Ionomer‐Driven Reaction Microenvironment Control in Bicarbonate‐Mediated Integrated CO <sub>2</sub> Capture and Electrolysis

Y Youwen Rong (Department of Chemistry Advanced Institute for Future Energy Shanghai Key Laboratory of Electrochemical and Thermochemical Conversion for Resources Recycling State Key Laboratory of Porous Materials for Separation and Conversion iChEM (Collaborative Innovation Center of Chemistry for Energy Materials) Fudan University Shanghai 200433 China) C Chuanchuan Yan (State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 China) X Xiaotong Li (Department of Chemistry and Organic and Carbon Electronics Laboratories (ORaCEL)) J Jing Liu X Xiaozhi Su (Shanghai Synchrotron Radiation Facility, Zhangjiang Laboratory, Shanghai Advanced Research Institute) G Guohui Zhang (State Key Laboratory of Catalysis) D Dunfeng Gao (State Key Laboratory of Catalysis Dalian Institute of Chemical Physics) G Guoxiong Wang (State Key Laboratory of Catalysis, Dalian National Laboratory for Clean Energy, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials) Dalian Institute of Chemical Physics) X Xinhe Bao (State Key Laboratory of Catalysis, Dalian National Laboratory for Clean Energy, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials) Dalian Institute of Chemical Physics)

Abstract

Abstract Bicarbonate electrolysis coupling upstream CO 2 capture with electrochemical conversion of captured CO 2 presents an energy‐efficient alternative to existing CO 2 electrolysis route. Yet, its practical application is impeded by unsatisfactory reaction rate and energy efficiency. Here, we have improved the bicarbonate electrolysis performance through manipulating reaction microenvironments by introducing ionomers into cobalt phthalocyanine (CoPc) electrodes. The Nafion‐incorporated CoPc electrode exhibits a maximum CO partial current density of 410 mA cm −2 at a low cell voltage of 3.09 V in a cation exchange membrane‐based zero‐gap electrolyzer. Electrode structure characterization and finite element simulation results indicate that the proton conductivity of the Nafion ionomer increases the local concentration of in situ generated CO 2 around CoPc catalyst, resulting in impressive CO production performance. A closed‐loop demonstration using the Nafion‐incorporated CoPc electrode and a simulated flue gas underscores the great promise of the bicarbonate‐mediated integrated CO 2 capture and electrolysis process.

Article Details

Volume / Issue Vol. 65, Issue 7
Published February 09, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (9)

Y

Youwen Rong

Department of Chemistry Advanced Institute for Future Energy Shanghai Key Laboratory of Electrochemical and Thermochemical Conversion for Resources Recycling State Key Laboratory of Porous Materials for Separation and Conversion iChEM (Collaborative Innovation Center of Chemistry for Energy Materials) Fudan University Shanghai 200433 China

C

Chuanchuan Yan

State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 China

X

Xiaotong Li

Department of Chemistry and Organic and Carbon Electronics Laboratories (ORaCEL)

J

Jing Liu

X

Xiaozhi Su

Shanghai Synchrotron Radiation Facility, Zhangjiang Laboratory, Shanghai Advanced Research Institute

G

Guohui Zhang

State Key Laboratory of Catalysis

D

Dunfeng Gao

State Key Laboratory of Catalysis Dalian Institute of Chemical Physics

G

Guoxiong Wang

State Key Laboratory of Catalysis, Dalian National Laboratory for Clean Energy, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials) Dalian Institute of Chemical Physics

X

Xinhe Bao

State Key Laboratory of Catalysis, Dalian National Laboratory for Clean Energy, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials) Dalian Institute of Chemical Physics