Co-electrolysis of CO2 and H2O: From electrode reactions to cell-level development

被引:38
|
作者
Herranz, Juan [1 ]
Patru, Alexandra [1 ]
Fabbri, Emiliana [1 ]
Schmidt, Thomas J. [1 ,2 ]
机构
[1] Paul Scherrer Inst, Electrochem Lab, CH-5232 Villigen, Switzerland
[2] Swiss Fed Inst Technol, Lab Phys Chem, CH-8093 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
OXYGEN EVOLUTION REACTION; CARBON-DIOXIDE; ELECTROCHEMICAL REDUCTION; WATER OXIDATION; CATALYST; DESIGN; SYNGAS; SELECTIVITY; EFFICIENT; CATHODE;
D O I
10.1016/j.coelec.2020.05.004
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
The electroreduction of CO2 into value-added products (e.g. CO) constitutes an excellent means of decreasing this greenhouse gas emissions, but limited efforts have been devoted to the implementation of this reaction within the so-called co-electrolysis cells operating at process-relevant currents >> 100 mA.cm(geom)(-2). Reaching such performances shall require a combination of gas-fed reactants and the corresponding diffusion electrodes, along with ion-exchange membranes and ionomers that set the operative pH at the cells' cathode and anode. The latter constitutes a key design parameter that must be combined with the need to minimize the crossover of reaction products and/or (bi)carbonate anions from the cathode to the anode, whereby their reoxidation to carbon dioxide leads to a decrease in the device's net CO2 consumption.
引用
收藏
页码:89 / 95
页数:7
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