Enzymatic Flow Electrolyzer for CO <sub>2</sub> and Waste Comproportionation to Formate and Its Use in Photocatalytic Alkene Hydrocarboxylation

B Beverly Q. L. Low (Yusuf Hamied Department of Chemistry University of Cambridge Lensfield Road Cambridge CB2 1EW UK) S Santiago Rodríguez‐Jiménez (Yusuf Hamied Department of Chemistry University of Cambridge Lensfield Road Cambridge CB2 1EW UK) A Andrea Rogolino (Yusuf Hamied Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, U.K.) S Samuel J. Cobb (Yusuf Hamied Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, U.K.) C Chen Han (Yusuf Hamied Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, U.K.) G Guilherme Martins (Instituto de Tecnologia Química e Biológica António Xavier (ITQB NOVA), Universidade NOVA de Lisboa, Av. da República, 2780-157 Oeiras, Portugal) I Inês A. C. Pereira (Instituto de Tecnologia Química e Biológica António Xavier (ITQB NOVA), Universidade NOVA de Lisboa, Av. da República, 2780-157 Oeiras, Portugal) E Erwin Reisner

Abstract

Abstract Paired electrolysis enables the simultaneous coupling of CO 2 reduction with anodic waste upcycling to form valuable products. However, achieving selective, efficient, and stable product formation and coupling to downstream valorization remains a challenge. In this study, W‐containing formate dehydrogenase from Nitratidesulfovibrio vulgaris Hildenborough is immobilized onto a cathode made from carbon felt coated with porous TiO 2 and paired with a commercial Ni foam anode to assemble a semiartificial flow electrolyzer for the simultaneous conversion of CO 2 and waste (plastic and biomass) to the single product formate. The enzymatic flow electrolyzer achieved an initial cell faradaic efficiency toward formate of almost 200%, a maximum CO 2 conversion yield of 18% and can operate at a low full‐cell voltage of −1.5 V for 122 h, which allows for bias‐free operation with a silicon photovoltaic cell. The aqueous formate produced in the enzymatic electrolyzer was subsequently utilized downstream as a C 1 building block in the photocatalytic hydrocarboxylation of alkenes, providing a path for the domino valorization of CO 2 and waste toward bulk and fine chemical synthesis.

Article Details

Volume / Issue Vol. 64, Issue 46
Published November 10, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (8)

B

Beverly Q. L. Low

Yusuf Hamied Department of Chemistry University of Cambridge Lensfield Road Cambridge CB2 1EW UK

S

Santiago Rodríguez‐Jiménez

Yusuf Hamied Department of Chemistry University of Cambridge Lensfield Road Cambridge CB2 1EW UK

A

Andrea Rogolino

Yusuf Hamied Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, U.K.

S

Samuel J. Cobb

Yusuf Hamied Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, U.K.

C

Chen Han

Yusuf Hamied Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, U.K.

G

Guilherme Martins

Instituto de Tecnologia Química e Biológica António Xavier (ITQB NOVA), Universidade NOVA de Lisboa, Av. da República, 2780-157 Oeiras, Portugal

I

Inês A. C. Pereira

Instituto de Tecnologia Química e Biológica António Xavier (ITQB NOVA), Universidade NOVA de Lisboa, Av. da República, 2780-157 Oeiras, Portugal

E

Erwin Reisner