合成气
人工光合作用
电解
工艺工程
环境科学
化学
可再生能源
电解水
材料科学
制浆造纸工业
废物管理
化学工程
氢
工程类
有机化学
电极
催化作用
电气工程
物理化学
电解质
光催化
作者
Thomas Haas,Ralf Krause,Rainer Weber,Martin Demler,Guenter Schmid
标识
DOI:10.1038/s41929-017-0005-1
摘要
Solar-powered electrochemical reduction of CO2 and H2O to syngas, followed by fermentation, could lead to sustainable production of useful chemicals. However, due to insufficient electric current densities and instabilities of current CO2-to-CO electrolysers, a practical, scalable artificial photosynthesis remains a major challenge. Here, we address these problems using a commercially available silver-based gas diffusion electrode (used in industrial-scale chlorine–alkaline electrolysis) as the cathode in the CO2 electrolyser. Electric current densities up to 300 mA cm–2 were demonstrated for more than 1,200 hours with continuous operation. This CO2 electrolyser was coupled to a fermentation module, where the out-coming syngas from the CO2 electrolyser was converted to butanol and hexanol with high carbon selectivity. Conversion of photovoltaic electricity, CO2 and H2O to the desired alcohols achieved close to 100% Faradaic efficiency. Industrial production of useful and high-value chemicals via artificial photosynthesis is closer than expected with the proposed scalable hybrid system. The generation of useful chemicals from CO2 and renewable energy is an attractive—but challenging—endeavour. This work reports on the long-term operation of commercial electrodes for efficient CO2 reduction, with subsequent fermentation of the syngas product completing the technical photosynthesis of alcohols.
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