State Key Laboratory of Photocatalysis on Energy and Environment, College of Chemistry, Fuzhou University, Fuzhou, 350002, P.R. China.
Max Planck Institute for Polymer Research, Ackermannweg 10, 55128, Mainz, Germany.
Angew Chem Int Ed Engl. 2016 Aug 1;55(32):9202-6. doi: 10.1002/anie.201603532. Epub 2016 Jun 15.
The search for metal-free organic photocatalysts for H2 production from water using visible light remains a key challenge. Reported herein is a molecular structural design of pure organic photocatalysts, derived from conjugated polybenzothiadiazoles, for photocatalytic H2 evolution using visible light. By alternating the substitution position of the electron-withdrawing benzothiadizole unit on the phenyl unit as a comonomer, various polymers with either one- or three-dimensional structures were synthesized and the effect of the molecular structure on their catalytic activity was investigated. Photocatalytic H2 evolution efficiencies up to 116 μmol h(-1) were observed by employing the linear polymer based on a phenyl-benzothiadiazole alternating main chain, with an apparent quantum yield (AQY) of 4.01 % at 420 nm using triethanolamine as the sacrificial agent.
寻找用于可见光分解水制氢的无金属有机光催化剂仍然是一个关键挑战。本文报道了一种纯有机光催化剂的分子结构设计,该光催化剂源自共轭聚苯并噻二唑,可用于可见光催化氢气的产生。通过改变作为共聚单体的苯环单元上吸电子苯并噻二唑单元的取代位置,可以合成具有一维或三维结构的各种聚合物,并研究了分子结构对其催化活性的影响。通过使用基于苯并噻二唑交替主链的线性聚合物,观察到高达 116 μmol h-1 的光催化氢气产生效率,在 420nm 下使用三乙醇胺作为牺牲剂时,表观量子产率(AQY)为 4.01%。