Harnessing Electrocatalytic Coupling of Carbon Dioxide and Methanol for High‐Efficiency Formic Acid Production

Z Zhikeng Zheng (School of Environmental Science and Engineering Sun Yat‐sen University Guangzhou 510275 China) X Xiaobo Zheng (Engineering Research Center of Advanced Rare Earth Materials, Department of Chemistry) L Ligang Wang (Institute of Molecular Plus, National Industry-Education Platform for Energy Storage) H Huiming Wen K Ke Li Z Zhenhao Xu (School of Environmental Science and Engineering Sun Yat‐sen University Guangzhou 510275 China) Y Yameng Fan (School of Science) P Peng Li S Suyu Zhang (School of Environmental Science and Engineering Sun Yat‐sen University Guangzhou 510275 China) B Bin Liu D Dingsheng Wang (Department of Chemistry) K Kai Yan G Guoxiu Wang (Center for Clean Energy Technology, School of Mathematical and Physical Sciences, Faculty of Science)

Abstract

AbstractThe coupling of electrocatalytic CO2 reduction (ECR) and methanol oxidation reaction (MOR) presents a promising strategy for simultaneous cogeneration of formic acid (FA) at both cathode and anode. However, sluggish kinetics, low selectivity and efficiency hinder practical application. Herein, we demonstrate an integrated ECR||MOR system employing CuBi cathode and NiCo anode for energy‐efficient FA cogeneration. The CuBi alloy achieves high Faradaic efficiencies (FE > 90%) for FA generation over an extensive potential range (>400 mV), attributed to the accelerated formation of HCOO* intermediates in facilitating FA production. Meanwhile, the NiCo alloy reached a remarkable FE of 97.5% for FA generation at 1.4 V versus reversible hydrogen electrode, benefiting from rapid HCOO* intermediate formation that effectively mitigates CO toxicity. This unique system delivered a current density of 10 mA cm−2 at a voltage of 2.07 V, representing a substantial reduction of 320 mV compared to water electrolysis. Across a wide operational voltage window (2.0–2.8 V), the system consistently delivered total Faradaic efficiencies ranging between 189% and 192%, alongside exceptional FA production capacities surpassing 400 g kWh−1, which significantly outperformed traditional methods (∼220 g kWh−1). This work provides an efficient pathway for low‐energy CO2 utilization and sustainable FA production.

Article Details

Volume / Issue Vol. 64, Issue 43
Published October 20, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (13)

Z

Zhikeng Zheng

School of Environmental Science and Engineering Sun Yat‐sen University Guangzhou 510275 China

X

Xiaobo Zheng

Engineering Research Center of Advanced Rare Earth Materials, Department of Chemistry

L

Ligang Wang

Institute of Molecular Plus, National Industry-Education Platform for Energy Storage

H

Huiming Wen

K

Ke Li

Z

Zhenhao Xu

School of Environmental Science and Engineering Sun Yat‐sen University Guangzhou 510275 China

Y

Yameng Fan

School of Science

P

Peng Li

S

Suyu Zhang

School of Environmental Science and Engineering Sun Yat‐sen University Guangzhou 510275 China

B

Bin Liu

D

Dingsheng Wang

Department of Chemistry

K

Kai Yan

G

Guoxiu Wang

Center for Clean Energy Technology, School of Mathematical and Physical Sciences, Faculty of Science