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CO2 Reduction Selective for C?2 Products on Polycrystalline Copper with N-Substituted Pyridinium Additives.


ABSTRACT: Electrocatalytic CO2 reduction to generate multicarbon products is of interest for applications in artificial photosynthetic schemes. This is a particularly attractive goal for CO2 reduction by copper electrodes, where a broad range of hydrocarbon products can be generated but where selectivity for C-C coupled products relative to CH4 and H2 remains an impediment. Herein we report a simple yet highly selective catalytic system for CO2 reduction to C?2 hydrocarbons on a polycrystalline Cu electrode in bicarbonate aqueous solution that uses N-substituted pyridinium additives. Selectivities of 70-80% for C2 and C3 products with a hydrocarbon ratio of C?2/CH4 significantly greater than 100 have been observed with several additives. 13C-labeling studies verify CO2 to be the sole carbon source in the C?2 hydrocarbons produced. Upon electroreduction, the N-substituted pyridinium additives lead to film deposition on the Cu electrode, identified in one case as the reductive coupling product of N-arylpyridinium. Product selectivity can also be tuned from C?2 species to H2 (?90%) while suppressing methane with certain N-heterocyclic additives.

SUBMITTER: Han Z 

PROVIDER: S-EPMC5571460 | biostudies-literature | 2017 Aug

REPOSITORIES: biostudies-literature

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CO<sub>2</sub> Reduction Selective for C<sub>≥2</sub> Products on Polycrystalline Copper with N-Substituted Pyridinium Additives.

Han Zhiji Z   Kortlever Ruud R   Chen Hsiang-Yun HY   Peters Jonas C JC   Agapie Theodor T  

ACS central science 20170721 8


Electrocatalytic CO<sub>2</sub> reduction to generate multicarbon products is of interest for applications in artificial photosynthetic schemes. This is a particularly attractive goal for CO<sub>2</sub> reduction by copper electrodes, where a broad range of hydrocarbon products can be generated but where selectivity for C-C coupled products relative to CH<sub>4</sub> and H<sub>2</sub> remains an impediment. Herein we report a simple yet highly selective catalytic system for CO<sub>2</sub> reduct  ...[more]

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