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      Cu-based catalyst designs in CO 2 electroreduction: precise modulation of reaction intermediates for high-value chemical generation

      review-article
      b , c , c , d , a , , b ,
      Chemical Science
      The Royal Society of Chemistry

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          Abstract

          The massive emission of excess greenhouse gases (mainly CO 2) have an irreversible impact on the Earth's ecology. Electrocatalytic CO 2 reduction (ECR), a technique that utilizes renewable energy sources to create highly reduced chemicals ( e.g. C 2H 4, C 2H 5OH), has attracted significant attention in the science community. Cu-based catalysts have emerged as promising candidates for ECR, particularly in producing multi-carbon products that hold substantial value in modern industries. The formation of multi-carbon products involves a range of transient intermediates, the behaviour of which critically influences the reaction pathway and product distribution. Consequently, achieving desirable products necessitates precise regulation of these intermediates. This review explores state-of-the-art designs of Cu-based catalysts, classified into three categories based on the different prospects of the intermediates' modulation: heteroatom doping, morphological structure engineering, and local catalytic environment engineering. These catalyst designs enable efficient multi-carbon generation in ECR by effectively modulating reaction intermediates.

          Abstract

          Product distribution during electrocatalytic CO 2 reduction is closely related to the behaviour of reaction intermediates. Morphological and microenvironmental engineering of Cu-based catalysts can regulate the reaction tendency of intermediates, enabling target products to be selectively obtained.

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          Progress and Perspectives of Electrochemical CO2 Reduction on Copper in Aqueous Electrolyte

          To date, copper is the only heterogeneous catalyst that has shown a propensity to produce valuable hydrocarbons and alcohols, such as ethylene and ethanol, from electrochemical CO2 reduction (CO2R). There are variety of factors that impact CO2R activity and selectivity, including the catalyst surface structure, morphology, composition, the choice of electrolyte ions and pH, and the electrochemical cell design. Many of these factors are often intertwined, which can complicate catalyst discovery and design efforts. Here we take a broad and historical view of these different aspects and their complex interplay in CO2R catalysis on Cu, with the purpose of providing new insights, critical evaluations, and guidance to the field with regard to research directions and best practices. First, we describe the various experimental probes and complementary theoretical methods that have been used to discern the mechanisms by which products are formed, and next we present our current understanding of the complex reaction networks for CO2R on Cu. We then analyze two key methods that have been used in attempts to alter the activity and selectivity of Cu: nanostructuring and the formation of bimetallic electrodes. Finally, we offer some perspectives on the future outlook for electrochemical CO2R.
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            CO2electroreduction to ethylene via hydroxide-mediated copper catalysis at an abrupt interface

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              How copper catalyzes the electroreduction of carbon dioxide into hydrocarbon fuels

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                Author and article information

                Journal
                Chem Sci
                Chem Sci
                SC
                CSHCBM
                Chemical Science
                The Royal Society of Chemistry
                2041-6520
                2041-6539
                16 October 2023
                6 December 2023
                16 October 2023
                : 14
                : 47
                : 13629-13660
                Affiliations
                [a ] State Key Laboratory for Organic Electronics and Information Displays & Institute of Advanced Materials IAM, Nanjing University of Posts & Telecommunications Nanjing 210023 China iamyangzhou@ 123456njupt.edu.cn
                [b ] State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University Nanjing 210023 China jjzhu@ 123456nju.edu.cn
                [c ] State Key Laboratory of Pollution Control and Resource Reuse, The Frontiers Science Center for Critical Earth Material Cycling, School of the Environment, Nanjing University Nanjing 210023 China
                [d ] Department of Nanoengineering, University of California La Jolla San Diego CA 92093 USA
                Author information
                https://orcid.org/0000-0001-6110-993X
                https://orcid.org/0000-0003-3795-306X
                https://orcid.org/0000-0002-8201-1285
                Article
                d3sc04353c
                10.1039/d3sc04353c
                10699555
                38075661
                c14e408d-5de2-4529-bee7-be2bd3456b8a
                This journal is © The Royal Society of Chemistry
                History
                : 20 August 2023
                : 13 October 2023
                Page count
                Pages: 32
                Funding
                Funded by: Natural Science Foundation of Jiangsu Province, doi 10.13039/501100004608;
                Award ID: BK20220405
                Award ID: BK20210189
                Funded by: National Natural Science Foundation of China, doi 10.13039/501100001809;
                Award ID: 22276100
                Award ID: 22176086
                Funded by: Nanjing University of Posts and Telecommunications, doi 10.13039/501100005374;
                Award ID: NY221006
                Categories
                Chemistry
                Custom metadata
                Paginated Article

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