Molecular Photocatalytic Water Splitting by Mimicking Photosystems I and II

In nature, water is oxidized by plastoquinone to evolve O₂ and form plastoquinol in Photosystem II (PSII), whereas NADP⁺ is reduced by plastoquinol to produce NADPH and regenerate plastoquinone in Photosystem I (PSI), using homogeneous molecular photocatalysts. However, water splitting to evolve H₂ and O₂ in a 2:1 stoichiometric ratio has yet to be achieved using homogeneous molecular photocatalysts, remaining as one of the biggest challenges in science. Herein, we demonstrate overall water splitting to evolve H₂ and O₂ in a 2:1 ratio using a two liquid membranes system composed of two toluene phases, which are separated by a solvent mixture of water and trifluoroethanol (H₂O/TFE, 3:1 v/v), with a glass membrane to combine PSI and PSII molecular models. A PSII model contains plastoquinone analogs [p-benzoquinone derivatives (X-Q)] in toluene and an iron(II) complex as a molecular oxidation catalyst in H₂O/TFE (3:1 v/v), which evolves a stoichiometric amount of O₂ and forms plastoquinol analogs (X-QH₂) under photoirradiation. On the other hand, a PSI model contains nothing in toluene but contains X-QH₂, 9-mesityl-10-methylacridinium ion (Acr⁺-Mes) as a photocatalyst, and a cobalt(III) complex as an H₂ evolution catalyst in H₂O/TFE (3:1 v/v), which evolves a stoichiometric amount of H₂ and forms X-Q under photoirradiation. When a PSII model system is combined with a PSI model system with two glass membranes and two liquid membranes, photocatalytic water splitting with homogeneous molecular photocatalysts is achieved to evolve hydrogen and oxygen with the turnover number (TON) of >100.