TY - JOUR
T1 - Acidic CO2 electroreduction for high CO2 utilization
T2 - catalysts, electrodes, and electrolyzers
AU - Lee, Taemin
AU - Lee, Yujin
AU - Eo, Jungsu
AU - Nam, Dae Hyun
N1 - Publisher Copyright:
© 2024 The Royal Society of Chemistry.
PY - 2023/12/19
Y1 - 2023/12/19
N2 - The electrochemical carbon dioxide (CO2) reduction reaction (CO2RR) is considered a promising technology for converting atmospheric CO2 into value-added compounds by utilizing renewable energy. The CO2RR has developed in various ways over the past few decades, including product selectivity, current density, and catalytic stability. However, its commercialization is still unsuitable in terms of economic feasibility. One of the major challenges in its commercialization is the low single-pass conversion efficiency (SPCE) of CO2, which is primarily caused by the formation of carbonate (CO32−) in neutral and alkaline electrolytes. Notably, the majority of CO2RRs take place in such media, necessitating significant energy input for CO2 regeneration. Therefore, performing the CO2RR under conditions that minimize CO32− formation to suppress reactant and electrolyte ion loss is regarded an optimal strategy for practical applications. Here, we introduce the recent progress and perspectives in the electrochemical CO2RR in acidic electrolytes, which receives great attention because of the inhibition of CO32− formation. This includes the categories of nanoscale catalytic design, microscale microenvironmental effects, and bulk scale applications in electrolyzers for zero carbon loss reactions. Additionally, we offer insights into the issue of limited catalytic durability, a notable drawback under acidic conditions and propose guidelines for further development of the acidic CO2RR.
AB - The electrochemical carbon dioxide (CO2) reduction reaction (CO2RR) is considered a promising technology for converting atmospheric CO2 into value-added compounds by utilizing renewable energy. The CO2RR has developed in various ways over the past few decades, including product selectivity, current density, and catalytic stability. However, its commercialization is still unsuitable in terms of economic feasibility. One of the major challenges in its commercialization is the low single-pass conversion efficiency (SPCE) of CO2, which is primarily caused by the formation of carbonate (CO32−) in neutral and alkaline electrolytes. Notably, the majority of CO2RRs take place in such media, necessitating significant energy input for CO2 regeneration. Therefore, performing the CO2RR under conditions that minimize CO32− formation to suppress reactant and electrolyte ion loss is regarded an optimal strategy for practical applications. Here, we introduce the recent progress and perspectives in the electrochemical CO2RR in acidic electrolytes, which receives great attention because of the inhibition of CO32− formation. This includes the categories of nanoscale catalytic design, microscale microenvironmental effects, and bulk scale applications in electrolyzers for zero carbon loss reactions. Additionally, we offer insights into the issue of limited catalytic durability, a notable drawback under acidic conditions and propose guidelines for further development of the acidic CO2RR.
UR - http://www.scopus.com/inward/record.url?scp=85182371100&partnerID=8YFLogxK
U2 - 10.1039/d3nr05480b
DO - 10.1039/d3nr05480b
M3 - Review article
C2 - 38193364
AN - SCOPUS:85182371100
SN - 2040-3364
VL - 16
SP - 2235
EP - 2249
JO - Nanoscale
JF - Nanoscale
IS - 5
ER -