Enhancing electrochemical carbon dioxide capture with supercapacitors

被引:1
|
作者
Zhen Xu
Grace Mapstone
Zeke Coady
Mengnan Wang
Tristan L. Spreng
Xinyu Liu
Davide Molino
Alexander C. Forse
机构
[1] University of Cambridge,Yusuf Hamied Department of Chemistry
[2] Imperial College London,Department of Chemical Engineering
[3] Dipartimento di Scienza Applicata e Tecnologia (DISAT),Politecnico di Torino
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D O I
10.1038/s41467-024-52219-3
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摘要
Supercapacitors are emerging as energy-efficient and robust devices for electrochemical CO2 capture. However, the impacts of electrode structure and charging protocols on CO2 capture performance remain unclear. Therefore, this study develops structure-property-performance correlations for supercapacitor electrodes at different charging conditions. We find that electrodes with large surface areas and low oxygen functionalization generally perform best, while a combination of micro- and mesopores is important to achieve fast CO2 capture rates. With these structural features and tunable charging protocols, YP80F activated carbon electrodes show the best CO2 capture performance with a capture rate of 350 mmolCO2 kg–1 h–1 and a low electrical energy consumption of 18 kJ molCO2–1 at 300 mA g–1 under CO2, together with a long lifetime over 12000 cycles at 150 mA g–1 under CO2 and excellent CO2 selectivity over N2 and O2. Operated in a “positive charging mode”, the system achieves excellent electrochemical reversibility with Coulombic efficiencies over 99.8% in the presence of approximately 15% O2, alongside stable cycling performance over 1000 cycles. This study paves the way for improved supercapacitor electrodes and charging protocols for electrochemical CO2 capture.
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