TY - JOUR
T1 - Ethylene Electrosynthesis via Selective CO2 Reduction
T2 - Fundamental Considerations, Strategies, and Challenges
AU - O' Carroll, Thomas
AU - Yang, Xiaoxuan
AU - Gordon, Kenneth J.
AU - Fei, Ling
AU - Wu, Gang
N1 - Publisher Copyright:
© 2024 Wiley-VCH GmbH.
PY - 2024/9/6
Y1 - 2024/9/6
N2 - The electrochemical carbon dioxide reduction reaction (CO2RR) is a promising approach for reducing atmospheric carbon dioxide (CO2) emissions, allowing harmful CO2 to be converted into more valuable carbon-based products. On one hand, single carbon (C1) products have been obtained with high efficiency and show great promise for industrial CO2 capture. However, multi-carbon (C2+) products possess high market value and have demonstrated significant promise as potential products for CO2RR. Due to CO2RR's multiple pathways with similar equilibrium potentials, the extended reaction mechanisms necessary to form C2+ products continue to reduce the overall selectivity of CO2-to-C2+ electroconversion. Meanwhile, CO2RR as a whole faces many challenges relating to system optimization, owing to an intolerance for low surface pH, systemic stability and utilization issues, and a competing side reaction in the form of the H2 evolution reaction (HER). Ethylene (C2H4) remains incredibly valuable within the chemical industry; however, the current established method for producing ethylene (steam cracking) contributes to the emission of CO2 into the atmosphere. Thus, strategies to significantly increase the efficiency of this technology are essential. This review will discuss the vital factors influencing CO2RR in forming C2H4 products and summarize the recent advancements in ethylene electrosynthesis.
AB - The electrochemical carbon dioxide reduction reaction (CO2RR) is a promising approach for reducing atmospheric carbon dioxide (CO2) emissions, allowing harmful CO2 to be converted into more valuable carbon-based products. On one hand, single carbon (C1) products have been obtained with high efficiency and show great promise for industrial CO2 capture. However, multi-carbon (C2+) products possess high market value and have demonstrated significant promise as potential products for CO2RR. Due to CO2RR's multiple pathways with similar equilibrium potentials, the extended reaction mechanisms necessary to form C2+ products continue to reduce the overall selectivity of CO2-to-C2+ electroconversion. Meanwhile, CO2RR as a whole faces many challenges relating to system optimization, owing to an intolerance for low surface pH, systemic stability and utilization issues, and a competing side reaction in the form of the H2 evolution reaction (HER). Ethylene (C2H4) remains incredibly valuable within the chemical industry; however, the current established method for producing ethylene (steam cracking) contributes to the emission of CO2 into the atmosphere. Thus, strategies to significantly increase the efficiency of this technology are essential. This review will discuss the vital factors influencing CO2RR in forming C2H4 products and summarize the recent advancements in ethylene electrosynthesis.
KW - CO electroreduction
KW - Cu electrocatalysts
KW - electrocatalysis
KW - ethylene electrosynthesis
UR - http://www.scopus.com/inward/record.url?scp=85195500653&partnerID=8YFLogxK
U2 - 10.1002/aenm.202401558
DO - 10.1002/aenm.202401558
M3 - Review article
AN - SCOPUS:85195500653
SN - 1614-6832
VL - 14
JO - Advanced Energy Materials
JF - Advanced Energy Materials
IS - 33
M1 - 2401558
ER -