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      Bubble Formation in the Electrolyte Triggers Voltage Instability in CO 2 Electrolyzers

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          Summary

          The electrochemical reduction of CO 2 is promising for mitigating anthropogenic greenhouse gas emissions; however, voltage instabilities currently inhibit reaching high current densities that are prerequisite for commercialization. Here, for the first time, we elucidate that product gaseous bubble accumulation on the electrode/electrolyte interface is the direct cause of the voltage instability in CO 2 electrolyzers. Although bubble formation in water electrolyzers has been extensively studied, we identified that voltage instability caused by bubble formation is unique to CO 2 electrolyzers. The appearance of syngas bubbles within the electrolyte at the gas diffusion electrode (GDE)-electrolyte chamber interface (i.e. ∼10% bubble coverage of the GDE surface) was accompanied by voltage oscillations of 60 mV. The presence of syngas in the electrolyte chamber physically inhibited two-phase reaction interfaces, thereby resulting in unstable cell performance. The strategic incorporation of our insights on bubble growth behavior and voltage instability is vital for designing commercially relevant CO 2 electrolyzers.

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          Highlights

          • X-ray imaging was used to characterize the bubble formation in a CO 2 electrolyzer

          • Gas formed near the GDE-electrolyte chamber interface and caused voltage instabilities

          • We hypothesize that gas physically inhibits two-phase reaction interfaces

          Abstract

          Electrochemical Energy Production; Mechanical Engineering Interfacial Electrochemistry

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          Most cited references26

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          CO2electroreduction to ethylene via hydroxide-mediated copper catalysis at an abrupt interface

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            CO2 electrolysis to multicarbon products at activities greater than 1 A cm−2

            Electrolysis offers an attractive route to upgrade greenhouse gases such as carbon dioxide (CO 2 ) to valuable fuels and feedstocks; however, productivity is often limited by gas diffusion through a liquid electrolyte to the surface of the catalyst. Here, we present a catalyst:ionomer bulk heterojunction (CIBH) architecture that decouples gas, ion, and electron transport. The CIBH comprises a metal and a superfine ionomer layer with hydrophobic and hydrophilic functionalities that extend gas and ion transport from tens of nanometers to the micrometer scale. By applying this design strategy, we achieved CO 2 electroreduction on copper in 7 M potassium hydroxide electrolyte (pH ≈ 15) with an ethylene partial current density of 1.3 amperes per square centimeter at 45% cathodic energy efficiency.
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              What Should We Make with CO 2 and How Can We Make It?

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                Author and article information

                Contributors
                Journal
                iScience
                iScience
                iScience
                Elsevier
                2589-0042
                23 April 2020
                22 May 2020
                23 April 2020
                : 23
                : 5
                : 101094
                Affiliations
                [1 ]Thermofluids for Energy and Advanced Materials Laboratory, Department of Mechanical and Industrial Engineering, Institute for Sustainable Energy, Faculty of Applied Science and Engineering, University of Toronto, 5 King's College Road, Toronto, ON M5S 3G8, Canada
                [2 ]Department of Civil Engineering, McMaster University, Hamilton, ON, L8S 4L7, Canada
                Author notes
                []Corresponding author abazylak@ 123456mie.utoronto.ca
                [3]

                Lead Contact

                Article
                S2589-0042(20)30279-0 101094
                10.1016/j.isci.2020.101094
                7214942
                32388400
                552732ee-a949-4960-8991-8a176e8b4d7a
                © 2020 The Author(s)

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 14 March 2020
                : 13 April 2020
                : 17 April 2020
                Categories
                Article

                electrochemical energy production,mechanical engineering interfacial electrochemistry

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