| Literature DB >> 30920709 |
Manying Liu1, Kai Jiang2, Xing Ding2, Shaolei Wang1, Chengxin Zhang1, Jing Liu1, Zhen Zhan1, Guang Cheng1, Buyi Li3, Hao Chen2, Shangbin Jin1, Bien Tan1.
Abstract
The synthesis of highly crystalline covalent triazine frameworks (CTFs) with ultrastrong covalent bonds (aromatic CN) from the triazine linkage presents a great challenge to synthetic chemists. Herein, the synthesis of highly crystalline CTFs via directly controlling the monomer feeding rate is reported. By tuning the feeding rate of monomers, the crystallization process can be readily governed in a controlled manner in an open system. The sample of CTF-HUST-HC1 with abundant exposed {001} crystal facets has the better crystallinity and thus is selected to study the effect of high crystallinity on photoelectric properties. Owing to the better separation of photogenerated electron-hole pairs and charge transfer, the obtained highly ordered CTF-HUST-HC1 has superior performance in the photocatalytic removal of nitric oxide (NO) than its lesser crystalline counterparts and g-C3 N4 .Entities:
Keywords: controlling feeding rate; covalent organic frameworks; covalent triazine frameworks; high crystallinity; photocatalysis
Year: 2019 PMID: 30920709 DOI: 10.1002/adma.201807865
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849