Real roles of perylene diimides for improving photocatalytic activity

Abstract

Three novel visible-light-driven composite photocatalysts: five-membered O-heterocyclic annulated perylene diimide doped TiO₂ (PDI-1/TiO₂), 1-phenol-<i>N</i>,<i>N</i>'-dicyclohexyl perylene-3,4,9,10-tetracarboxylic diimide doped TiO₂ (PDI-2/TiO₂), and <i>N</i>,<i>N</i>'-dicyclohexyl perylene diimide doped TiO₂ (PDI-3/TiO₂), were synthesized using a hydrothermal synthesis method. The effects of introducing PDIs with different structures into TiO₂ were evaluated by assaying the photodegradation rate of Methylene Blue (MB). The photoactivities of the PDI-1/TiO₂ and PDI-2/TiO₂ catalysts were better than that of PDI-3/TiO₂. This is because the large surface area of PDI-1 nanorods and PDI-2 nanobelts extended the 1D charge carrier channel, which facilitated electron transfer to the TiO₂ surface and improved the photocatalytic activity of the composites. The PDI-1/TiO₂ composite showed the highest photoactivity, and the activity remained at 86.4% after four reuse cycles. The extended π-π stacking of self-assembled PDI-1 and the strong interactions between self-assembled PDI-1 and TiO₂ played significant roles in accelerating charge transfer and decreasing recombination of photogenerated electron-hole pairs. The steric hindrance of the phenoxy substituent at the bay position of PDI-2 prevented the PDI-2 nucleus from contacting TiO₂ and weakened the interaction between PDI-2 and TiO₂, which further resulted in the low photoactivity of PDI-2/TiO₂. This work provides a practical way to improve the performances of traditional organic and inorganic composite photocatalysts.