Efficient Photoinduced Electron Transfer from Pyrene-o-Carborane Heterojunction to Selenoviologen for Enhanced Photocatalytic Hydrogen Evolution and Reduction of Alkynes.

ABSTRACT

A series of pyrene or pyrene-o-carborane-appendant selenoviologens (Py-SeV2+ , Py-Cb-SeV2+ ) for enhanced photocatalytic hydrogen evolution reaction (HER) and reduction of alkynes is reported. The efficient photoinduced electron transfer (PET) from electron-rich pyrene-o-carborane heterojunction (Py-Cb) with intramolecular charge transfer (ICT) characteristic to electron-deficient selenoviologen (SeV2+ ) (kET = 1.2 × 1010 s-1 ) endows the accelerating the generation of selenoviologen radical cation (SeV+• ) compared with Py-SeV2+ and other derivatives. The electrochromic/electrofluorochromic devices' (ECD and EFCD) measurements and supramolecular assembly/disassembly processes of SeV2+ and cucurbit[8]uril (CB[8]) results show that the PET process can be finely tuned by electrochemical and host-guest chemistry methods. By combination with Pt-NPs catalyst, the Py-Cb-SeV2+ -based system shows high-efficiency visible-light-driven HER and highly selective phenylacetylene reduction due to the efficient PET process.