Selective and Energy Efficient Electrocatalytic CO2‐to‐Ethanol Conversion through Anion Modulation
Ethanol, with its high market value and stable global demand, stands out as an attractive product of electrocatalytic CO2 reduction. However, achieving high ethanol selectivity and energy efficiency at industrial current densities remains challenging. In this study, we employed a blended anion modul...
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Published in | Angewandte Chemie International Edition Vol. 64; no. 35; pp. e202506867 - n/a |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
Wiley Subscription Services, Inc
25.08.2025
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Edition | International ed. in English |
Subjects | |
Online Access | Get full text |
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Summary: | Ethanol, with its high market value and stable global demand, stands out as an attractive product of electrocatalytic CO2 reduction. However, achieving high ethanol selectivity and energy efficiency at industrial current densities remains challenging. In this study, we employed a blended anion modulation strategy to enhance the selectivity and energy efficiency of CO2‐to‐ethanol conversion. The Cu2(OH)3F pre‐catalyst achieved Faradaic efficiencies of 50% and 93% for ethanol and C2+, respectively, at 700 mA cm−2 in a blended electrolyte consisting of 2 M KOH and 1 M KCl. Comprehensive electrochemical tests, combined with in situ characterizations and theoretical analysis, revealed that chloride and hydroxide increased *CO coverage for efficient C─C coupling. Moreover, hydroxide stabilizes the *CHCOH intermediate through hydrogen bonding with the adsorbed hydroxide on the catalyst surface, while Cl synergistically enhances its reactivity by promoting water dissociation toward the ethanol pathway.
We employed blended OH− and Cl− electrolyte to alter the electrocatalytic CO2 reduction microenvironment, achieving ethanol faradaic efficiency of 50% at 700 mA cm−2. The blended anions cooperatively promoted ethanol production by increasing *CO coverage and modulating the reactivity of key branching intermediate *CHCOH. |
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Bibliography: | Both authors contributed equally to this work. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 1433-7851 1521-3773 1521-3773 |
DOI: | 10.1002/anie.202506867 |