc,Feng Jiao
出处
期刊:Nature Catalysis
[Springer Nature]
日期:2018-08-17
卷期号:1 (10): 748-755
被引量:490
标识
DOI:10.1038/s41929-018-0133-2
摘要
Carbon monoxide electrolysis has previously been reported to yield enhanced multi-carbon (C2+) Faradaic efficiencies of up to ~55%, but only at low reaction rates. This is due to the low solubility of CO in aqueous electrolytes and operation in batch-type reactors. Here, we present a high-performance CO flow electrolyser with a well controlled electrode–electrolyte interface that can reach total current densities of up to 1 A cm–2, together with improved C2+ selectivities. Computational transport modelling and isotopic C18O reduction experiments suggest that the enhanced activity is due to a higher surface pH under CO reduction conditions, which facilitates the production of acetate. At optimal operating conditions, we achieve a C2+ Faradaic efficiency of ~91% with a C2+ partial current density over 630 mA cm–2. Further investigations show that maintaining an efficient triple-phase boundary at the electrode–electrolyte interface is the most critical challenge in achieving a stable CO/CO2 electrolysis process at high rates. The low solubility of CO in aqueous electrolytes limits the implementation of CO electrolysers, since low current densities are typically achieved despite the fact that they deliver rather high Faradaic efficiencies to multi-carbon products. Now, Jiao and co-workers report a CO flow electrolyser with a well-controlled electrode–electrolyte interface that can achieve multi-carbon Faradaic efficiencies of 91% with a partial current density of 630 mA cm–2.
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