Bioinspired cobalt cubanes with tunable redox potentials for photocatalytic water oxidation and CO(2) reduction

The development of efficient, robust and earth-abundant catalysts for photocatalytic conversions has been the Achilles’ heel of solar energy utilization. Here, we report on a chemical approach based on ligand designed architectures to fabricate unique structural molecular catalysts coupled with appropriate light harvesters (e.g., carbon nitride and Ru(bpy)(3)(2+)) for photoredox reactions. The “Co(4)O(4)” cubane complex Co(4)O(4)(CO(2)Me)(4)(RNC(5)H(4))(4) (R = CN, Br, H, Me, OMe), serves as a molecular catalyst for the efficient and stable photocatalytic water oxidation and CO(2) reduction. A comprehensive structure–function analysis emerged herein, highlights the regulation of electronic characteristics for a molecular catalyst by selective ligand modification. This work demonstrates a modulation method for fabricating effective, stable and earth-abundant molecular catalysts, which might facilitate further innovation in the function-led design and synthesis of cubane clusters for photoredox reactions.