Catalytic Space Engineering of Porphyrin Metal-Organic Frameworks for Combined CO2 Capture and Conversion at a Low Concentration

Abstract

Porous porphyrin metal-organic frameworks (PMOFs) provide promising platforms for studying CO₂ capture and conversion (C3) owing to their versatility in photoelectric, catalytic, and redox activities and porphyrin coordination chemistry. Herein, we report the C3 application of two PMOFs by engineering the coordination space through the introduction of two catalytic metalloporphyrins doped with rhodium or iridium, Rh-PMOF-1 and Ir-PMOF-1, both of which can serve as heterogeneous catalysts for the chemical fixation of CO₂ into cyclic carbonates with yields of up to 99 %. Remarkably, the catalytic reactions can effectively proceed under low CO₂ concentrations and high yields of 83 % and 73 % can be obtained under 5 % CO₂ in the presence of Rh-PMOF-1 and Ir-PMOF-1, respectively. The synergistic effect of the metalloporphyrin ligand and the Zr₆ O₈ cluster, in combination with the CO₂ concentration effect from the pore space, might account for the excellent catalytic performance of Rh-PMOF-1 under low CO₂ concentration. Recycling tests of Rh-PMOF-1 show negligible loss of catalytic activity after 10 runs.

Keywords: carbon dioxide capture; heterogeneous catalysis; metal-organic frameworks; rhodium porphyrin; synergistic effects.