Differential Adsorption on Synergistic Cu─Cd Sites Enables Direct Hydrogenation in Acidic CO <sub>2</sub> Electroreduction

L Liyuan Zhou L Lebin Cai (State Key Laboratory of New Textile Materials and Advanced Processing Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education) Hubei Key Laboratory of Material Chemistry and Service Failure School of Chemistry and Chemical Engineering Huazhong University of Science and Technology (HUST) Wuhan China) W Wensheng Fang (State Key Laboratory of New Textile Materials and Advanced Processing Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education) Hubei Key Laboratory of Material Chemistry and Service Failure School of Chemistry and Chemical Engineering Huazhong University of Science and Technology (HUST) Wuhan China) D Deyu Zhu (School of Basic Medical Sciences) R Ruijuan Qi (Key Laboratory of Polar Materials and Devices (MOE), Department of Electronics) F Fuqing Yu (State Key Laboratory of New Textile Materials and Advanced Processing, Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education), Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering) H Ho Seok Park (School of Chemical Engineering, Sungkyunkwan University (SKKU), 2066, Seobu-ro, Jangan-gu, Suwon, Gyeonggi-do 16419, Republic of Korea) F Fei Song (Shanghai Synchrotron Radiation Facility, Shanghai Advanced Research Institute) B Bao Yu Xia (State Key Laboratory of New Textile Materials and Advanced Processing, Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education), Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering)

Abstract

Abstract The direct involvement of proton in acidic CO 2 reduction is key to boosting energy efficiency and preventing carbonate formation. However, the competitive adsorption of proton at low overpotential limits CO production by inhibiting the activation and hydrogenation of CO 2 to form the key intermediates, * COOH. To address this challenge, we developed a Cu─Cd alloy catalyst, which optimizes the proton‐coupled electron transfer (PCET) pathway through a synergistic regulation between dual Cu and Cd active sites. In situ spectroscopy and theoretical calculations reveal that Cd incorporation enhances * CO 2 adsorption and lowers the energy barrier for * COOH formation. By proving direct electrochemical hydrogenation, our catalyst achieved a remarkable CO Faradaic efficiency (FE) of 98.6% at −1.12 V versus RHE, and operated for over 250 h at a total current of 0.4 A under a voltage of 2.55 V in a proton exchange membrane electrode assembly. This research presents a powerful new insight for high‐performance acidic CO 2 electrolysis in proton‐abundant electrolyte environments.

Article Details

Volume / Issue Vol. 65, Issue 6
Published February 02, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (9)

L

Liyuan Zhou

L

Lebin Cai

State Key Laboratory of New Textile Materials and Advanced Processing Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education) Hubei Key Laboratory of Material Chemistry and Service Failure School of Chemistry and Chemical Engineering Huazhong University of Science and Technology (HUST) Wuhan China

W

Wensheng Fang

State Key Laboratory of New Textile Materials and Advanced Processing Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education) Hubei Key Laboratory of Material Chemistry and Service Failure School of Chemistry and Chemical Engineering Huazhong University of Science and Technology (HUST) Wuhan China

D

Deyu Zhu

School of Basic Medical Sciences

R

Ruijuan Qi

Key Laboratory of Polar Materials and Devices (MOE), Department of Electronics

F

Fuqing Yu

State Key Laboratory of New Textile Materials and Advanced Processing, Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education), Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering

H

Ho Seok Park

School of Chemical Engineering, Sungkyunkwan University (SKKU), 2066, Seobu-ro, Jangan-gu, Suwon, Gyeonggi-do 16419, Republic of Korea

F

Fei Song

Shanghai Synchrotron Radiation Facility, Shanghai Advanced Research Institute

B

Bao Yu Xia

State Key Laboratory of New Textile Materials and Advanced Processing, Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education), Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering