Iridium-Complexed Dipyridyl-Pyridazine Organosilica as a Catalyst for Water Oxidation

The heterogenization of metal-complex catalysts to be applied in water oxidation reactions is a currently growing field of great scientific impact for the development of energy conversion devices simulating the natural photosynthesis process. The attachment of IrCp*Cl complexes to the dipyridyl-pyridazine N-chelating sites on the surface of SBA-15 promotes the formation of metal bipyridine-like complexes, which can act as catalytic sites in the oxidation of water to dioxygen, the key half-reaction of artificial photosynthetic systems. The efficiency of the heterogeneous catalyst, Ir@NdppzSBA, in cerium(IV)-driven water oxidation was thoroughly evaluated, achieving high catalytic activity even at a long reaction time. The reusability and stability were also examined after three reaction cycles, with a slight loss of activity. A comparison with an analogous homogeneous iridium catalyst revealed the enhanced durability and performance of the heterogeneous system based on the Ir@NdppzSBA catalyst due to the stability of the SBA-15 structure as well as the isolated metal active sites. Thereby, this new versatile synthesis route for the preparation of water oxidation catalysts opens a new avenue for the construction of alternative heterogeneous catalytic systems with high surface area, ease of functionalization, and facile separation to improve the efficiency in the water oxidation reaction.