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CO <sub>2</sub> electrolysis to multicarbon products at activities greater than 1 A cm <sup>−2</sup>

2020· article· en· 1,458 citations· W3005205992 on OpenAlex· 10.1126/science.aay4217

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Canadian affiliationAn author listed a Canadian institution. This is the only route the usual frame has.
Canadian funderA Canadian agency funded it. The work may carry no Canadian affiliation at all.

Machine scores (provisional)

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

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Opus teacher head0.015
GPT teacher head0.238
Teacher spread
0.223 · how far apart the two teachers sit on this one work
Validation status
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Abstract

Graceful choreography for CO 2 and H 2 O One challenge for efficient electrochemical reduction of carbon dioxide (CO 2 ) is that the gas is hydrophobic, but many of its desirable reactions require water (H 2 O). García de Arquer et al. addressed this problem by combining a copper electrocatalyst with an ionomer assembly that intersperses sulfonate-lined paths for the H 2 O with fluorocarbon channels for the CO 2 . The electrode architecture enables production of two-carbon products such as ethylene and ethanol at current densities just over an ampere per square centimeter. Science , this issue p. 661

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The record

Venue
Science
Topic
CO2 Reduction Techniques and Catalysts
Field
Energy
Canadian institutions
University of New BrunswickUniversity of Toronto
Funders
Natural Sciences and Engineering Research Council of Canada
Keywords
ElectrolysisElectrolyteCatalysisMaterials scienceCarbonizationCopperInorganic chemistryChemical engineeringGas diffusion electrodeChemistryElectrodeMetallurgyComposite material
Has abstract in OpenAlex
yes