Direct Electron Transfer-Type Gas Diffusion Electrodefor Efficient CO2-to-Formate Bioconversion acrossBroad and Low CO2 Levels

Abstract Bioelectrocatalytic CO2 reduction to value-added chemicals offers a sustainable route for carbon recycling; however, achieving high activity under low CO2 conditions remains a major challenge. Herein, we report a direct electron transfer (DET)-type gas diffusion electrode (GDE) utilizing formate dehydrogenase 1 (FoDH1) from Methylorubrum extorquens AM1 for efficient CO2-to-formate conversion across a broad range of low CO2 levels. The electrode surface was modified with pyrene derivatives using multiwalled carbon nanotubes (MWCNTs) to tailor the enzyme–electrode interface, enabling favorable enzyme orientation for rapid electron transfer. A 1-pyrenemethylamine (PyNH2)-modified GDE with FoDH1 exhibited a current density of −1.2 mA cm–2 at a reduction potential of −0.9 V, which was twice that of the pristine electrode, and generated formate with a Faradaic efficiency of 82 ± 5%, outperforming previously reported GDE systems. Kinetic analyses under controlled CO2 conditions (0.04–100%) revealed a notably low apparent Michaelis constant (KM,app) of 2.6 ± 0.3%, which is less than one-third of that of the solution system, indicating high CO2 affinity. This enhancement is attributed to the direct supply of gaseous CO2 to the catalytic layer, avoiding equilibrium limitations in the electrolyte solution. These results lead to a promising tool for enzymatic CO2 reduction using emission gases from industrial sources and provide key design principles for practical CO2-recycling technologies.