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Long-term stable and selective conversion of carbon dioxide to formate using dental amalgam electrode
•A newly developed dental amalgam electrode system enabled selective CO2-to-formate conversion for more than a month.•It showed a faradaic efficiency of 80–100 % for the formate production at a wide potential range of -1.5 to -2.3 V vs. Ag/AgCl.•The selectivity of the carbon conversion was 100 % in...
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Published in: | Journal of CO2 utilization 2021-03, Vol.45, p.101435, Article 101435 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | •A newly developed dental amalgam electrode system enabled selective CO2-to-formate conversion for more than a month.•It showed a faradaic efficiency of 80–100 % for the formate production at a wide potential range of -1.5 to -2.3 V vs. Ag/AgCl.•The selectivity of the carbon conversion was 100 % in the range of -1.6 to -2.3 V vs. Ag/AgCl.•The high concentration formate production up to 2.4 M (18 wt%) was obtained.
The process of electrochemical conversion of CO2 to a valuable chemical requires the use of an electrode material with high selectivity and stability. In this study, we successfully fabricated a dental amalgam composition on a copper foam electrode and demonstrated the selective conversion of CO2 to formate. The faradaic efficiency was 80–100 % at current densities ranging from 50 to 250 mA∙cm−2. The residual electricity was used solely to produce H2, and all the carbon atoms in CO2 were converted to formate. It enabled the easy separation of the highly water-soluble formate from the gaseous hydrogen. The produced formate concentration was up to 2.4 M (18 wt%), and the electrolyzer based on the dental amalgam electrode was effectively operated both continuously and intermittently for over a month. The results demonstrated the feasibility of the economic and large-scale CO2-to-formate conversion process. |
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ISSN: | 2212-9820 2212-9839 |
DOI: | 10.1016/j.jcou.2021.101435 |