Unprecedented metal-free photocatalytic CO conversion to CO (up to 228±48 μmol g h) was displayed by TiO@IL hybrid photocatalysts prepared by simple impregnation of commercially available P25-titanium dioxide with imidazolium-based ionic liquids (ILs). The high activity of TiO@IL hybrid photocatalysts was mainly associated to (i) TiO@IL red shift compared to the pure TiO absorption, and thus a modification of the TiO surface electronic structure; (ii) TiO with IL bearing imidazolate anions lowered the CO activation energy barrier. The reaction mechanism was postulated to occur via CO photoreduction to formate species by the imidazole/imidazole radical redox pair, yielding CO and water.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7692890 | PMC |
http://dx.doi.org/10.1002/cssc.202001717 | DOI Listing |
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