Coupling Electrochemical CO <sub>2</sub> Reduction With Ethanol Oxidation for Acetate Production in a Dual‐Electrolyzer System

A Anirudha Shekhawat (Analytical Chemistry – Center For Electrochemical Sciences (CES); Faculty of Chemistry and Biochemistry Ruhr University Bochum, Universitätsstr. 150 Bochum Germany) S Shubhadeep Chandra (Analytical Chemistry‐Center for Electrochemical Sciences (CES) Faculty of Chemistry and Biochemistry Ruhr University Bochum Bochum Germany) R Ridha Zerdoumi (Analytical Chemistry‐Center for Electrochemical Sciences (CES) Faculty of Chemistry and Biochemistry Ruhr University Bochum Bochum Germany) B Bashir Eid (Analytical Chemistry‐Center for Electrochemical Sciences (CES) Faculty of Chemistry and Biochemistry Ruhr University Bochum Bochum Germany) M Muhammad Adib Abdillah Mahbub (Analytical Chemistry‐Center for Electrochemical Sciences (CES) Faculty of Chemistry and Biochemistry Ruhr University Bochum Bochum Germany) W Wolfgang Schuhmann (Analytical Chemistry – Center For Electrochemical Sciences (CES); Faculty of Chemistry and Biochemistry Ruhr University Bochum, Universitätsstr. 150 Bochum Germany)

Abstract

ABSTRACT Bioethanol production from biomass is suggested as a strategy for greener fuel production. However, an equimolar amount of CO 2 is released during fermentation, making the process less efficient. Utilizing this released CO 2 directly in an electrolyzer can further reduce carbon emissions, ultimately reaching a CO 2 ‐negative carbon balance. We coupled the electrochemical CO 2 reduction reaction with ethanol oxidation as the anode reaction for acetate production. A nickel foam‐supported cobalt selenium catalyst, which is highly active for ethanol oxidation, reached a Faradaic efficiency of nearly 96% towards acetate. A high production rate of 95.2 µmol cm −2 min −1 at a current density of 1 A cm −2 in a model flow‐through electrolyzer was achieved. For coupled electrolysis at 100 mA cm −2 , we achieved 99% and 95% FE for CO and acetate at the cathode and anode, respectively. Furthermore, using a defect‐Cu‐triazole catalyst on the gas diffusion cathode, we show a tandem cell system coupled with ethanol oxidation in both reactors for selective acetate production. This proof‐of‐concept approach can be further developed for a greener approach to bioethanol and acetate production.

Article Details

Volume / Issue Vol. 65, Issue 20
Published May 11, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (6)

A

Anirudha Shekhawat

Analytical Chemistry – Center For Electrochemical Sciences (CES); Faculty of Chemistry and Biochemistry Ruhr University Bochum, Universitätsstr. 150 Bochum Germany

S

Shubhadeep Chandra

Analytical Chemistry‐Center for Electrochemical Sciences (CES) Faculty of Chemistry and Biochemistry Ruhr University Bochum Bochum Germany

R

Ridha Zerdoumi

Analytical Chemistry‐Center for Electrochemical Sciences (CES) Faculty of Chemistry and Biochemistry Ruhr University Bochum Bochum Germany

B

Bashir Eid

Analytical Chemistry‐Center for Electrochemical Sciences (CES) Faculty of Chemistry and Biochemistry Ruhr University Bochum Bochum Germany

M

Muhammad Adib Abdillah Mahbub

Analytical Chemistry‐Center for Electrochemical Sciences (CES) Faculty of Chemistry and Biochemistry Ruhr University Bochum Bochum Germany

W

Wolfgang Schuhmann

Analytical Chemistry – Center For Electrochemical Sciences (CES); Faculty of Chemistry and Biochemistry Ruhr University Bochum, Universitätsstr. 150 Bochum Germany