摘要
In this paper, we describe efficient, inexpensive, and donor–acceptor (D–A) systems based on conjugated microporous polymers incorporating thiazolo[5,4-d]thiazole (ThTh) linkages for the extraction of H 2 from H 2 O under visible light in the presence of ascorbic acid (AA) as a sacrificial electron donor without additional noble metals as co-catalyst. The integration of electron-rich pyrene (Py) and electron-deficient ThTh units in Py-ThTh-CMP resulted in a D–A system that provided an H 2 evolution rate (HER) of 1874 µmol g –1 h −1 ; this value was greater than those of the other tested CMPs prepared with and without the ThTh acceptor moiety. Notably, Py-ThTh-CMP also exceeded the HERs of many other reported materials for photocatalytic H 2 O reduction, including co-catalysts based on covalent organic frameworks, CMPs, and graphitic carbon nitride. The DFT and TD-DFT suggested the incorporation of ThTh moiety in the CMPs backbone to enhance the charge transfer via S1 ↔ T1 and contribute to the H 2 formation. This study presents a new approach for preparing highly efficient photocatalysts for the practical development of cost-effective H 2 evolution.