Electrochemical Capture and Release of CO2 in Aqueous Electrolytes Using an Organic Semiconductor Electrode
Author(s) -
Doğukan Hazar Apaydın,
Monika Góra,
Engelbert Portenkirchner,
Kerstin Oppelt,
Helmut Neugebauer,
Marie Jakešová,
Eric Daniel Głowacki,
Julia KunzeLiebhäuser,
Małgorzata Zagórska,
Józef Mieczkowski,
Niyazi Serdar Sariçiftçi
Publication year - 2017
Publication title -
acs applied materials and interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.535
H-Index - 228
eISSN - 1944-8252
pISSN - 1944-8244
DOI - 10.1021/acsami.7b01875
Subject(s) - materials science , electrochemistry , aqueous solution , dissolution , electrolyte , electrochemical reduction of carbon dioxide , amine gas treating , carbon dioxide , electrode , carbon dioxide sensor , organic semiconductor , inorganic chemistry , chemical engineering , catalysis , organic chemistry , chemistry , carbon monoxide , optoelectronics , engineering
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.
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