Microbial electrosynthesis from CO2 reaches productivity of syngas and chain elongation fermentations
O. Cabau Peinado (TU Delft - BT/Bioprocess Engineering)
Marijn Winkelhorst (TU Delft - BT/Bioprocess Engineering)
R. Stroek (TU Delft - BT/Industriele Microbiologie)
Roderick de Kat Angelino (Student TU Delft)
A.J.J. Straathof (TU Delft - BT/Bioprocess Engineering)
Kunal Masania (TU Delft - Group Masania)
Jean Marc Daran (TU Delft - BT/Industriele Microbiologie)
Ludovic Jourdin (TU Delft - BT/Bioprocess Engineering)
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Abstract
Carbon-based products are essential to society, yet producing them from fossil fuels is unsustainable. Microorganisms have the ability to take up electrons from solid electrodes and convert carbon dioxide (CO2) to valuable carbon-based chemicals. However, higher productivities and energy efficiencies are needed to reach a viability that can make the technology transformative. Here, we show how a biofilm-based microbial porous cathode in a directed flow-through electrochemical system can continuously reduce CO2 to even-chain C2–C6 carboxylic acids over 248 days. We demonstrate a threefold higher biofilm concentration, volumetric current density, and productivity compared with the state of the art. Most notably, the volumetric productivity (VP) resembles those achieved in laboratory-scale and industrial syngas (CO-H2-CO2) fermentation and chain elongation fermentation. This work highlights key design parameters for efficient electricity-driven microbial CO2 reduction. There is need and room to improve the rates of electrode colonization and microbe-specific kinetics to scale up the technology.
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