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Abstract The unprecedented increase in atmospheric CO 2 concentration calls for effective carbon capture technologies. With distributed sources contributing to about half of the overall emission, CO 2 capture from the atmosphere direct air capture, (DAC) is more relevant than ever. Herein, an electrochemically mediated DAC system is reported which utilizes affinity of redox‐active quinone moieties towards CO 2 molecules, and unlike incumbent chemisorption technologies which require temperature or pH swing, relies solely on the electrochemical voltage for CO 2 capture and release. The design and operation of a DAC system is demonstrated with stackable bipolar cells using quinone chemistry. Specifically, poly(vinylanthraquinone) (PVAQ) negative electrode undergoes a two‐electron reduction reaction and reversibly complexes with CO 2 , leading to CO 2 sequestration from the feed stream. The subsequent PVAQ oxidation, conversely, results in release of CO 2 . The performance of both small‐ and meso‐scale cells for DAC are evaluated with feed CO 2 concentrations as low as 400 ppm (0.04 %), and energy consumption is demonstrated as low as 113 kJ per mole of CO 2 captured. Notably, the bipolar cell construct is modular and expandable, equally suitable for small and large plants. Moving forward, this work presents a viable and highly customizable electrochemical method for DAC.
Hemmatifar et al. (Fri,) studied this question.