Consecutive Charging of a Perylene Bisimide Dye by Multistep Low‐Energy Solar‐Light‐Induced Electron Transfer Towards H₂ Evolution

Abstract

A photocatalytic system containing a perylene bisimide (PBI) dye as a photosensitizer anchored to titanium dioxide (TiO₂ ) nanoparticles through carboxyl groups was constructed. Under solar-light irradiation in the presence of sacrificial triethanolamine (TEOA) in neutral and basic conditions (pH 8.5), a reaction cascade is initiated in which the PBI molecule first absorbs green light, giving the formation of a stable radical anion (PBI^.- ), which in a second step absorbs near-infrared light, forming a stable PBI dianion (PBI^2- ). Finally, the dianion absorbs red light and injects an electron into the TiO₂ nanoparticle that is coated with platinum co-catalyst for hydrogen evolution. The hydrogen evolution rates (HERs) are as high as 1216 and 1022 μmol h^-1 g^-1 with simulated sunlight irradiation in neutral and basic conditions, respectively.