TY - JOUR
T1 - Nitrogen-Rich Porous-Conjugated Framework for Efficient Capture and Electroreduction of Simulated Flue Gas in Acidic Electrolyte
AU - Liu, Weiyi
AU - Lv, Zunhang
AU - Li, Xin
AU - Wang, Changli
AU - Tian, Chongao
AU - Feng, Xiao
AU - Wang, Bo
AU - Yang, Wenxiu
N1 - Publisher Copyright:
© 2025 American Chemical Society.
PY - 2025/7/9
Y1 - 2025/7/9
N2 - Achieving the integration of simulated flue gas catalysis with acidic eCO2RR represents a highly promising and economically viable strategy for industrialization, yet remains unexplored. Here, with the design of a nitrogen-rich conjugated framework (CAU-35), we first report the successful demonstration of highly efficient conversion of simulated flue gas to formic acid in an acidic environment, while further unveiling a novel mechanism of protonation-enhanced adsorption. Through the integrated construction of capture and catalysis, the system can achieve an unprecedented Faradaic efficiency of 96.6% for formic acid production and a remarkable single-pass conversion efficiency up to 71.4% in a flow cell, surpassing the performance of conventional alkaline systems and those utilizing pure CO2 as a feedstock. Moreover, comparative studies with the nitrogen-free analogue (CAU-7) unequivocally demonstrate that the anomalous enhancement in acidic acid stems from material protonation. Further complemented by molecular dynamics simulations, the novel mechanism is uncovered by which material protonation can enhance CO2 adsorption and catalytic performance via optimization of interfacial interaction. These fundamental insights provide critical principles for system optimization and microenvironmental design, paving the way for the practical implementation of eCO2RR technologies.
AB - Achieving the integration of simulated flue gas catalysis with acidic eCO2RR represents a highly promising and economically viable strategy for industrialization, yet remains unexplored. Here, with the design of a nitrogen-rich conjugated framework (CAU-35), we first report the successful demonstration of highly efficient conversion of simulated flue gas to formic acid in an acidic environment, while further unveiling a novel mechanism of protonation-enhanced adsorption. Through the integrated construction of capture and catalysis, the system can achieve an unprecedented Faradaic efficiency of 96.6% for formic acid production and a remarkable single-pass conversion efficiency up to 71.4% in a flow cell, surpassing the performance of conventional alkaline systems and those utilizing pure CO2 as a feedstock. Moreover, comparative studies with the nitrogen-free analogue (CAU-7) unequivocally demonstrate that the anomalous enhancement in acidic acid stems from material protonation. Further complemented by molecular dynamics simulations, the novel mechanism is uncovered by which material protonation can enhance CO2 adsorption and catalytic performance via optimization of interfacial interaction. These fundamental insights provide critical principles for system optimization and microenvironmental design, paving the way for the practical implementation of eCO2RR technologies.
UR - http://www.scopus.com/pages/publications/105009439588
U2 - 10.1021/jacs.5c07519
DO - 10.1021/jacs.5c07519
M3 - Article
AN - SCOPUS:105009439588
SN - 0002-7863
VL - 147
SP - 24023
EP - 24031
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 27
ER -