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- CO2 Reduktion (1)
- Clostridium ragsdalei (1)
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For the realization of a sustainable energy economy, it is of great importance to develop CO2 -neutral methods producing multi-carbon organic chemicals used as feedstock in the chemical industry as well as carbon-neutral fuels. A promising method to alleviate the greenhouse effect and thereby forming value-added chemicals or syngas as an energy carrier, is through the electrochemical CO2 reduction reaction (CO2RR). In this work, a bioelectrotechnological approach is developed, in which the CO2RR reaction products (CO and H2) are directly fed to bacteria (acetogens), who use them as “reduction equivalents” to further metabolize CO2 to valuable carbon compounds. Therefore, a bio-electrochemical system consisting of a bioreactor coupled to a CO2 electrolysis cell will be established. Currently, scarce catalysts such as Ag and Au are used as for the CO2RR which may hamper the use of decentral CO2 conversion technology for cost reasons.
The technological viability of the bacteria-assisted electrolysis depends on the usage of efficient, biocompatible, and selective electrocatalysts prepared from inexpensive precursors. Porous transition metal and nitrogen co-doped carbons (M-N-Cs) have emerged as precious-metal free electrocatalysts for the direct electrochemical reduction of CO2 into CO and are excellent candidates for scale-up and deployment in technological applications. Furthermore, Co/Ni/Zn functioning as the catalytically active sites will be used, as they are expected to depict non-bactericidal properties in contrast to Cu and Ag catalysts. The non-bactericidal property could e.g., allow for application within the hybrid device (bio-electrochemical system), without the need to separate bacteria and cathode catalyst. The MNCs with the most promising electrocatalytic activity and selectivity will be evaluated in abiotic conditions in the hybrid bio-electrochemical reactor system.
Lithium-ion batteries (LIBs) are one technology to overcome the challenges of climate and energy crisis. They are widely used in electric vehicles, consumer electronics, or as storage for renewable energy sources. However, despite innovations in batteries' components like cathode and anode materials, separators, and electrolytes, the aging mechanism related to metallic aluminum current collector degradation causes a significant drop in their performance and prevents the durable use of LIBs. Glow-discharge optical emission spectroscopy (GD-OES) is a powerful method for depth-profiling of batteries' electrode materials. This work investigates aging-induced aluminum deposition on commercial lithium cobalt oxide (LCO) batteries' cathodes. The results illustrate the depth-resolved elemental distribution from the cathode surface to the current collector. An accumulation of aluminum is found on the cathode surface by GD-OES, consistent with results from energy-dispersive X-ray spectroscopy (EDX) combined with focused ion beam (FIB) cutting. In comparison to FIB-EDX, GD-OES allows a fast and manageable depth-profiling. Results from different positions on an aged cathode indicate an inhomogeneous aluminum film growth on the surface. The conclusions from these experiments can lead to a better understanding of the degradation of the aluminum current collector, thus leading to higher lifetimes of LIBs.