Domino electroreduction of CO2 to methanol on a molecular catalyst

Yueshen Wu; Zhan Jiang; Lu Xu; Yongye Liang; Hailiang Wang

doi:10.1038/s41586-019-1760-8

Keywords

CatalysisMethanolElectrocatalystPhthalocyanineChemistryFaraday efficiencySelectivityCobaltCarbon nanotubeElectrochemical reduction of carbon dioxideElectrochemistryInorganic chemistryPhotochemistryCombinatorial chemistryMaterials scienceElectrodeOrganic chemistryNanotechnologyCarbon monoxidePhysical chemistry

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Publication Info

Year: 2019
Type: article
Volume: 575
Issue: 7784
Pages: 639-642
Citations: 1086
Access: Closed

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APA Style

                            
                                
                                    Yueshen Wu, 
                                
                                    Zhan Jiang, 
                                
                                    Lu Xu
                                
                                et al.
                            
                            (2019). 
                            Domino electroreduction of CO2 to methanol on a molecular catalyst. 
                            Nature
                            , 575
                            (7784)
                            , 639-642.
                            https://doi.org/10.1038/s41586-019-1760-8
                        

Identifiers

DOI: 10.1038/s41586-019-1760-8

Domino electroreduction of CO2 to methanol on a molecular catalyst

Keywords

Affiliated Institutions

Related Publications

Homogeneously Catalyzed Electroreduction of Carbon Dioxide—Methods, Mechanisms, and Catalysts

Electrocatalytic hydrogen evolution by cobalt difluoroboryl-diglyoximate complexes

Design of Single-Atom Co–N<sub>5</sub> Catalytic Site: A Robust Electrocatalyst for CO<sub>2</sub> Reduction with Nearly 100% CO Selectivity and Remarkable Stability

Electrochemical Reduction of Oxygen on Carbon Supported Pt and Pt/Ru Fuel Cell Electrodes in Alkaline Solutions

CO <sub>2</sub> electroreduction to ethylene via hydroxide-mediated copper catalysis at an abrupt interface

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