4.8 Editorial Material

Electrochemical conversion of CO2 to long-chain hydrocarbons

Journal

JOULE
Volume 6, Issue 9, Pages 1978-1980

Publisher

CELL PRESS
DOI: 10.1016/j.joule.2022.08.012

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Funding

  1. U.S. Department of Energy's Office of Energy Efficiency and Renewable Energy (EERE) under the Advanced Manufacturing Office (AMO) [DE-EE0009418]

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The study presents a family of nickel oxygenate-derived electrocatalysts capable of converting CO2 into linear and branched C-3 to C-6 hydrocarbons with a combined Faradaic efficiency of up to 6.5%. Mechanistic investigations using advanced characterization tools and computational modeling identify the polarized Ni delta+ associated with Ni-O bonds as the active sites promoting carbon-carbon bond coupling.
Reporting recently in Nature Catalysis, Zhou et al. disclosed a family of nickel oxygenate-derived electrocatalysts that can convert CO2 to linear and branched C-3 to C-6 hydrocarbons with the combined Faradaic efficiencies of up to 6.5%. The study also revealed the polarized Ni delta+ associated with Ni-O bonds as the active sites in pro-moting carbon-carbon bond coupling through mechanistic investi-gations using advanced characterization tools and computational modeling

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