Electrochemical reduction of carbon dioxide (CO RR) product distribution has been identified to be dependent on various surface factors, including the Cu facet, morphology, chemical states, doping, etc., which can alter the binding strength of key intermediates such as *CO and *OCCO during reduction. Therefore, in-depth knowledge of the Cu catalyst surface and identification of the active species under reaction conditions aid in designing efficient Cu-based electrocatalysts. This progress report categorizes various Cu-based electrocatalysts into four main groups, namely metallic Cu, Cu alloys, Cu compounds (Cu + non-metal), and supported Cu-based catalysts (Cu supported by carbon, metal oxides, or polymers). The detailed mechanisms for the selective CO RR are presented, followed by recent relevant developments on the synthetic procedures for preparing Cu and Cu-based nanoparticles. Herein, the potential link between the Cu surface and CO RR performance is highlighted, especially in terms of the chemical states, but other significant factors such as defective sites and roughened morphology of catalysts are equally considered during the discussion of current studies of CO RR with Cu-based electrocatalysts to fully understand the origin of the significant enhancement toward C formation. This report concludes by providing suggestions for future designs of highly selective and stable Cu-based electrocatalysts for CO RR.
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http://dx.doi.org/10.1002/adma.201908398 | DOI Listing |
ChemSusChem
December 2024
Huazhong University of Science and Technology, School of Chemistry and Chemical Engineering, Luoyu load, 430074, Wuhan, CHINA.
Electrochemical carbon dioxide reduction reaction (CO2RR) to highly value-added C2+ fuels or chemicals is a promising pathway to address environment issues and energy crisis. In the periodic table, Cu as only the candidate can convert CO2 to C2+ products such as C2H4 and C2H5OH due to the suitable absorption energy to reaction intermediate. Application of Cu is limited for its low activity and poor selectivity.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
Key Laboratory of Superlight Materials and Surface Technology, Ministry of Education, College of Materials Science and Chemical Engineering, Harbin Engineering University, Harbin 150001, China.
Electron effect regulation is a crucial factor influencing the activity and selectivity of Cu-based coordination compound catalysts in the electrochemical carbon dioxide reduction reaction (CORR). Despite significant progress, the structure-activity relationship and the underlying regulatory mechanisms warrant further in-depth investigation. In this study, three types of Cu-[ONNO] tetradentate coordination molecular catalysts with varying electron densities, namely Cu-NO, methoxy-modified Cu-NO (Cu-EDG-NO), and nitro-modified Cu-NO (Cu-EWG-NO), were prepared using a substituent regulation strategy.
View Article and Find Full Text PDFJ Mater Chem A Mater
December 2024
Laboratory of Inorganic Materials and Catalysis, Department of Chemical Engineering and Chemistry, Eindhoven University of Technology P.O. Box 513 5600 MB Eindhoven The Netherlands
The electroreduction of CO (CORR) is a promising alternative to the direct CO electroreduction reaction (CO2RR) to produce C products. Cu-based electrocatalysts enable the formation of C-C bonds, leading to various C hydrocarbon and oxygenate products. Herein, we investigated how the composition of bimetallic Cu-Ag catalysts impacted the nature of the Cu-Ag interactions and the product distribution of the CORR, aiming to improve the selectivity to C products.
View Article and Find Full Text PDFWater Res
December 2024
MIIT Key Laboratory of Critical Materials Technology for New Energy Conversion and Storage, School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin 150001, China. Electronic address:
Angew Chem Int Ed Engl
December 2024
Department of Chemistry, Zhejiang University, Hangzhou, 310058, China.
Electrosynthesis of ammonia (NH) from nitrate (NO ) using renewable energy holds promise as a supplementary alternative to the Haber-Bosch process for NH production. Most research focuses on tuning the catalytic activity of metal catalysts by modification of the catalyst structures. However, the electrode supports which could influence the catalytic activity have not been well-explored.
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