电解质
材料科学
法拉第效率
催化作用
阴极
无机化学
甲醇
混合(物理)
化学工程
选择性
电极
化学
有机化学
物理化学
工程类
物理
量子力学
作者
Chuan Xia,Peng Zhu,Qiu Jiang,Ying Pan,Wentao Liang,Eli Stavitski,Husam N. Alshareef,Haotian Wang
出处
期刊:Nature Energy
[Springer Nature]
日期:2019-09-02
卷期号:4 (9): 776-785
被引量:540
标识
DOI:10.1038/s41560-019-0451-x
摘要
Electrocatalytic CO2 reduction is often carried out in a solution electrolyte such as KHCO3(aq), which allows for ion conduction between electrodes. Therefore, liquid products that form are in a mixture with the dissolved salts, requiring energy-intensive downstream separation. Here, we report continuous electrocatalytic conversion of CO2 to pure liquid fuel solutions in cells that utilize solid electrolytes, where electrochemically generated cations (such as H+) and anions (such as HCOO−) are combined to form pure product solutions without mixing with other ions. Using a HCOOH-selective (Faradaic efficiencies > 90%) and easily scaled Bi catalyst at the cathode, we demonstrate production of pure HCOOH solutions with concentrations up to 12 M. We also show 100 h continuous and stable generation of 0.1 M HCOOH with negligible degradation in selectivity and activity. Production of other electrolyte-free C2+ liquid oxygenate solutions, including acetic acid, ethanol and n-propanol, are also demonstrated using a Cu catalyst. Finally, we show that our CO2 reduction cell with solid electrolytes can be modified to suit other, more complex practical applications. Liquid products from electrocatalytic CO2 reduction are often mixed with additional solutes in the electrolyte, meaning that downstream separation is required. Here, the authors design cells that use solid electrolytes to generate flows of CO2-derived liquid fuels with high concentrations that are free of extraneous ions.
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