z-logo
Premium
Consecutive Charging of a Perylene Bisimide Dye by Multistep Low‐Energy Solar‐Light‐Induced Electron Transfer Towards H 2 Evolution
Author(s) -
Xu Yucheng,
Zheng Jiaxin,
Lindner Joachim O.,
Wen Xinbo,
Jiang Nianqiang,
Hu Zhicheng,
Liu Linlin,
Huang Fei,
Würthner Frank,
Xie Zengqi
Publication year - 2020
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.202001231
Subject(s) - triethanolamine , photochemistry , perylene , photocatalysis , chemistry , titanium dioxide , photosensitizer , visible spectrum , electron transfer , platinum nanoparticles , catalysis , molecule , platinum , materials science , organic chemistry , optoelectronics , analytical chemistry (journal) , metallurgy
A photocatalytic system containing a perylene bisimide (PBI) dye as a photosensitizer anchored to titanium dioxide (TiO 2 ) 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 TiO 2 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.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom