An iron-porphyrin grafted metal–organic framework as a heterogeneous catalyst for the photochemical reduction of CO2

Photocatalytic reduction of carbon dioxide (CO2) into value-added carbon products is a promising strategy for dealing with carbon emission. Selected metal–organic frameworks (MOFs) have been shown promise in photocatalytic CO2 reduction owing to their photochemical activity and structural modularity. Here, we take advantage of displaceable nonstructural ligands on the nodes of a pyrene-based MOF, NU-1000, to graft a molecular catalyst, tetra(4-carboxyphenyl) porphyrin iron (III) chloride (Fe-TCPP). The pyrene linkers in the MOF absorb photons and transfer electrons to the porphyrin catalyst, resulting in a self-contained photocatalyst. The obtained Fe-TCPP@NU-1000 heterogeneous catalysts exhibit activity for CO2 photoreduction under illumination at 390 nm, with a TON for CO of 22 in 2 h. Molecular hydrogen is co-evolved. Leaching of the grafted catalyst from the MOF ultimately limits performance.