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dc.contributor.authorREIS, E. A. dos
dc.contributor.authorSILVA, G. T. S. T. da
dc.contributor.authorSANTIAGO, E. I.
dc.contributor.authorRIBEIRO, C.
dc.date.accessioned2024-01-15T10:40:59Z-
dc.date.available2024-01-15T10:40:59Z-
dc.date.created2023-03-16
dc.date.issued2023
dc.identifier.citationEnergy Technology, 2201367, 2023.
dc.identifier.issn2194-4296
dc.identifier.urihttp://www.alice.cnptia.embrapa.br/alice/handle/doc/1152433-
dc.descriptionElectrochemical CO2 reduction to fuels or commodity chemicals using renewable energy has drawn attention as a strategy for closing the anthropogenic chemical carbon cycle. More than that, enhancing the C?C coupling between the intermediates could lead to producing a range of high-value multi-carbon molecules. Although the research mainly focuses on the aqueous media for the electrochemical CO2 reduction reaction (eRRCO2), using nonaqueous electrolytes has the advantage of suppressing the hydrogen evolution reaction, controlling the protonassisted reduction reactions, and favoring the C?C coupling. Herein, the use of nonaqueous electrolytes for eRRCO2 and the components of the electrochemical reactor that affect the selectivity of the reaction are revisited. This review provides a perspective view of recent findings compared to well-established papers while presenting what is known about eRRCO2 in nonaqueous media.
dc.language.isoeng
dc.rightsopenAccess
dc.subjectElectrochemical CO2 reduction
dc.subjectMulti-carbon molecules
dc.titleRevisiting Electrocatalytic CO2 Reduction in Nonaqueous Media: Promoting CO2 Recycling in Organic Molecules by Controlling H2 Evolution.
dc.typeArtigo de periódico
dc.format.extent218 p.
riaa.ainfo.id1152433
riaa.ainfo.lastupdate2024-01-12
dc.identifier.doi10.1002/ente.202201367
dc.contributor.institutionEDUARDO ARIZONO DOS REIS, UNIVERSIDADE DE SÃO PAULO
dc.contributor.institutionELISABETE I. SANTIAGO, UNIVERSIDADE FEDERAL DE SÃO CARLOSeng
dc.contributor.institutionCAUE RIBEIRO DE OLIVEIRA, CNPDIA.eng
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