Dec 4, 2024
9:45am - 10:00am
Hynes, Level 2, Room 205
Cathal Burns1,2,Elizabeth Gibson2,Shafeer Kalathil1
Northumbria University1,Newcastle University2
Cathal Burns1,2,Elizabeth Gibson2,Shafeer Kalathil1
Northumbria University1,Newcastle University2
Converting atmospheric carbon dioxide emissions and water into value-added liquid multi-carbon products (e.g medium-chain fatty acids (MCFA’s)) and O<sub>2</sub> remains a difficult undertaking. Here, we present a semi-biological photoelectrochemical (PEC) system consisting of a scalable and cheap CuBi<sub>2</sub>O<sub>4</sub> photocathode (stabilized by MgO), with <i>Sporomusa ovata</i> grown on the electrode surface, a known CO<sub>2</sub>-fixing acetogenic and electrotrophic bacteria<sup>1-3</sup>. The PEC biohybrid effectively produces acetate and ethanol (as well as H<sub>2</sub> and O<sub>2</sub>) after 140 hours of stable operation (>5.5 days), without the need for any sacrificial organic additives. The PEC system splits water into its core elements forming O<sub>2</sub> on the anode and providing H<sub>2</sub> and electrons via the photocathode to living <i>S. ovata</i> cells to utilize as reducing equivalents for synthesis of acetate and ethanol from waste carbon dioxide. Chain elongation was then performed on the photosynthesised acetate and ethanol via fermentation using Clostridium kluyveri which produced butyrate (C4) and caproate (C6). Spectroelectrochemistry (cyclic voltammetry and UV-Vis spectroscopy), transient absorption spectroscopy, and attenuated total reflection infrared spectroscopy were also used to probe the biointerface and gain a deeper mechanistic understanding of these biohybrid systems. This semi-artificial photosynthetic approach demonstrates the advantages of synergistically pairing biotechnology with materials science as a promising method to use waste carbon dioxide as a feedstock for solar chemical production.<br/><br/><b>References:</b><br/>Wang et al., 2022 Nat. Catal. 5 633-641<br/>Yang et al., Nano Lett. 2021, 21, 5453–5456<br/>Su et al., Joule 4, 800–811