Issue |
MATEC Web Conf.
Volume 386, 2023
2023 International Conference on Materials Engineering, New Energy and Chemistry (MENEC 2023)
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Article Number | 03011 | |
Number of page(s) | 6 | |
Section | Energy Science and Environmental Studies | |
DOI | https://doi.org/10.1051/matecconf/202338603011 | |
Published online | 01 November 2023 |
Upgrading CO2 Into Fuels And Chemicals Via Electrocatalysis
School of Design and Engineering, National University of Singapore, 138600 Singapore, Singapore
* Corresponding author: e0973792@u.nus.edu
Converting carbon dioxide (CO2) into useful chemicals through electrochemical reduction reactions (CO2R) has received growing interest because it can be used to reduce greenhouse gas emissions and generate valuable chemical products. This report discusses the CO2 electrochemical reduction for carbon recycling and the production of valuable chemicals and fuels. It provides an overview of CO2 reduction reaction and a diverse of different CO2 conversion pathway. This research focuses on the mechanisms and catalytic materials used in CO2 electrocatalysis, with a specific emphasis on copper as a unique catalyst. It also highlights the factors that influence CO2 reduction, such as pH, presence of ions, temperature, pressure, electrode fouling, and catalyst deactivation. Furthermore, the economic and environmental aspects of CO2 reduction are explored, including the potential market prices and the positive environmental impacts. The report concludes by addressing the challenges and difficulties faced in electrocatalytic CO2 reduction, such as high activation energy, competing reactions, catalyst poisoning, and low current density. Overall, electrochemical CO2 reduction holds significant potential for sustainable and eco-friendly chemical production.
© The Authors, published by EDP Sciences, 2023
This is an Open Access article distributed under the terms of the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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