TY - JOUR
T1 - In Situ Observation of Post-CO Intermediates to Decode C─C Coupling Pathways in CO2 Electroreduction
AU - Sun, Mingxu
AU - Rocabado, David S.Rivera
AU - Cheng, Jiamin
AU - Noguchi, Tomohiro G.
AU - Donoshita, Masaki
AU - Matsuu, Takahiro
AU - Higashi, Manabu
AU - Fujigaya, Tsuyohiko
AU - Ishimoto, Takayoshi
AU - Yamauchi, Miho
N1 - Publisher Copyright:
© 2025 The Author(s). Angewandte Chemie International Edition published by Wiley-VCH GmbH.
PY - 2025/7/21
Y1 - 2025/7/21
N2 - Electrocatalytic carbon dioxide (CO2) reduction reaction (CO2RR) has emerged as a promising strategy for sustainable energy conversion and carbon utilization. Despite intensive research efforts, the understanding of intermediates and pathways leading from CO2RR to multicarbon (C2+) chemicals remains incomplete. The challenge is to gain insight into the activation of adsorbed CO and the subsequent pathways. Here, we design a specially tailored Cu nanowire array facing a hydrophobic interface as an electrode to highly enhance Raman signals in the in situ environment, allowing sensitive observation of the sequential change of various elusive intermediates during CO2RR, such as CO, CH2, CO coexisting with CH2, CH2CO, and CH3. Density functional theory calculations reveal that the C─C coupling during CO2RR originates from an asymmetric coupling between CH2 and CO to form CH2CO, identified as the rate-determining step in the formation of C2+ products. These findings deepen the understanding of the C─C coupling processes, which are crucial for advancing catalyst development in electrochemical CO2 upgrading.
AB - Electrocatalytic carbon dioxide (CO2) reduction reaction (CO2RR) has emerged as a promising strategy for sustainable energy conversion and carbon utilization. Despite intensive research efforts, the understanding of intermediates and pathways leading from CO2RR to multicarbon (C2+) chemicals remains incomplete. The challenge is to gain insight into the activation of adsorbed CO and the subsequent pathways. Here, we design a specially tailored Cu nanowire array facing a hydrophobic interface as an electrode to highly enhance Raman signals in the in situ environment, allowing sensitive observation of the sequential change of various elusive intermediates during CO2RR, such as CO, CH2, CO coexisting with CH2, CH2CO, and CH3. Density functional theory calculations reveal that the C─C coupling during CO2RR originates from an asymmetric coupling between CH2 and CO to form CH2CO, identified as the rate-determining step in the formation of C2+ products. These findings deepen the understanding of the C─C coupling processes, which are crucial for advancing catalyst development in electrochemical CO2 upgrading.
KW - Carbon dioxide reduction reaction
KW - C─C coupling pathways
KW - Density functional theory calculations
KW - Post-CO intermediates
KW - Raman spectroscopy
UR - https://www.scopus.com/pages/publications/105006631438
UR - https://www.scopus.com/pages/publications/105006631438#tab=citedBy
U2 - 10.1002/anie.202502740
DO - 10.1002/anie.202502740
M3 - Article
C2 - 40338611
AN - SCOPUS:105006631438
SN - 1433-7851
VL - 64
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 30
M1 - e202502740
ER -