Immobilization strategies for porphyrin-based molecular catalysts for the electroreduction of CO

The ever-growing level of carbon dioxide (CO 2 ) in our atmosphere, is at once a threat and an opportunity. The development of sustainable and cost-effective pathways to convert CO 2 to value-added chemicals is central to reducing its atmospheric presence. Electrochemical CO 2 reduction reactions (C...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2022-04, Vol.1 (14), p.7626-7636
Hauptverfasser: Abdinejad, Maryam, Tang, Keith, Dao, Caitlin, Saedy, Saeed, Burdyny, Tom
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Zusammenfassung:The ever-growing level of carbon dioxide (CO 2 ) in our atmosphere, is at once a threat and an opportunity. The development of sustainable and cost-effective pathways to convert CO 2 to value-added chemicals is central to reducing its atmospheric presence. Electrochemical CO 2 reduction reactions (CO 2 RRs) driven by renewable electricity are among the most promising techniques to utilize this abundant resource; however, in order to reach a system viable for industrial implementation, continued improvements to the design of electrocatalysts is essential to improve the economic prospects of the technology. This review summarizes recent developments in heterogeneous porphyrin-based electrocatalysts for CO 2 capture and conversion. We specifically discuss the various chemical modifications necessary for different immobilization strategies, and how these choices influence catalytic properties. Although a variety of molecular catalysts have been proposed for CO 2 RRs, the stability and tunability of porphyrin-based catalysts make their use particularly promising in this field. We discuss the current challenges facing CO 2 RRs using these catalysts and our own solutions that have been pursued to address these hurdles. Using homogeneous and heterogeneous metalloporphyrin-based catalysts for electroreduction of CO 2 to value-added materials.
ISSN:2050-7488
2050-7496
DOI:10.1039/d2ta00876a