Maryam Abdinejad*, Mathilde Reffet, Kai-Jher Tan and T. Alan Hatton*,
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Sustainable Electrochemical CO2 Capture from Air Using Heterogenized Quinones in Aqueous Media
The urgent need to mitigate rising carbon dioxide (CO2) emissions necessitates the development of innovative and sustainable carbon capture technologies. This study introduces a dual-electrode electrochemically mediated CO2 capture system, employing the heterogenization of the redox-active polymerized benzodithiophene quinone (PBDT-Q) immobilized onto carbon nanotubes (CNTs) to form a PBDT-Q/CNT composite. The heterogenization improves the composite’s structural stability, conductivity, and enabling prolonged operation in an environmentally friendly aqueous medium. We initiated a systematic evaluation with a bulk electrolyzer, demonstrating efficient CO2 capture and release. Subsequently, we expanded the investigation to a flow-cell system tested with a simulated flue gas mixture containing 13 vol % CO2 and 3.5 vol % O2. The flow-cell system maintained stable performance over 68 cycles spanning 150 h, achieving an average capture rate of approximately 0.21 mmol CO2 per cycle. These results underscore the scalability and real-world potential of dual-electrode heterogenized quinone-based electrocatalysts, offering a sustainable pathway to advance carbon capture technologies.
期刊介绍:
ACS Sustainable Chemistry & Engineering is a prestigious weekly peer-reviewed scientific journal published by the American Chemical Society. Dedicated to advancing the principles of green chemistry and green engineering, it covers a wide array of research topics including green chemistry, green engineering, biomass, alternative energy, and life cycle assessment.
The journal welcomes submissions in various formats, including Letters, Articles, Features, and Perspectives (Reviews), that address the challenges of sustainability in the chemical enterprise and contribute to the advancement of sustainable practices. Join us in shaping the future of sustainable chemistry and engineering.