| Literature DB >> 31989745 |
Mi Zhang1, Meng Lu1, Zhong-Ling Lang2, Jiang Liu1, Ming Liu1, Jia-Nan Chang1, Le-Yan Li1, Lin-Jie Shang1, Min Wang1, Shun-Li Li1, Ya-Qian Lan1.
Abstract
A strategy to covalently connect crystalline covalent organic frameworks (COFs) with semiconductors to create stable organic-inorganic Z-scheme heterojunctions for artificial photosynthesis is presented. A series of COF-semiconductor Z-scheme photocatalysts combining water-oxidation semiconductors (TiO2 , Bi2 WO6 , and α-Fe2 O3 ) with CO2 reduction COFs (COF-316/318) was synthesized and exhibited high photocatalytic CO2 -to-CO conversion efficiencies (up to 69.67 μmol g-1 h-1 ), with H2 O as the electron donor in the gas-solid CO2 reduction, without additional photosensitizers and sacrificial agents. This is the first report of covalently bonded COF/inorganic-semiconductor systems utilizing the Z-scheme applied for artificial photosynthesis. Experiments and calculations confirmed efficient semiconductor-to-COF electron transfer by covalent coupling, resulting in electron accumulation in the cyano/pyridine moieties of the COF for CO2 reduction and holes in the semiconductor for H2 O oxidation, thus mimicking natural photosynthesis.Entities:
Keywords: CO2 photoreduction; Z-scheme; artificial photosynthesis; covalent organic frameworks; semiconductors
Year: 2020 PMID: 31989745 DOI: 10.1002/anie.202000929
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336