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CO2-mediated organocatalytic chlorine evolution under industrial conditions
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CO2-mediated organocatalytic chlorine evolution under industrial conditions
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CO2-mediated organocatalytic chlorine evolution under industrial conditions
CO2-mediated organocatalytic chlorine evolution under industrial conditions
Journal Article

CO2-mediated organocatalytic chlorine evolution under industrial conditions

2023
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Overview
During the chlor-alkali process, in operation since the nineteenth century, electrolysis of sodium chloride solutions generates chlorine and sodium hydroxide that are both important for chemical manufacturing 1 – 4 . As the process is very energy intensive, with 4% of globally produced electricity (about 150 TWh) going to the chlor-alkali industry 5 – 8 , even modest efficiency improvements can deliver substantial cost and energy savings. A particular focus in this regard is the demanding chlorine evolution reaction, for which the state-of-the-art electrocatalyst is still the dimensionally stable anode developed decades ago 9 – 11 . New catalysts for the chlorine evolution reaction have been reported 12 , 13 , but they still mainly consist of noble metal 14 – 18 . Here we show that an organocatalyst with an amide functional group enables the chlorine evolution reaction; and that in the presence of CO 2 , it achieves a current density of 10 kA m −2 and a selectivity of 99.6% at an overpotential of only 89 mV and thus rivals the dimensionally stable anode. We find that reversible binding of CO 2 to the amide nitrogen facilitates formation of a radical species that plays a critical role in Cl 2 generation, and that might also prove useful in the context of Cl − batteries and organic synthesis 19 – 21 . Although organocatalysts are typically not considered promising for demanding electrochemical applications, this work demonstrates their broader potential and the opportunities they offer for developing industrially relevant new processes and exploring new electrochemical mechanisms. A study shows that an organocatalyst with an amide functional group, and carbon dioxide, can efficiently and selectively produce chlorine, potentially offering a low-cost and less energy intensive alternative to the chlor-alkali process.