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      How Temperature Affects the Selectivity of the Electrochemical CO 2 Reduction on Copper

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          Abstract

          Copper is a unique catalyst for the electrochemical CO 2 reduction reaction (CO2RR) as it can produce multi-carbon products, such as ethylene and propanol. As practical electrolyzers will likely operate at elevated temperatures, the effect of reaction temperature on the product distribution and activity of CO2RR on copper is important to elucidate. In this study, we have performed electrolysis experiments at different reaction temperatures and potentials. We show that there are two distinct temperature regimes. From 18 up to ∼48 °C, C2+ products are produced with higher Faradaic efficiency, while methane and formic acid selectivity decreases and hydrogen selectivity stays approximately constant. From 48 to 70 °C, it was found that HER dominates and the activity of CO2RR decreases. Moreover, the CO2RR products produced in this higher temperature range are mainly the C1 products, namely, CO and HCOOH. We argue that CO surface coverage, local pH, and kinetics play an important role in the lower-temperature regime, while the second regime appears most likely to be related to structural changes in the copper surface.

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          Most cited references64

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          Combining theory and experiment in electrocatalysis: Insights into materials design

          Electrocatalysis plays a central role in clean energy conversion, enabling a number of sustainable processes for future technologies. This review discusses design strategies for state-of-the-art heterogeneous electrocatalysts and associated materials for several different electrochemical transformations involving water, hydrogen, and oxygen, using theory as a means to rationalize catalyst performance. By examining the common principles that govern catalysis for different electrochemical reactions, we describe a systematic framework that clarifies trends in catalyzing these reactions, serving as a guide to new catalyst development while highlighting key gaps that need to be addressed. We conclude by extending this framework to emerging clean energy reactions such as hydrogen peroxide production, carbon dioxide reduction, and nitrogen reduction, where the development of improved catalysts could allow for the sustainable production of a broad range of fuels and chemicals.
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            What would it take for renewably powered electrosynthesis to displace petrochemical processes?

            Electrocatalytic transformation of carbon dioxide (CO 2 ) and water into chemical feedstocks offers the potential to reduce carbon emissions by shifting the chemical industry away from fossil fuel dependence. We provide a technoeconomic and carbon emission analysis of possible products, offering targets that would need to be met for economically compelling industrial implementation to be achieved. We also provide a comparison of the projected costs and CO 2 emissions across electrocatalytic, biocatalytic, and fossil fuel–derived production of chemical feedstocks. We find that for electrosynthesis to become competitive with fossil fuel–derived feedstocks, electrical-to-chemical conversion efficiencies need to reach at least 60%, and renewable electricity prices need to fall below 4 cents per kilowatt-hour. We discuss the possibility of combining electro- and biocatalytic processes, using sequential upgrading of CO 2 as a representative case. We describe the technical challenges and economic barriers to marketable electrosynthesized chemicals.
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              New insights into the electrochemical reduction of carbon dioxide on metallic copper surfaces

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                Author and article information

                Journal
                ACS Catal
                ACS Catal
                cs
                accacs
                ACS Catalysis
                American Chemical Society
                2155-5435
                01 June 2023
                16 June 2023
                : 13
                : 12
                : 8080-8091
                Affiliations
                []Leiden Institute of Chemistry, Leiden University , P.O.Box 9502, 2300 RA Leiden, The Netherlands
                []Inorganic Chemistry and Catalysis group, Debye Institute for Nanomaterials Science and Institute for Sustainable and Circular Chemistry, Utrecht University , Universiteitsweg 99, 3584 CG Utrecht, The Netherlands
                Author notes
                Author information
                https://orcid.org/0000-0003-1810-1179
                https://orcid.org/0000-0002-4863-8105
                https://orcid.org/0000-0001-8155-5400
                https://orcid.org/0000-0001-5245-1426
                https://orcid.org/0000-0001-6777-4594
                Article
                10.1021/acscatal.3c00706
                10278069
                37342834
                5cee3bb6-d9b4-4ddd-bc7a-f9b1b02f929c
                © 2023 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
                : 16 February 2023
                : 22 May 2023
                Funding
                Funded by: Ministerie van Economische Zaken, doi 10.13039/501100003195;
                Award ID: NA
                Funded by: Materials innovation institute, doi 10.13039/501100011741;
                Award ID: NA
                Funded by: Tata Steel, doi 10.13039/501100007220;
                Award ID: NA
                Funded by: Nederlandse Organisatie voor Wetenschappelijk Onderzoek, doi 10.13039/501100003246;
                Award ID: NA
                Categories
                Research Article
                Custom metadata
                cs3c00706
                cs3c00706

                co2 reduction,temperature,copper,selectivity,co coverage,raman spectroscopy,surface reconstruction

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