2020
DOI: 10.1039/d0ee01834a
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pH swing cycle for CO2capture electrochemically driven through proton-coupled electron transfer

Abstract: This study analyzes the energetic cost of CO2 separation using a pH swing created by electrochemical redox reactions of organic molecules involving PCET in aqueous electrolyte, and compares the experimental energetic cost to other methods.

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Cited by 97 publications
(158 citation statements)
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References 80 publications
(57 reference statements)
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“…As the proton‐coupled electron transfer reaction of phenazines in water influences the pH, the reduction potential of 1,6‐DPAP exhibits a pH‐dependent behavior (Supporting Information, Figure S31). The pH of the negolyte increased to 14 when the cell was fully charged, and went back to 8 when the cell was fully discharged, which was also observed in the previous literature [9d, 28] . The cell was cycled at a constant current density of 20 mA cm −2 for approximately 5.3 days and there was no obvious capacity fade observed.…”
Section: Resultssupporting
confidence: 82%
“…As the proton‐coupled electron transfer reaction of phenazines in water influences the pH, the reduction potential of 1,6‐DPAP exhibits a pH‐dependent behavior (Supporting Information, Figure S31). The pH of the negolyte increased to 14 when the cell was fully charged, and went back to 8 when the cell was fully discharged, which was also observed in the previous literature [9d, 28] . The cell was cycled at a constant current density of 20 mA cm −2 for approximately 5.3 days and there was no obvious capacity fade observed.…”
Section: Resultssupporting
confidence: 82%
“…Quinone chemistry has been typically used for CO 2 capture by PCET reactions ( Watkins et al., 2015 ). In 2020, sodium 3,3′-(phenazine-2,3-diylbis(oxy))bis(propane-1-sulfonate) (DSPZ) was studied as a redox-active organic proton carrier ( Jin et al., 2020 ). By utilizing the redox activity of 3,3'-(phenazine-2,3-diylbis(oxy))bis(propane-1-sulfonate) as a pH mediator, it was possible to capture CO 2 by forming an alkaline solution via the reduction of the redox molecule and to release CO 2 through acidification by re-oxidation.…”
Section: Electrochemical Gas Separationmentioning
confidence: 99%
“…148 Continued efforts will develop enhanced sorbents and processes that will capture more CO 2 per specic amount of sorbent, that are more stable, and that require less energy for desorption. [149][150][151][152][153][154][155] The present amount of captured CO 2 is on the order of 77 million tons a year, and only a small fraction of that is used in CDU processes. This is a far cry from where the activity level needs to be, based on climate models and business opportunities, as shown in Fig.…”
Section: Capture Of Carbon Dioxidementioning
confidence: 99%