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      Sensitivity Analysis of One-Dimensional Multiphysics Simulation of CO 2 Electrolysis Cell

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          Abstract

          Electrochemical (EC) carbon dioxide (CO 2) reduction, where CO 2 is converted to value-added products such as fuel precursors, plays a key role in helping the world’s energy system reach net-zero carbon emissions. Simulations of EC cells provide valuable insight into their operation since detailed experimental results on short length and time scales are difficult to obtain. In this work, we construct a 1D simulation of a membrane-electrode-assembly EC cell for CO 2 reduction, using a porous silver gas diffusion cathode. We run the simulation under different electrolyte conditions, showing how the cell performance is affected. We then perform a sensitivity analysis of all input parameters to the simulation, which has not been presented before in the literature. We show that the CO partial current density ( i CO) is significantly affected by each input parameter of the simulation. i CO is most sensitive to EC kinetic parameters ( i 0/α) of all EC reactions, with a 1% change in α resulting in up to 6% change in i CO. Since there is uncertainty associated with the value of each input parameter, this indicates that infidelity between experiment and simulation is likely, and thus, caution should be practiced when comparing experimental results to simulation results. Further, we show that the large range of conditions simulated in literature helps to explain the large variance in reported values of i 0 and α. The results of this paper demonstrate the potential of sensitivity analysis methods to quickly optimize aspects of cell performance (CO 2 utilization, Faradaic efficiency, etc.).

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          Most cited references41

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          Net-zero emissions energy systems

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            Compilation of Henry's law constants (version 4.0) for water as solvent

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              Hydrolysis of Electrolyte Cations Enhances the Electrochemical Reduction of CO2 over Ag and Cu

              Electrolyte cation size is known to influence the electrochemical reduction of CO2 over metals; however, a satisfactory explanation for this phenomenon has not been developed. We report here that these effects can be attributed to a previously unrecognized consequence of cation hydrolysis occurring in the vicinity of the cathode. With increasing cation size, the pKa for cation hydrolysis decreases and is sufficiently low for hydrated K+, Rb+, and Cs+ to serve as buffering agents. Buffering lowers the pH near the cathode, leading to an increase in the local concentration of dissolved CO2. The consequences of these changes are an increase in cathode activity, a decrease in Faradaic efficiencies for H2 and CH4, and an increase in Faradaic efficiencies for CO, C2H4, and C2H5OH, in full agreement with experimental observations for CO2 reduction over Ag and Cu.
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                Author and article information

                Journal
                J Phys Chem C Nanomater Interfaces
                J Phys Chem C Nanomater Interfaces
                jy
                jpccck
                The Journal of Physical Chemistry. C, Nanomaterials and Interfaces
                American Chemical Society
                1932-7447
                1932-7455
                27 June 2024
                11 July 2024
                : 128
                : 27
                : 11131-11144
                Affiliations
                []School of Physics, Trinity College Dublin , Dublin D02 PN40, Ireland
                []MacDiarmid Institute for Advanced Materials and Nanotechnology and School of Chemical and Physical Sciences, Victoria University of Wellington , Wellington 6012, New Zealand
                Author notes
                Author information
                https://orcid.org/0000-0001-5033-631X
                https://orcid.org/0000-0002-0686-6898
                Article
                10.1021/acs.jpcc.4c00690
                11247494
                39015418
                b1e7badd-e073-471f-9637-f1c78a8ccc0e
                © 2024 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 31 January 2024
                : 23 May 2024
                : 17 May 2024
                Funding
                Funded by: Sustainable Energy Authority of Ireland, doi 10.13039/501100001603;
                Award ID: 211947 17084
                Categories
                Article
                Custom metadata
                jp4c00690
                jp4c00690

                Thin films & surfaces
                Thin films & surfaces

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