TY  - JOUR
T1  - A carbon-based single-atom Cu electrocatalyst for efficient conversion of CO2 to carbon products
AU  - Huang, Bo
AU  - Zhao, Fang
AU  - Fu, Jiantao
AU  - Zheng, Lirong
AU  - Zhang, Jiatao
AU  - Zhao, Di
N1  - Publisher Copyright:
© 2025 The Royal Society of Chemistry.
PY  - 2025/10/7
Y1  - 2025/10/7
N2  - The simultaneous and efficient electroreduction of CO2 to C1 and C2 different phase products is an extremely challenging task due to the competitive reaction of hydrogen evolution, high energy barrier of CO2 activation and C-C coupling. Herein, an N-doped carbon-based single-atom Cu-based electrocatalyst (Cu-N4/C) was designed, which can efficiently reduce CO2 to carbon products with a total Faraday efficiency (CO and ethanol) of 94.67%. Among them, the selectivity of ethanol reached 53.11%. And Cu-N4/C could also maintain excellent stability within 16 h. In situ infrared spectroscopy showed that the intermediates, such as *COB, *OCH2, *CO-*OCH2, and OC2H5, which appeared during the electrocatalytic reaction of Cu-N4/C, promoted the generation of both CO and ethanol, leading to an extremely high carbon product efficiency. This work elucidates the active center of the Cu-N4/C electrocatalyst as well as the reason for the highly selective generation of carbon products, and provides a new perspective for subsequent in-depth exploration of the rational design of CO2RR electrocatalysts.
AB  - The simultaneous and efficient electroreduction of CO2 to C1 and C2 different phase products is an extremely challenging task due to the competitive reaction of hydrogen evolution, high energy barrier of CO2 activation and C-C coupling. Herein, an N-doped carbon-based single-atom Cu-based electrocatalyst (Cu-N4/C) was designed, which can efficiently reduce CO2 to carbon products with a total Faraday efficiency (CO and ethanol) of 94.67%. Among them, the selectivity of ethanol reached 53.11%. And Cu-N4/C could also maintain excellent stability within 16 h. In situ infrared spectroscopy showed that the intermediates, such as *COB, *OCH2, *CO-*OCH2, and OC2H5, which appeared during the electrocatalytic reaction of Cu-N4/C, promoted the generation of both CO and ethanol, leading to an extremely high carbon product efficiency. This work elucidates the active center of the Cu-N4/C electrocatalyst as well as the reason for the highly selective generation of carbon products, and provides a new perspective for subsequent in-depth exploration of the rational design of CO2RR electrocatalysts.
UR  - http://www.scopus.com/pages/publications/105017959845
U2  - 10.1039/d5cc04310g
DO  - 10.1039/d5cc04310g
M3  - Article
C2  - 40947986
AN  - SCOPUS:105017959845
SN  - 1359-7345
VL  - 61
SP  - 15822
EP  - 15825
JO  - Chemical Communications
JF  - Chemical Communications
IS  - 81
ER  -