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Electrochemical Capture and Release of CO(2) in Aqueous Electrolytes Using an Organic Semiconductor Electrode

[Image: see text] Developing efficient methods for capture and controlled release of carbon dioxide is crucial to any carbon capture and utilization technology. Herein we present an approach using an organic semiconductor electrode to electrochemically capture dissolved CO(2) in aqueous electrolytes...

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Detalles Bibliográficos
Autores principales: Apaydin, Dogukan H., Gora, Monika, Portenkirchner, Engelbert, Oppelt, Kerstin T., Neugebauer, Helmut, Jakesova, Marie, Głowacki, Eric D., Kunze-Liebhäuser, Julia, Zagorska, Malgorzata, Mieczkowski, Jozef, Sariciftci, Niyazi Serdar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399472/
https://www.ncbi.nlm.nih.gov/pubmed/28378994
http://dx.doi.org/10.1021/acsami.7b01875
Descripción
Sumario:[Image: see text] Developing efficient methods for capture and controlled release of carbon dioxide is crucial to any carbon capture and utilization technology. Herein we present an approach using an organic semiconductor electrode to electrochemically capture dissolved CO(2) in aqueous electrolytes. The process relies on electrochemical reduction of a thin film of a naphthalene bisimide derivative, 2,7-bis(4-(2-(2-ethylhexyl)thiazol-4-yl)phenyl)benzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetraone (NBIT). This molecule is specifically tailored to afford one-electron reversible and one-electron quasi-reversible reduction in aqueous conditions while not dissolving or degrading. The reduced NBIT reacts with CO(2) to form a stable semicarbonate salt, which can be subsequently oxidized electrochemically to release CO(2). The semicarbonate structure is confirmed by in situ IR spectroelectrochemistry. This process of capturing and releasing carbon dioxide can be realized in an oxygen-free environment under ambient pressure and temperature, with uptake efficiency for CO(2) capture of ∼2.3 mmol g(–1). This is on par with the best solution-phase amine chemical capture technologies available today.