Electrochemical Capture and Release of CO2 in Aqueous Electrolytes Using an Organic Semiconductor Electrode
Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide 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.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: CO2 Reduction Techniques and Catalysts · Covalent Organic Framework Applications · Carbon Dioxide Capture Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Faculty of Chemistry, University of Warsaw, 02-093 Warsaw, Poland
Institute of Physical Chemistry, University of Innsbruck, A-6020 Innsbruck, Austria
Department of Science and Technology, Linköpings Universitet, Campus Norrköping, SE-601 74 Norrköping, Sweden
Faculty of Chemistry, Warsaw University of Technology, 00-664 Warsaw, Poland
Funding
Austrian Science Fund · Politechnika Warszawska
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