TY - JOUR
T1 - Porous Functionalized Covalent-Triazine Frameworks for Enhanced Adsorption Toward Polysulfides in Li-S Batteries and Organic Dyes
AU - Liu, Qianhui
AU - Yang, Shuhao
AU - Repich, Hlib
AU - Zhai, Yixuan
AU - Xu, Xiaosa
AU - Liang, Yeru
AU - Li, Hejun
AU - Wang, Hongqiang
AU - Xu, Fei
N1 - Publisher Copyright:
© Copyright © 2020 Liu, Yang, Repich, Zhai, Xu, Liang, Li, Wang and Xu.
PY - 2020/12/2
Y1 - 2020/12/2
N2 - The incorporation of functional building blocks to construct functionalized and highly porous covalent triazine frameworks (CTFs) is essential to the emerging adsorptive-involved field. Herein, a series of amide functionalized CTFs (CTF-PO71) have been synthesized using a bottom-up strategy in which pigment PO71 with an amide group is employed as a monomer under ionothermal conditions with ZnCl2 as the solvent and catalyst. The pore structure can be controlled by the amount of ZnCl2 to monomer ratio. Benefitting from the highly porous structure and amide functionalities, CTF-PO71, as a sulfur cathode host, simultaneously demonstrates physical confinement and chemical anchoring of sulfur species, thus leading to superior capacity, cycling stability, and rate capability in comparison to unfunctionalized CTF. Meanwhile, as an adsorbent of organic dye molecules, CTF-PO71 was demonstrated to exhibit strong chemical interactions with dye molecules, facilitating adsorption kinetics and thereby promoting the adsorption rate and capacity. Furthermore, the dynamic adsorption experiments of organic dyes from solutions showed selectivity/priority of CTF-PO71s for specific dye molecules.
AB - The incorporation of functional building blocks to construct functionalized and highly porous covalent triazine frameworks (CTFs) is essential to the emerging adsorptive-involved field. Herein, a series of amide functionalized CTFs (CTF-PO71) have been synthesized using a bottom-up strategy in which pigment PO71 with an amide group is employed as a monomer under ionothermal conditions with ZnCl2 as the solvent and catalyst. The pore structure can be controlled by the amount of ZnCl2 to monomer ratio. Benefitting from the highly porous structure and amide functionalities, CTF-PO71, as a sulfur cathode host, simultaneously demonstrates physical confinement and chemical anchoring of sulfur species, thus leading to superior capacity, cycling stability, and rate capability in comparison to unfunctionalized CTF. Meanwhile, as an adsorbent of organic dye molecules, CTF-PO71 was demonstrated to exhibit strong chemical interactions with dye molecules, facilitating adsorption kinetics and thereby promoting the adsorption rate and capacity. Furthermore, the dynamic adsorption experiments of organic dyes from solutions showed selectivity/priority of CTF-PO71s for specific dye molecules.
KW - covalent triazine-based frameworks
KW - functionalization
KW - lithium- sulfur batteries
KW - organic dye adsorption
KW - pore structure
UR - http://www.scopus.com/inward/record.url?scp=85097663681&partnerID=8YFLogxK
U2 - 10.3389/fchem.2020.584204
DO - 10.3389/fchem.2020.584204
M3 - 文章
AN - SCOPUS:85097663681
SN - 2296-2646
VL - 8
JO - Frontiers in Chemistry
JF - Frontiers in Chemistry
M1 - 584204
ER -