| Literature DB >> 31930618 |
Siquan Zhang1, Guang Cheng1, Liping Guo1, Ning Wang1, Bien Tan1, Shangbin Jin1.
Abstract
Methods to synthesize crystalline covalent triazine frameworks (CTFs) are limited and little attention has been paid to development of hydrophilic CTFs and photocatalytic overall water splitting. A route to synthesize crystalline and hydrophilic CTF-HUST-A1 with a benzylamine-functionalized monomer is presented. The base reagent used plays an important role in the enhancement of crystallinity and hydrophilicity. CTF-HUST-A1 exhibits good crystallinity, excellent hydrophilicity, and excellent photocatalytic activity in sacrificial photocatalytic hydrogen evolution (hydrogen evolution rate up to 9200 μmol g-1 h-1 ). Photocatalytic overall water splitting is achieved by depositing dual co-catalysts in CTF-HUST-A1, with H2 evolution and O2 evolution rates of 25.4 μmol g-1 h-1 and 12.9 μmol g-1 h-1 in pure water without using sacrificial agent.Entities:
Keywords: benzylamine; covalent triazine frameworks; hydrophilicity; photocatalysis
Year: 2020 PMID: 31930618 DOI: 10.1002/anie.201914424
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336