On the Electrochemical CO2 Reduction at Copper Sheet Electrodes with Enhanced Long-Term Stability by Pulsed Electrolysis

被引:69
作者
Engelbrecht, Andreas [1 ]
Uhlig, Conrad [1 ,4 ]
Stark, Oliver [1 ,5 ]
Haemmerle, Martin [1 ]
Schmid, Guenter [2 ]
Magori, Erhard [3 ]
Wiesner-Fleischer, Kerstin [3 ]
Fleischer, Maximilian [3 ]
Moos, Ralf [1 ]
机构
[1] Univ Bayreuth, Fac Engn Sci, Ctr Energy Technol ZET, Dept Funct Mat, D-95440 Bayreuth, Germany
[2] Siemens AG Erlangen Sud, D-91052 Erlangen, Germany
[3] Siemens AG Munchen Perlach, D-81739 Munich, Germany
[4] Die Patenterie GbR, Leibnizstr 6, D-95447 Bayreuth, Germany
[5] Hof Univ, Inst Water & Energy Management, Alfons Goppel Pl 1, D-95028 Hof, Germany
关键词
CARBON-DIOXIDE; CU ELECTRODE; ETHYLENE; ELECTROREDUCTION; SURFACE; HYDROCARBONS; SELECTIVITY; CONVERSION; OXIDATION; MONOXIDE;
D O I
10.1149/2.0091815jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
We report on the long-term stability of the electrochemical reduction of CO2 at copper sheet electrodes by continuously applying rectangular, pulsed voltage cycles in series. Each pulse cycle consisted of an anodic and a cathodic voltage level. The parameters of the pulse cycle were systematically modified: cathodic (-1.5...-1.8 V) and anodic voltage levels (-0.88...+0.15 V), and ratio of anodic to cathodic pulse duration (5 s: 5 s... 5 s: 500 s). The electrolysis runs were conducted in a divided H-cell. Volatile reaction products (CO, CH4, C2H4, H-2) were analyzed with a gas chromatograph in intervals of 7.3 min. We achieved fairly stable faradaic efficiencies (FE) for hydrocarbon formation in the range of 20 to 35% FE for C2H4 and 20 to 50% FE for CH4 during 16 h of electrolysis and a remarkable suppression of hydrogen evolution reaction (HER) down to 10% FE. Additionally, we show data of two long-term electrolysis runs of 85 h and 95 h duration, respectively. Even for this prolonged electrolysis times, an outstanding, fairly constant suppression of HER and a high efficiency for the formation of carbon containing gaseous products (CO, CH4, C2H4) was achieved. (C) The Author(s) 2018. Published by ECS.
引用
收藏
页码:J3059 / J3068
页数:10
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