4.6 Article

Electrolytic conversion of carbon capture solutions containing carbonic anhydrase

Journal

JOURNAL OF INORGANIC BIOCHEMISTRY
Volume 231, Issue -, Pages -

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jinorgbio.2022.111782

Keywords

Heterogeneous catalysis; Carbonic anhydrase; Carbon dioxide; Electroreduction; Carbon capture; Bicarbonate

Funding

  1. Natural Sciences and Engineering Research Council of Canada [CRDPJ 536621 - 18]
  2. TotalEnergies American Services, Inc. (an affiliate of TotalEnergies SE, France)
  3. Max Planck-UBC-UTokyo Center for Quantum Materials
  4. Canada First Research Excellence Fund, Quantum Materials and Future Technologies Program
  5. Canadian Foundation for Innovation [229288]
  6. Canadian Institute for Advanced Research [BSE-BERL-162173]
  7. UBC Four Year Doctoral Fellowship program
  8. NSERC

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The electrolysis of carbon capture solutions can convert them into carbon-based products without the need for energy-intensive CO2 recovery steps. Carbonic anhydrase enzymes can enhance CO2 capture by increasing the reaction rate between CO2 and alkaline solutions. A carbon microporous layer can suppress the deactivation of the catalyst caused by carbonic anhydrase.
The electrolysis of carbon capture solutions bypasses energy-intensive CO2 recovery steps that are often required to convert CO2 into value-added products. We report herein an electrochemical flow reactor that converts carbon capture solutions containing carbonic anhydrase enzymes into carbon-based products. Carbonic anhydrase enzymes benefit CO2 capture by increasing the rate of reaction between CO2 and weakly alkaline solutions by 20 fold. In this study, we reduced CO2-enriched bicarbonate solutions containing carbonic anhydrase ( enzymatic CO2 capture solutions ) into CO at current densities of 100 mA cm(-2). This result demonstrated how to electrolyse enzymatic CO2 capture solutions, but the selectivity for CO production was two-thirds less than bicarbonate solutions without carbonic anhydrase. This reduction in performance occurred because carbonic anhydrase deactivated the catalyst surface. A carbon microporous layer was found to suppress this deactivation.

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