Improvement of the selectivity of the electrochemical conversion of CO2 to hydrocarbons using cupreous electrodes with in-situ oxidation by oxygen

被引:37
作者
Engelbrecht, Andreas [1 ]
Haemmerle, Martin [1 ]
Moos, Ralf [1 ]
Fleischer, Maximilian [2 ]
Schmid, Guenter [3 ]
机构
[1] Univ Bayreuth, Fac Engn Sci, Dept Funct Mat, Univ Str 30, D-95440 Bayreuth, Germany
[2] Siemens AG Munchen Perlach, Otto Hahn Ring 6, D-81739 Munich, Germany
[3] Siemens AG Erlangen Sud, Gunther Scharowsky Str 1, D-91052 Erlangen, Germany
关键词
electrochemical reduction; carbon dioxide; copper oxide; ethylene; hydrocarbons; selectivity; COPPER SINGLE-CRYSTAL; CARBON-DIOXIDE; PULSED ELECTROREDUCTION; POLYCRYSTALLINE COPPER; REDUCTION; ETHYLENE; SURFACE; CATALYSTS; CU(100);
D O I
10.1016/j.electacta.2016.12.059
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
It is still a challenge to find catalysts for the selective electrochemical reduction of CO2 to value added products. We present a new method for the in-situ modification of a copper catalyst by adding oxygen to the reactant gas. With an appropriate process procedure consisting of a sequence of electrolysis and purge steps, a Cu2O layer was formed during the purge steps. When it was reduced again during the next electrolysis step, Cu+ species remained stable on the surface and let to a higher faradaic efficiency for C2H4 formation and even a lower onset potential for CO2 reduction in general. This effect was observed for a wide range of O-2 content from 10 % to 60 % in the reactant gas. In comparison to electrolysis with pure CO2, formation of methane was largely suppressed. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:642 / 648
页数:7
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