Mechanochemistry-driven phase transformation of crystalline covalent triazine frameworks assisted by alkaline molten salts

被引:9
|
作者
Fan, Juntian [1 ]
Suo, Xian [1 ]
Wang, Tao [2 ]
Wang, Zongyu [2 ]
Do-Thanh, Chi-Linh [1 ]
Mahurin, Shannon M. [2 ]
Kobayashi, Takeshi [3 ]
Yang, Zhenzhen [2 ]
Dai, Sheng [1 ,2 ]
机构
[1] Univ Tennessee, Inst Adv Mat & Mfg, Dept Chem, Knoxville, TN 37996 USA
[2] Oak Ridge Natl Lab, Chem Sci Div, Oak Ridge, TN 37831 USA
[3] Iowa State Univ, US DoE Ames Lab, Ames, IA 50011 USA
关键词
ORGANIC FRAMEWORKS; CO2; POLYMERS; TEMPERATURE; MEMBRANES; CAPTURE; DESIGN;
D O I
10.1039/d2ta02117j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Covalent triazine frameworks (CTFs) have shown wide applications in the fields of separation, catalysis, energy storage, and beyond. However, it is a long-term challenging subject to fabricate high-quality CTF materials via facile procedures. Herein, a mechanochemistry-driven procedure was developed to achieve phase transformation of crystalline CTFs assisted by alkaline molten salts. The transformation of CTF-1 from staggered AB to eclipsed AA stacking mode was achieved by short time (30 min) mechanochemical treatment in the presence of molten salts composed of LiOH/KOH, generating high-quality CTF-1 material with high crystallinity, high surface area (625 m(2) g(-1)), and permanent/ordered porosity without carbonization under ambient conditions. This facile procedure could be extended to provide nanoporous three-dimensional CTF materials.
引用
收藏
页码:14310 / 14315
页数:6
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