Enhancing microbial CO2 electrocatalysis for multicarbon reduction in a wet amine‐based catholyte

Author:

Su Kim Hui12,Lee Sangmin13ORCID,Moon Myounghoon1,Jong Jung Hwi12,Lee Jiye1,Chu Young‐Hwan4,Rae Kim Jung5,Kim Danbee1,Woo Park Gwon1,Hyun Ko Chang2,Youn Lee Soo1

Affiliation:

1. Gwangju Clean Energy Research Center Korea Institute of Energy Research 61003 Gwangju South Korea

2. Department of Chemical Engineering Chonnam National University 61186 Gwangju South Korea

3. Bio-Environmental Chemistry Chungnam National University 34134 Daejeon South Korea

4. Energy AI ⋅ Computational Science Laboratory Korea Institute of Energy Research 34129 Daejeon South Korea

5. School of Chemical and Biomolecular Engineering Pusan National University 46241 Pusan South Korea

Abstract

AbstractMicrobial CO2 electroreduction (mCO2ER) offers a promising approach for producing high‐value multicarbon reductants from CO2 by combining CO2 fixing microorganisms with conducting materials (i. e., cathodes). However, the solubility and availability of CO2 in an aqueous electrolyte pose significant limitations in this system. This study demonstrates the efficient production of long‐chain multicarbon reductants, specifically carotenoids (~C40), within a wet amine‐based catholyte medium during mCO2ER. Optimizing the concentration of the biocompatible CO2 absorbent, monoethanolamine (MEA), led to enhanced CO2 fixation in the electroautotroph bacteria. Molecular biological analyses revealed that MEA in the catholyte medium redirected the carbon flux towards carotenoid biosynthesis during mCO2ER. The faradaic efficiency of mCO2ER with MEA for carotenoid production was 4.5‐fold higher than that of the control condition. These results suggest the mass transport bottleneck in bioelectrochemical systems could be effectively addressed by MEA‐assissted mCO2ER, enabling highly efficient production of valuable products from CO2.

Publisher

Wiley

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