Volume 63, Issue 51 e202412266
Research Article

Steering the Selectivity of CORR from Acetate to Ethanol via Tailoring the Thermodynamic Activity of Water

Jia Liu

Jia Liu

Department of Chemistry, 3 Science Drive 3, Singapore, 117543 Singapore

These authors contributed equally to this work.

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Bao Zhang

Bao Zhang

School of Materials and Energy, University of Electronic Science and Technology of China, Chengdu, 610054 Sichuan, China

These authors contributed equally to this work.

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Derong Chen

Derong Chen

Department of Chemistry, 3 Science Drive 3, Singapore, 117543 Singapore

Joint School of National University of Singapore and Tianjin University, International Campus of Tianjin University, Binhai New City, Fuzhou, 350207 China

These authors contributed equally to this work.

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Ouwen Peng

Ouwen Peng

Department of Chemistry, 3 Science Drive 3, Singapore, 117543 Singapore

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Haibin Ma

Haibin Ma

Department of Chemistry, 3 Science Drive 3, Singapore, 117543 Singapore

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Shibo Xi

Shibo Xi

Institute of Sustainability for Chemicals, Energy and Environment, A*STAR, Singapore

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Chao Wu

Chao Wu

Institute of Sustainability for Chemicals, Energy and Environment, A*STAR, Singapore

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Qikun Hu

Qikun Hu

Department of Chemistry, 3 Science Drive 3, Singapore, 117543 Singapore

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Kun Zhang

Kun Zhang

Department of Chemistry, 3 Science Drive 3, Singapore, 117543 Singapore

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Junyuan Feng

Junyuan Feng

Department of Chemistry, Southern University of Science and Technology, Shenzhen, Guangdong, 518000 P. R. China

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Kian Ping Loh

Corresponding Author

Kian Ping Loh

Department of Chemistry, 3 Science Drive 3, Singapore, 117543 Singapore

Joint School of National University of Singapore and Tianjin University, International Campus of Tianjin University, Binhai New City, Fuzhou, 350207 China

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First published: 19 August 2024
Citations: 4

Graphical Abstract

A universal approach was developed to tune the selectivity of Cu-based catalysts in CORR from acetate to ethanol by tailoring the thermodynamic activity of water. The faradaic efficiencies of ethanol and alcohol can reach 42.5 % and 55.1 % at 700 mA cm−2, respectively. The ability to control the selectivity of CORR opens up new possibilities for synthesizing a wider range of valuable chemical products from CO2.

Abstract

The electrochemical conversion of carbon monoxide (CO) into oxygenated C2+ products at high rates and selectivity offers a promising approach for the two-step conversion of carbon dioxide (CO2). However, a major drawback of the CO electrochemical reduction in alkaline electrolyte is the preference for the acetate pathway over the more valuable ethanol pathway. Recent research has shed light on the significant impact of thermodynamic water activity on the electrochemical CO2 reduction reaction pathways, but less is understood for the electrochemical reduction of CO. In this study, we investigated how the water activity at the electrified interface can be enhanced to adjust the selectivity between acetate and ethanol. We employed an ionomer modifier to lower the local concentration of alkali ions (via Donnan exclusion), successfully enhancing ethanol production while suppressing acetate formation. We observed a remarkable improvement in the Faradaic efficiency of ethanol and alcohol (i. e. ethanol, propanol etc), which reached 42.5 % and 55.1 %, respectively, at a current density of 700 mA cm−2. The partial current densities of ethanol and alcohol reached 698 and 942 mA cm−2 at 2000 mA cm−2. Furthermore, we achieved a 3.7-fold increase in the ethanol/acetate ratio, providing clear evidence of our successful modulation of product selectivity.

Conflict of Interests

The authors declare no competing financial interests.

Data Availability Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.

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