Open AccessEfficient Photoinduced Electron Transfer from Pyrene‐ o ‐Carborane Heterojunction to Selenoviologen for Enhanced Photocatalytic Hydrogen Evolution and Reduction of Alkynes
Author(s) -
Yang Xiaodong,
Zhang Bingjie,
Gao Yujing,
Liu Chenjing,
Li Guoping,
Rao Bin,
Chu Dake,
Yan Ni,
Zhang Mingming,
He Gang
Publication year - 2022
Publication title -
advanced science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.388
H-Index - 100
ISSN - 2198-3844
DOI - 10.1002/advs.202101652
Subject(s) - pyrene , photochemistry , photoinduced electron transfer , photocatalysis , chemistry , electron transfer , intramolecular force , supramolecular assembly , electron donor , electrochromism , catalysis , supramolecular chemistry , materials science , stereochemistry , organic chemistry , electrode , molecule
A series of pyrene or pyrene‐ o ‐carborane‐appendant selenoviologens (Py‐SeV 2+ , Py‐Cb‐SeV 2+ ) 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 (SeV 2+ ) ( k ET = 1.2 × 10 10 s −1 ) endows the accelerating the generation of selenoviologen radical cation (SeV +• ) compared with Py‐SeV 2+ and other derivatives. The electrochromic/electrofluorochromic devices’ (ECD and EFCD) measurements and supramolecular assembly/disassembly processes of SeV 2+ 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‐SeV 2+ ‐based system shows high‐efficiency visible‐light‐driven HER and highly selective phenylacetylene reduction due to the efficient PET process.