Immobilization of a Full Photosystem in the Large-Pore MIL-101 Metal-Organic Framework for CO2 reduction

Abstract

A molecular catalyst [Cp*Rh(4,4'-bpydc)]²⁺ and a molecular photosensitizer [Ru(bpy)₂ (4,4'-bpydc)]²⁺ (bpydc=bipyridinedicarboxylic acid) were co-immobilized into the highly porous metal-organic framework MIL-101-NH₂ (Al) upon easy postsynthetic impregnation. The Rh-Ru@MIL-101-NH₂ composite allows the reduction of CO₂ under visible light, while exhibiting remarkable selectivity with the exclusive production of formate. This Rh-Ru@MIL-101-NH₂ solid represents the first example of MOFs functionalized with both a catalyst and a photosensitizer in a noncovalent fashion. Thanks to the coconfinement of the catalyst and photosensitizer into the cavity's nanospace, the MOF pores are used as nanoreactors and enable molecular catalysis in a heterogeneous manner.

Keywords: carbon dioxide; heterogeneous catalysis; metal-organic frameworks; nanoreactors; photocatalysis.