Selective and Energy Efficient Electrocatalytic CO <sub>2</sub> ‐to‐Ethanol Conversion through Anion Modulation

Y Yumin Da (Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore 117543, Singapore) J Jie Chen L Lei Fan R Rui Jiang (Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore, 117543, Singapore) Y Yukun Xiao (Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore 117543, Singapore) M Meng Wang G Ganwen Chen (Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore, 117543, Singapore) Z Zhangliu Tian H Hanqian Zhang (Agency for Science, Technology and Research (A*STAR) Advanced Remanufacturing and Technology Centre (ARTC) 3 CleanTech Loop, CleanTech Two Singapore 637143 Singapore) H Hongqiang Jin (Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore, 117543, Singapore) X Xiang Chen C Chenrui Ji (Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore, 117543, Singapore) S Shibo Xi Y Yanwei Lum (Department of Chemical and Biomolecular Engineering) L Lei Wang T Tong Zhu J Jia Zhang W Wei Chen

Abstract

Abstract Ethanol, with its high market value and stable global demand, stands out as an attractive product of electrocatalytic CO 2 reduction. However, achieving high ethanol selectivity and energy efficiency at industrial current densities remains challenging. In this study, we employed a blended anion modulation strategy to enhance the selectivity and energy efficiency of CO 2 ‐to‐ethanol conversion. The Cu 2 (OH) 3 F pre‐catalyst achieved Faradaic efficiencies of 50% and 93% for ethanol and C 2+ , respectively, at 700 mA cm −2 in a blended electrolyte consisting of 2 M KOH and 1 M KCl. Comprehensive electrochemical tests, combined with in situ characterizations and theoretical analysis, revealed that chloride and hydroxide increased *CO coverage for efficient C─C coupling. Moreover, hydroxide stabilizes the *CHCOH intermediate through hydrogen bonding with the adsorbed hydroxide on the catalyst surface, while Cl synergistically enhances its reactivity by promoting water dissociation toward the ethanol pathway.

Article Details

Volume / Issue Vol. 64, Issue 35
Published August 25, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (18)

Y

Yumin Da

Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore 117543, Singapore

J

Jie Chen

L

Lei Fan

R

Rui Jiang

Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore, 117543, Singapore

Y

Yukun Xiao

Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore 117543, Singapore

M

Meng Wang

G

Ganwen Chen

Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore, 117543, Singapore

Z

Zhangliu Tian

H

Hanqian Zhang

Agency for Science, Technology and Research (A*STAR) Advanced Remanufacturing and Technology Centre (ARTC) 3 CleanTech Loop, CleanTech Two Singapore 637143 Singapore

H

Hongqiang Jin

Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore, 117543, Singapore

X

Xiang Chen

C

Chenrui Ji

Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore, 117543, Singapore

S

Shibo Xi

Y

Yanwei Lum

Department of Chemical and Biomolecular Engineering

L

Lei Wang

T

Tong Zhu

J

Jia Zhang

W

Wei Chen