Dantanarayana Ashwini, Housseini Wassim El, Beaver Kevin, Brachi Monica, McFadden Timothy P, Minteer Shelley D
Department of Chemistry, University of Utah, Salt Lake City, Utah 84112, United States.
Kummer Institute Center for Resource Sustainability, Missouri University of Science and Technology, Rolla, Missouri 65409, United States.
ACS Appl Bio Mater. 2024 Dec 16;7(12):8434-8443. doi: 10.1021/acsabm.4c01276. Epub 2024 Nov 20.
Microbial electrosynthesis (MES) is a rapidly growing technology at the forefront of sustainable chemistry, leveraging the ability of microorganisms to catalyze electrochemical reactions to synthesize valuable compounds from renewable energy sources. The reduction of CO is a major target application for MES, but research in this area has been stifled, especially with the use of direct electron transfer (DET)-based microbial systems. The major fundamental hurdle that needs to be overcome is the low efficiency of CO reduction largely attributed to minimal microbial access to CO owing to its low solubility in the electrolyte. With their tunable physical properties, ionic liquids present a potential solution to this challenge and have previously shown promise in facilitating efficient CO electroreduction by increasing the CO solubility. However, the use of ionic liquids in MES remains unexplored. In this study, we investigated the role of 1-ethyl-3-methylimidazolium acetate ([EMIM][Ac]) using MR-1 as a model DET strain. Electrochemical investigations demonstrated the ability of MR-1 biocathodes to directly convert CO to formate with a faradaic efficiency of 34.5 ± 26.1%. The addition of [EMIM][Ac] to the system significantly increased cathodic current density and enhanced the faradaic efficiency to 94.5 ± 4.3% while concurrently amplifying the product yield from 34 ± 23 μM to 366 ± 34 μM. These findings demonstrate that ionic liquids can serve as efficient, biocompatible cosolvents for microbial electrochemical reduction of CO to value-added products, holding promise for more robust applications of MES.
微生物电合成(MES)是可持续化学前沿领域中一项迅速发展的技术,它利用微生物催化电化学反应的能力,从可再生能源中合成有价值的化合物。CO的还原是MES的一个主要目标应用,但该领域的研究受到了阻碍,特别是在使用基于直接电子转移(DET)的微生物系统时。需要克服的主要基本障碍是CO还原效率低,这主要归因于CO在电解质中的溶解度低,微生物对其的接触极少。离子液体具有可调节的物理性质,为这一挑战提供了潜在的解决方案,并且此前已显示出通过提高CO溶解度来促进高效CO电还原的前景。然而,离子液体在MES中的应用仍未得到探索。在本研究中,我们以MR-1作为模型DET菌株,研究了1-乙基-3-甲基咪唑醋酸盐([EMIM][Ac])的作用。电化学研究表明,MR-1生物阴极能够将CO直接转化为甲酸盐,法拉第效率为34.5±26.1%。向系统中添加[EMIM][Ac]显著提高了阴极电流密度,并将法拉第效率提高到94.5±4.3%,同时将产物产率从34±23μM提高到366±34μM。这些发现表明,离子液体可以作为高效、生物相容的助溶剂,用于微生物将CO电化学还原为增值产物,为MES更强大的应用带来了希望。