TY - JOUR
T1 - The carbon dioxide radical anion as a reductant in water treatment and atmospheric chemistry
T2 - a review
AU - Schaefer, Thomas
AU - Raff, Jonathan D.
AU - Nadagouda, Mallikarjuna N.
AU - Lichtfouse, Eric
AU - Meyerstein, Dan
AU - Herrmann, Hartmut
AU - Sharma, Virender K.
N1 - Publisher Copyright:
© The Author(s) 2026.
PY - 2026
Y1 - 2026
N2 - The carbon dioxide radical anion, CO2●−, is a highly reactive radical species involved in the reduction of the CO2 greenhouse gas, organic synthesis, atmospheric aerosol chemistry, and treatment of halogenated compounds. In recent years, CO2●− has emerged as a strong reductant, or single electron donor. Here we present techniques used to generate CO2●− and we discuss applications to degrading pollutants such as halogenated alkanes. The potential occurrence of such reductions in water and aqueous aerosols is discussed, notably for the degradation of perfluoroalkyl substances. In the laboratory, CO2●− is directly generated by either direct electrochemical reduction of CO2 or hydrogen atom transfer of either formate salts with and without catalysts or ferrioxalate through photochemical or radiolytic processes. The CO2●− has an ultraviolet spectrum, and CO2●− vibration modes are characterized by fast kinetics using infrared and Raman spectroscopy. The second-order rate constants of the reactions of CO2●− with halogenated alkanes, of -1.84 ± 0.22 V, are generally slower than that of the hydrated electron, of -2.87 V, and give a negative linear relationship with energy of lower unoccupied molecular orbital, suggesting single electron transfer mechanism in reducing the halogenated compounds.
AB - The carbon dioxide radical anion, CO2●−, is a highly reactive radical species involved in the reduction of the CO2 greenhouse gas, organic synthesis, atmospheric aerosol chemistry, and treatment of halogenated compounds. In recent years, CO2●− has emerged as a strong reductant, or single electron donor. Here we present techniques used to generate CO2●− and we discuss applications to degrading pollutants such as halogenated alkanes. The potential occurrence of such reductions in water and aqueous aerosols is discussed, notably for the degradation of perfluoroalkyl substances. In the laboratory, CO2●− is directly generated by either direct electrochemical reduction of CO2 or hydrogen atom transfer of either formate salts with and without catalysts or ferrioxalate through photochemical or radiolytic processes. The CO2●− has an ultraviolet spectrum, and CO2●− vibration modes are characterized by fast kinetics using infrared and Raman spectroscopy. The second-order rate constants of the reactions of CO2●− with halogenated alkanes, of -1.84 ± 0.22 V, are generally slower than that of the hydrated electron, of -2.87 V, and give a negative linear relationship with energy of lower unoccupied molecular orbital, suggesting single electron transfer mechanism in reducing the halogenated compounds.
KW - Carbon dioxide radical anion
KW - Degradation
KW - Electron transfer
KW - Kinetics
KW - Mechanism
KW - PFAS
KW - Reduction
UR - https://www.scopus.com/pages/publications/105028867301
U2 - 10.1007/s10311-025-01894-9
DO - 10.1007/s10311-025-01894-9
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AN - SCOPUS:105028867301
SN - 1610-3653
JO - Environmental Chemistry Letters
JF - Environmental Chemistry Letters
ER -