Reactive capture of CO2 via amino acid

Reactive capture of carbon dioxide (CO<sub>2</sub>) offers an electrified pathway to produce renewable carbon monoxide (CO), which can then be upgraded into long-chain hydrocarbons and fuels. Previous reactive capture systems relied on hydroxide- or amine-based capture solutions. However, selectivity for CO remains low (<50%) for hydroxide-based systems and conventional amines are prone to oxygen (O<sub>2</sub>) degradation. Here, we develop a reactive capture strategy using potassium glycinate (K-GLY), an amino acid salt (AAS) capture solution applicable to O<sub>2</sub>-rich CO<sub>2</sub>-lean conditions. By employing a single-atom catalyst, engineering the capture solution, and elevating the operating temperature and pressure, we increase the availability of dissolved in-situ CO<sub>2</sub> and achieve CO production with 64% Faradaic efficiency (FE) at 50 mA cm<sup>-2</sup>. We report a measured CO energy efficiency (EE) of 31% and an energy intensity of 40 GJ t<sub>CO</sub><sup>-1</sup>, exceeding the best hydroxide- and amine-based reactive capture reports. The feasibility of the full reactive capture process is demonstrated with both simulated flue gas and direct air input.

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Publication Details

Journal
Nature Communications
Published
2024-09-08
DOI
https://doi.org/10.1038/s41467-024-51908-3
Citations
49
Primary Topic
CO2 Reduction Techniques and Catalysts
Type
article
Field-Weighted Citation Impact
5.02

Funders

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article

Reactive capture of CO2 via amino acid

Christine M. Gabardo, Yurou Celine Xiao, Paul J. Corbett, Mengyang Fan et al.
49 citations
Nature Communications
CO2 Reduction Techniques and Catalysts
5.02
article

Reactive capture of CO2 via amino acid

Christine M. Gabardo, Yurou Celine Xiao, Paul J. Corbett, Mengyang Fan, Chenyue Qiu, Jianan Erick Huang, Rui Kai Miao, Jane Y. Howe, Panagiotis Papangelakis, Geonhui Lee, Edward Hartley Sargent, Yuanjun Chen, Siyu Sonia Sun, Jiheon Kim, Zunmin Guo, Colin P. O’Brien, David Sinton, Kai Han, Yong Sheng Zhao, Feng Li, Xinyue Wang, Yan Yu
article en
49 citations

Abstract

Reactive capture of carbon dioxide (CO<sub>2</sub>) offers an electrified pathway to produce renewable carbon monoxide (CO), which can then be upgraded into long-chain hydrocarbons and fuels. Previous reactive capture systems relied on hydroxide- or amine-based capture solutions. However, selectivity for CO remains low (<50%) for hydroxide-based systems and conventional amines are prone to oxygen (O<sub>2</sub>) degradation. Here, we develop a reactive capture strategy using potassium glycinate (K-GLY), an amino acid salt (AAS) capture solution applicable to O<sub>2</sub>-rich CO<sub>2</sub>-lean conditions. By employing a single-atom catalyst, engineering the capture solution, and elevating the operating temperature and pressure, we increase the availability of dissolved in-situ CO<sub>2</sub> and achieve CO production with 64% Faradaic efficiency (FE) at 50 mA cm<sup>-2</sup>. We report a measured CO energy efficiency (EE) of 31% and an energy intensity of 40 GJ t<sub>CO</sub><sup>-1</sup>, exceeding the best hydroxide- and amine-based reactive capture reports. The feasibility of the full reactive capture process is demonstrated with both simulated flue gas and direct air input.

Nature CommunicationsVol. 15(1)
University of Toronto (CA), Shell (Netherlands) (NL)
Shell, Government of Ontario, Shell Global Solutions International, Canada Research Chairs, Natural Sciences and Engineering Research Council of Canada
Openalex Percentile: Top 3%
CO2 Reduction Techniques and Catalysts
5.02
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