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Electrolysis of CO2 and H2O

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Electrolysis of CO2 and H2O ( electrolysis-co2-and-h2o )

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high-performance electrode materials. The experimental studies make extensive use of electrochemical impedance spectroscopy and systematic variation of test conditions to examine the electrochemical phenomena. Variation of the material composition itself within families of related materials was an additional parameter used in the electrode level and materials studies that revealed more information than studying a single material would have. Using full cells, the performance and durability of a solid oxide cell applied for co- electrolysis of CO2 and H2O was investigated. High initial performance was observed but the long-term durability needs to be improved. Based on these results, an analysis of the energy balance and economics of an electrolysis-based synthetic fuel production process, including CO2 air capture and Fischer-Tropsch fuel synthesis, determined that the system can feasibly operate at 70% electricity-to-liquid fuel efficiency (higher heating value basis) and that the price of electricity needed to produce competitive synthetic gasoline (at USD$2/gal, or $0.53/L, wholesale) is 2-3 U.S. cents per kWh. For $3/gal ($0.78/L) gasoline, 4-5 cents per kWh is needed. Fuel production may already be economical in some regions that have inexpensive renewable electricity, such as Iceland. The dominant costs of the process are the electricity cost and the capital cost of the electrolyzer, and this capital cost is significantly increased when operating intermittently (on renewable power sources such as solar and wind). Low cell internal resistance, low degradation, and low manufacturing cost each contribute to a low electrolyzer capital cost, and can be traded off. One straightforward path to affordability is by improving the durability of the high current density cell operation (≥1 A/cm2) that is already possible with these cells. The negative-electrode, a composite of nickel and yttria-stabilized zirconia (YSZ), is often the major site of cell degradation, including in the co-electrolysis results presented here. To better understand the reaction mechanisms at the negative-electrode that limit performance and durability, different metal electrodes including nickel were studied using a simplified point-contact electrode geometry with a well-defined three-phase boundary (TPB; the electrode/electrolyte/gas interface where the electrochemical reactions take place). The simple geometry is useful for isolating the electrochemical properties without the effects of the complex microstructure of technological porous electrodes. Widely different impedance responses of the different metals to the same changes in test conditions (gas composition, temperature, and polarization) were observed, indicating that the same reaction mechanisms are not shared by the different metals, contrary to some recent studies. Evidence was also found that supports the explanation that impurities segregated to the TPB play a major role and are largely responsible for inconsistencies in the electrode kinetics literature. The significance of microstructure at the TPB was also revealed – the electrode polarization resistance was reduced by an order of magnitude when subjected to extreme conditions of oxidation-reduction and strong cathodic polarization, which induced the formation of a micro/nanostructured TPB. Possible reaction mechanisms for H2O/CO2 reduction and H2/CO oxidation are discussed.

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