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Oxygen-Stable Electrochemical CO2 Capture using Redox-Active Heterocyclic Benzodithiophene Quinone

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Angew Chem Int Ed - 2024 - Abdinejad - Oxygen‐Stable Electrochemical CO2 Capture using Redox‐Active Heterocyclic.pdf

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sword-2025-08-04T20:49:38.original.xml (130 B)
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Author(s)
Abdinejad, Maryam
•
Massen‐Hane, Michael
•
Seo, Hyowon
•
Hatton, T Alan
Date Issued
September 9, 2024
Journal
Angewandte Chemie International Edition
Publisher
Wiley
Citation
Abdinejad, Maryam, Massen‐Hane, Michael, Seo, Hyowon and Hatton, T Alan. 2024. "Oxygen-Stable Electrochemical CO2 Capture using Redox-Active Heterocyclic Benzodithiophene Quinone." Angewandte Chemie International Edition, 63 (52).
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Final published version
Abstract
Electrochemical carbon capture offers a promising alternative to thermal amine technology, which serves as the traditional benchmark method for CO2 capture. Despite its technological maturity, the widespread deployment of thermal amine technologies is hindered by high energy consumption and sorbent degradation. In contrast, electrochemical methods, with their inherently isothermal operation, address these challenges, offering enhanced energy efficiency and robustness. Among emerging strategies, electrochemical carbon capture systems using redox-active materials such as quinones stand out for their potential to capture CO2. However, their practical application is currently limited by their low stability in the presence of oxygen. We demonstrate that benzodithiophene quinone (BDT-Q), a heterocyclic quinone, exhibits high stability in electrochemical carbon capture processes with oxygen-containing feed gas. Conducted in a cyclic flow system with a simulated flue gas mixture containing 13 % CO2 and 3.5 % O2 for over 100 hours, the process demonstrates high oxygen stability with an electron utilization of 0.83 without significant degradation, indicating a promising approach for real world applications. Our study explores the potential of new heterocyclic quinone compounds in the context of carbon capture technologies.
MIT Department
Massachusetts Institute of Technology. Department of Chemical Engineering
Terms of Use
Creative Commons Attribution-NonCommercial-NoDerivatives
https://creativecommons.org/licenses/by-nc-nd/4.0/
Persistent DSpace Link
https://hdl.handle.net/1721.1/162193
DOI of Published Version
https://doi.org/10.1002/anie.202412229
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