文献类型：期刊文献

英文题名：Design and syntheses of MOF/COF hybrid materials via postsynthetic covalent modification: An efficient strategy to boost the visible-light-driven photocatalytic performance

作者：Li, Fei[1];Wang, Dengke[1];Xing, Qiu-Ju[1];Zhou, Gang[1];Liu, Shan-Shan[1];Li, Yan[2];Zheng, Ling-Ling[1];Ye, Peng[1];Zou, Jian-Ping[1]

机构：[1]Nanchang Hangkong Univ, Key Lab Jiangxi Prov Persistent Pollutants Contro, Nanchang 330063, Jiangxi, Peoples R China;[2]East China Univ Sci & Technol, Sch Chem & Mol Engn, Shanghai 200237, Peoples R China

年份：2019

卷号：243

起止页码：621

外文期刊名：APPLIED CATALYSIS B-ENVIRONMENTAL

收录：;EI(收录号：20184606083194);WOS:【SCI-EXPANDED(收录号:WOS:000453616800064)】；

基金：We gratefully acknowledge the financial support of the NSF of China (51622806, 51878325, 51868050, 51378246 and 51720105001), the NSF of Jiangxi Province (20162BCB22017, 20165BCB18008, 20171ACB20017, and 20171BAB206049) and the graduate student innovation fund of Jiangxi province (YC2017012).

语种：英文

外文关键词：Covalent organic frameworks; Hydrogen evolution; Metal-organic frameworks; MOF/COF hybrid material; Photocatalysis

摘要：The search of novel visible-light-responsive porous materials is important because they hold great promise for applications in various fields. Herein, we report a novel strategy based on postsynthetic covalent modification for fabrication of hierarchical porous metal-organic frameworks/covalent organic frameworks (MOF/COF) hybrid materials. For the first time, benzoic acid-modified covalent triazine-based frameworks (B-CTF-1) are covalently bonded with MOFs (NH2-MIL-125(Ti) or NH2-UiO-66(Zr)) by using this strategy. Photocatalytic results show that the hydrogen production rate over 15 wt% NH2-MIL-125(Ti)/B-CTF-1 (15TBC) is 360 mu mol.h(-1).g(-1) under visible light irradiation, which is more than twice as much as that of the B-CTF-1. Meanwhile, the hybrid materials show higher stability as compared to the simple heterostructures of MOFs and COFs connected via Van der Waals force. Photoelectrochemical analyses and controlled experiments indicate that the superior photocatalytic performance of the MOF/COF hybrids can be attributed to the formation of amide bonds between B-CTF-1 and MOFs, which facilitate the charge separation efficiency and improve the stability of the photocatalyst. Finally, a possible mechanism to well explain the improved photocatalytic performance of the photocatalytic system was proposed. The present work provides a new idea to construct highly efficient and stable MOF/COF hybrid systems and broaden the applications of COF-based materials.