Supercapacitive swing adsorption (SSA) is a recently discovered electrochemically driven CO capture technology that promises significant efficiency improvements over traditional methods. A limitation of this approach is the relatively low CO adsorption capacity, and the underlying molecular mechanisms of SSA remain poorly understood, hindering optimization. Here we present a new device architecture for simultaneous electrochemical and gas-adsorption measurements, and use it to investigate the effects of charging protocols on SSA performance. We show that altering the voltage applied to charge the SSA device can significantly improve performance. Charging the gas-exposed electrode positively rather than negatively increases CO adsorption capacity and causes CO desorption rather than adsorption with charging. We also show that switching the voltage between positive and negative values further increases CO capacity. Previously proposed mechanisms of the SSA effect fail to explain these phenomena, so we present a new mechanism based on movement of CO-derived species into and out of electrode micropores. Overall, this work advances our knowledge of electrochemical CO adsorption by supercapacitors, potentially leading to devices with increased uptake capacity and efficiency.
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http://dx.doi.org/10.1039/d2nr00748g | DOI Listing |
Angew Chem Int Ed Engl
September 2024
Department of Chemistry, Lehigh University, 6 East Packer Avenue, Bethlehem, PA 18015, USA.
We report on the supercapacitive swing adsorption (SSA) of carbon dioxide at different voltage windows in the presence of oxygen using activated carbon electrodes, and deliquescent, aqueous electrolytes. The presence of O in the CO/N gas mixture results in an up to 11 times higher CO adsorption capacity with 3 M MgBr (at 0.6 V) and up to 4-5 times higher adsorption capacity with 3 M MgCl (at 1 V).
View Article and Find Full Text PDFSmall
August 2024
Department of Chemistry, Lehigh University, 6 East Packer Avenue, Bethlehem, PA, 18015, USA.
Supercapacitive swing adsorption (SSA) modules with bipolar stacks having 2, 4, 8, and 12 electrode pairs made from BPL 4 × 6 activated carbon are constructed and tested for carbon dioxide capture applications. Tests are performed with simulated flue gas (15%CO /85%N) at 2, 4, 8, and 12 V, respectively. Reversible adsorption with sorption capacities (≈58 mmol kg) and adsorption rates (≈38 µmol kg s) are measured for all stacks.
View Article and Find Full Text PDFSmall
June 2023
Department of Chemistry, 6 East Packer Avenue, Lehigh University, Bethlehem, PA, 18015, USA.
Supercapacitive swing adsorption (SSA) with garlic roots-derived activated carbon achieves a record adsorption capacity of 312 mmol kg at a low energy consumption of 72 kJ mol and high mass loadings (>30 mg cm ) at 1.0 V for 85%N /15%CO mixtures. The activated carbons are inexpensively prepared in a one-step process using potassium carbonate, and air as activators.
View Article and Find Full Text PDFNanoscale
June 2022
Department of Chemistry, University of Cambridge, Lensfield Road, CB2 1EW, UK.
Supercapacitive swing adsorption (SSA) is a recently discovered electrochemically driven CO capture technology that promises significant efficiency improvements over traditional methods. A limitation of this approach is the relatively low CO adsorption capacity, and the underlying molecular mechanisms of SSA remain poorly understood, hindering optimization. Here we present a new device architecture for simultaneous electrochemical and gas-adsorption measurements, and use it to investigate the effects of charging protocols on SSA performance.
View Article and Find Full Text PDFACS Appl Mater Interfaces
June 2019
Department of Chemistry , Lehigh University, 6 East Packer Avenue , Bethlehem , Pennsylvania 18015 , United States.
We quantitatively investigate the influence of the NaCl electrolyte concentration on the adsorptive and energetic characteristics of supercapacitive swing adsorption (SSA) for the separation of CO from a simulated flue gas mixture containing 15% CO and 85% N. The investigated concentrations were that of deionized water, 0.010, 0.
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