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CO2 conversion to synthetic fuels using flow cell reactor over Cu and Ag based cathodes

As a result of electrochemical conversion of carbon dioxide (CO 2 ), value-added chemicals like as synthetic fuels and chemical feedstocks can be produced. In the current state of the art, copper-based materials are most widely used being the most effective catalysts for this reaction. It is still n...

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Published in:Materials for renewable and sustainable energy 2024-08, Vol.13 (2), p.233-241
Main Authors: Zignani, Sabrina C., Aricò, Antonino S.
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description As a result of electrochemical conversion of carbon dioxide (CO 2 ), value-added chemicals like as synthetic fuels and chemical feedstocks can be produced. In the current state of the art, copper-based materials are most widely used being the most effective catalysts for this reaction. It is still necessary to improve the reaction rate and product selectivity of CuOx for electrochemical CO 2 reduction reaction (CO 2 RR). The main objective of this work was synthesized and evaluate the copper oxide electrocatalyst combined with silver (CuO 70% Ag 30%) for the conversion of carbon dioxide into synthetic fuels. The catalysts have been prepared by the oxalate method and assessed in a flow cell system. The results of electrochemical experiments were carried out at room temperature and at different potentials (-1.05 V–0.75 V vs. RHE in presence of 0.1 M KHCO 3 ) and gas and liquid chromatographic analysis are summarized. The CuOx-based electrodes demonstrated the selective of ~ 25% at -0.55 V for formic acid (HCOOH) and over CuO -Ag and selective of ethylene at ~ 20% over CuOx at -1.05 V. Other products were formed as ethylene, ethanol, and propanol (C 2 H 4 , EtOH, PrOH) at more positive potentials. On the other hand, carbon monoxide, acetate, ethylene glycol, propinaldehyde, glycoaldehyde and glyoxal (CO, CH 3 COO, C 2 H 6 O 2 , C 3 H 6 O, C 2 H 4 O 2 , C 2 H 2 O 2 ) have been formed and detected. Based on the results of these studies, it appears that the formation of synthetic fuels from CO 2 at room temperature in alkaline environment can be very promising.
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Other products were formed as ethylene, ethanol, and propanol (C 2 H 4 , EtOH, PrOH) at more positive potentials. On the other hand, carbon monoxide, acetate, ethylene glycol, propinaldehyde, glycoaldehyde and glyoxal (CO, CH 3 COO, C 2 H 6 O 2 , C 3 H 6 O, C 2 H 4 O 2 , C 2 H 2 O 2 ) have been formed and detected. 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In the current state of the art, copper-based materials are most widely used being the most effective catalysts for this reaction. It is still necessary to improve the reaction rate and product selectivity of CuOx for electrochemical CO 2 reduction reaction (CO 2 RR). The main objective of this work was synthesized and evaluate the copper oxide electrocatalyst combined with silver (CuO 70% Ag 30%) for the conversion of carbon dioxide into synthetic fuels. The catalysts have been prepared by the oxalate method and assessed in a flow cell system. The results of electrochemical experiments were carried out at room temperature and at different potentials (-1.05 V–0.75 V vs. RHE in presence of 0.1 M KHCO 3 ) and gas and liquid chromatographic analysis are summarized. The CuOx-based electrodes demonstrated the selective of ~ 25% at -0.55 V for formic acid (HCOOH) and over CuO -Ag and selective of ethylene at ~ 20% over CuOx at -1.05 V. 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subjects Acetic acid
Carbon dioxide
Carbon monoxide
Catalysts
Cathodes
Chemical reduction
Chemical synthesis
Chemistry and Materials Science
Chromatography
CO2 conversion
Copper
Copper converters
Copper oxide
Copper oxides
Electrocatalysts
Electrochemistry
Ethanol
Ethylene glycol
Flow electrochemical cell
Formic acid
Fuels
Materials Science
No critical raw catalyst
Original Paper
Propanol
Renewable and Green Energy
Room temperature
Silver
Synthetic fuels
title CO2 conversion to synthetic fuels using flow cell reactor over Cu and Ag based cathodes
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