Currently, photochemical carbon dioxide reduction is a most sought‐after process as it involves the simultaneous removal of greenhouse CO2 gas and the production of useful products. In this study, we report the selective formation of formaldehyde in photochemical carbon dioxide reduction using a reduced polyoxometalate (POM) based catalyst. By simply tuning the redox state of the metal centre in the POM, we can obtain the more reduced product formaldehyde from carbon dioxide. As a result of the high MoV/MoVI ratio in the cluster, formaldehyde is obtained as the major product as opposed to formic acid. Since the catalyst POM 1 itself readily absorbs light, no external photosensitizer is used. In the reduction process of carbon dioxide, water acts as the electron donor and is oxidized to oxygen rendering the whole process viable and green. (1=Mo16=[{(CH3)NH2}4{(MoV2O4)6(μ2‐OH)10(μ2‐O)2(μ3‐OH)2(μ3‐O)2(MoVIO3H)4}]0.94[{(MoV2O4)6(μ2‐OH)10(μ2‐O)2(MoVIO3H)4}{MoVI(μ3‐O)4}]0.06).
A soft-oxometalate (SOM) based on Mo and V i.e. {MoV} in their highest oxidation state reduces CO to HCOOH selectively in water. Catalysis initiates without the use of any photosensitizer and solvent water acts as the sacrificial electron donor which gets oxidized to generate oxygen. Electrons and protons released in this process reduce CO to HCOOH.
Correction for ‘Selective light driven reduction of CO2 to HCOOH in water using a {MoV9}n (n = 1332–3600) based soft-oxometalate (SOM)’ by Soumitra Barman et al., Chem. Commun., 2018, 54, 2369–2372, DOI: 10.1039/C7CC09520A.
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