Abstract
Polyoxometalates (POMs) are a diverse class of anionic metal-oxo clusters with intriguing chemical and physical properties. Owing to unrivaled versatility and structural variation, POMs have been extensively utilized for catalysis for a plethora of reactions. In this focused review, the applications of POMs as promising catalysts or co-catalysts for CO2 conversion, including CO2 photo/electro reduction and CO2 as a carbonyl source for the carbonylation process are summarized. A brief perspective on the potentiality in this field is proposed.
Highlights
As the main greenhouse gas produced by human activity, about 10 ± 0.5 gigatons CO2 were released in 2018, bringing the atmospheric CO2 concentration level over the threshold of 400 ppm [1].The large increase of global CO2 levels has led to serious environment problem
Most of POMs can be classified as Keggin, Wells-Dawson, Anderson-Evans, Silverton, Waugh, Strandberg, Lindqvist, and Peacock-Weakley type structures, which are named after their corresponding discoverers [7]
POMs stem from removing a variable number of {MO6 } octahedra from the plenary polyanion, resulting in metal-oxide clusters with vacant addenda metal sites. Such vacant sites can be treated as inorganic multidentate ligands (Figure 1) [10], For example, sandwich-type POMs are usually synthesized by the reaction of transition metal ions with appropriate lacunary POM precursors [5,8]
Summary
As the main greenhouse gas produced by human activity, about 10 ± 0.5 gigatons CO2 were released in 2018, bringing the atmospheric CO2 concentration level over the threshold of 400 ppm [1]. The large increase of global CO2 levels has led to serious environment problem It is the most abundant and nontoxic carbon resource for preparing useful compounds [2]. Most of POMs can be classified as Keggin, Wells-Dawson, Anderson-Evans, Silverton, Waugh, Strandberg, Lindqvist, and Peacock-Weakley type structures, which are named after their corresponding discoverers [7]. POMs stem from removing a variable number of {MO6 } octahedra from the plenary polyanion, resulting in metal-oxide clusters with vacant addenda metal sites Such vacant sites can be treated as inorganic multidentate ligands (Figure 1) [10], For example, sandwich-type POMs are usually synthesized by the reaction of transition metal ions with appropriate lacunary POM precursors [5,8].
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