TY - JOUR
T1 - Electron effect regulation
T2 - A study on the influence of electron-donating and withdrawing group modification on the performance of metal-coordinated catalysts for electrochemical carbon dioxide reduction
AU - Yu, Jiaqi
AU - Zhang, Hongsen
AU - Liu, Qi
AU - Yu, Jing
AU - Song, Dalei
AU - Xiong, Chu an
AU - Li, Ying
AU - Li, Rumin
AU - Wang, Jun
N1 - Publisher Copyright:
© 2024 Elsevier Inc.
PY - 2025/4
Y1 - 2025/4
N2 - Electron effect regulation is a crucial factor influencing the activity and selectivity of Cu-based coordination compound catalysts in the electrochemical carbon dioxide reduction reaction (CO2RR). Despite significant progress, the structure–activity relationship and the underlying regulatory mechanisms warrant further in-depth investigation. In this study, three types of Cu-[O[sbnd]N[sbnd]N[sbnd]O] tetradentate coordination molecular catalysts with varying electron densities, namely Cu-N2O2, methoxy-modified Cu-N2O2 (Cu-EDG-N2O2), and nitro-modified Cu-N2O2 (Cu-EWG-N2O2), were prepared using a substituent regulation strategy. The prepared catalyst's micromorphology and structural characteristics were analyzed using various characterization methods. Systematic electrocatalytic CO2RR experiments were conducted to evaluate the performance of these catalysts. Compared to the unmodified Cu-N2O2, the Cu-EDG-N2O2 catalyst exhibited superior reduction performance for CH4 and C2H4 products. At an applied potential of −1.7 V vs. the reversible hydrogen electrode, the Faradaic efficiencies for CH4 and C2H4 of Cu-EDG-N2O2 were 37.8 ± 2.2 % and 25.0 ± 0.5 %, respectively. In contrast, the Cu-EWG-N2O2 catalyst demonstrated higher activity towards the production of H2 as a by-product. The effects of electronic properties of substitutions on catalyst performance were revealed by combining experimental characterization and theoretical simulation. The results showed that the conjugation effect of the –OCH3 group facilitates faster electron transfer between Cu and CO2, thereby enhancing CO2RR activity. Additionally, the introduction of different substituents modulates the local microenvironment around the Cu active centers, significantly influencing the catalytic performance. This study provides valuable theoretical and experimental insights into the design of efficient Cu-N2O2-type metal coordination electrocatalysts for CO2RR processes.
AB - Electron effect regulation is a crucial factor influencing the activity and selectivity of Cu-based coordination compound catalysts in the electrochemical carbon dioxide reduction reaction (CO2RR). Despite significant progress, the structure–activity relationship and the underlying regulatory mechanisms warrant further in-depth investigation. In this study, three types of Cu-[O[sbnd]N[sbnd]N[sbnd]O] tetradentate coordination molecular catalysts with varying electron densities, namely Cu-N2O2, methoxy-modified Cu-N2O2 (Cu-EDG-N2O2), and nitro-modified Cu-N2O2 (Cu-EWG-N2O2), were prepared using a substituent regulation strategy. The prepared catalyst's micromorphology and structural characteristics were analyzed using various characterization methods. Systematic electrocatalytic CO2RR experiments were conducted to evaluate the performance of these catalysts. Compared to the unmodified Cu-N2O2, the Cu-EDG-N2O2 catalyst exhibited superior reduction performance for CH4 and C2H4 products. At an applied potential of −1.7 V vs. the reversible hydrogen electrode, the Faradaic efficiencies for CH4 and C2H4 of Cu-EDG-N2O2 were 37.8 ± 2.2 % and 25.0 ± 0.5 %, respectively. In contrast, the Cu-EWG-N2O2 catalyst demonstrated higher activity towards the production of H2 as a by-product. The effects of electronic properties of substitutions on catalyst performance were revealed by combining experimental characterization and theoretical simulation. The results showed that the conjugation effect of the –OCH3 group facilitates faster electron transfer between Cu and CO2, thereby enhancing CO2RR activity. Additionally, the introduction of different substituents modulates the local microenvironment around the Cu active centers, significantly influencing the catalytic performance. This study provides valuable theoretical and experimental insights into the design of efficient Cu-N2O2-type metal coordination electrocatalysts for CO2RR processes.
KW - CO reduction
KW - Coordination environment
KW - Cu-based coordination catalyst
KW - Electron effect regulation
KW - Substituent effect
UR - https://www.scopus.com/pages/publications/85212121869
U2 - 10.1016/j.jcis.2024.12.085
DO - 10.1016/j.jcis.2024.12.085
M3 - Article
C2 - 39693877
AN - SCOPUS:85212121869
SN - 0021-9797
VL - 683
SP - 387
EP - 397
JO - Journal of Colloid and Interface Science
JF - Journal of Colloid and Interface Science
ER -