Carbon dioxide capture underpins an important range of technologies that can help to mitigate climate change. Improved carbon capture technologies that are driven by electrochemistry are under active development, and it was recently found that supercapacitor energy storage devices can reversibly capture and release carbon dioxide. So-called supercapacitive swing adsorption (SSA) has several advantages over traditional carbon dioxide capture technologies such as lower energy consumption and the use of nontoxic materials. However, the mechanism for the capture of CO in these devices is poorly understood, making it challenging to design improved systems. Here, the mechanism of SSA is investigated via finite-element modeling with COMSOL of aqueous continuum transport equations, coupled to the CO to bicarbonate reaction. This simple computational model reproduces the key experimental observations and shows that charging leads to bicarbonate depletion (or accumulation) in the electrodes, driving CO capture (or release) at the gas-exposed electrode. This suggests that relevant aspects of the mechanism are captured without excluding other mechanisms that might be at play in parallel as well. At very low charging currents, both experiments and modeling reveal a decrease in the amount of carbon dioxide captured, suggesting the presence of competing processes at the two electrodes, and that SSA is an inherently kinetic phenomenon. This study highlights the importance of the operating conditions of these devices and may aid their development in the future.
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http://dx.doi.org/10.1021/acsnano.4c10931 | DOI Listing |
Int J Biol Macromol
January 2025
College of Materials Science and Engineering, Central South University of Forestry and Technology, Changsha 410004, PR China. Electronic address:
Microporous metal-organic frameworks (MOF) exhibit excellent carbon dioxide (CO) adsorption performance and selectivity for CO/N separation. However, the challenges associate with the recycling and reuse of MOF powders hinder their practical applications. To address these limitations, a flexible and stable MOF-based composite material was designed by immobilizing UiO-66(Zr)-(OH) onto cellulose nanofibers (CNFs) aerogels (MOF-CNFs), which featured high porosity.
View Article and Find Full Text PDFSci Rep
January 2025
Archaea Physiology & Biotechnology Group, Department of Functional and Evolutionary Ecology, University of Vienna, Wien, Austria.
Methanogenic archaea (methanogens) possess fascinating metabolic characteristics, such as the ability to fix molecular nitrogen (N). Methanogens are of biotechnological importance due to the ability to produce methane (CH) from molecular hydrogen (H) and carbon dioxide (CO) and to excrete proteinogenic amino acids. This study focuses on analyzing the link between biological methanogenesis and amino acid excretion under N-fixing conditions.
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January 2025
King Fahd University of Petroleum & Minerals, Dhahran, 31261, Saudi Arabia.
Climate change policies are driving the oil and gas industry to explore CO injection for carbon dioxide storage in reservoirs. In the United States, a substantial portion of oil production relies on CO-enhanced-oil-recovery (CO-EOR), demonstrating a growing interest in using CO to address various production challenges like condensate mitigation, pressure maintenance, and enhancing productivity in tight reservoirs. CO injection introduces gases like natural gas and N, either pre-existing or as impurities in the injected CO gas.
View Article and Find Full Text PDFNat Commun
January 2025
School of Mechatronical Engineering, Beijing Institute of Technology, Beijing, 100081, China.
Designing asymmetrical structures is an effective strategy to optimize metallic catalysts for electrochemical carbon dioxide reduction reactions. Herein, we demonstrate a transient pulsed discharge method for instantaneously constructing graphene-aerogel supports asymmetric copper nanocluster catalysts. This process induces the convergence of copper atoms decomposed by copper chloride onto graphene originating from the intense current pulse and high temperature.
View Article and Find Full Text PDFScience
January 2025
Redox and Metalloprotein Research Group, Max Planck Institute of Biophysics, Frankfurt am Main, Germany.
In the ancient microbial Wood-Ljungdahl pathway, carbon dioxide (CO) is fixed in a multistep process that ends with acetyl-coenzyme A (acetyl-CoA) synthesis at the bifunctional carbon monoxide dehydrogenase/acetyl-CoA synthase complex (CODH/ACS). In this work, we present structural snapshots of the CODH/ACS from the gas-converting acetogen , characterizing the molecular choreography of the overall reaction, including electron transfer to the CODH for CO reduction, methyl transfer from the corrinoid iron-sulfur protein (CoFeSP) partner to the ACS active site, and acetyl-CoA production. Unlike CODH, the multidomain ACS undergoes large conformational changes to form an internal connection to the CODH active site, accommodate the CoFeSP for methyl transfer, and protect the reaction intermediates.
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