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Ozonolysis–oxidation-driven top-down strategy for the target preparation of ultrathin 2D metal–organic framework monolayersElectronic supplementary information (ESI) available. See DOI: https://doi.org/10.1039/d3im00045a

Authors :
Zhuo, Baoliu
Tan, Aidong
Xiang, Zhipeng
Piao, Jinhua
Zheng, Wenhao
Wan, Kai
Liang, Zhenxing
Fu, Zhiyong
Source :
Industrial Chemistry & Materials; 2024, Vol. 2 Issue: 1 p110-117, 8p
Publication Year :
2024

Abstract

Two-dimensional metal–organic-framework (2D MOF) nanosheets with a modular nature and tunable structures exhibit a bright future for sensors, separation, and catalysis. Developing ultrathin 2D MOF nanosheets with unique physical and chemical properties is urgently required but very challenging. Although the chemical exfoliation strategy has been regarded as a promising way to exfoliate large amounts of three-dimensional (3D) pillar-layered MOFs, this method still faces many problems and remains insufficient. In this study, a novel chemical exfoliation method is developed for the target preparation of 2D MOF monolayers from the 3D pillar-layered MOFs. The Co/Zn/Cu-MOFs with a pillar ligand of trans-1,2-bis(4-pyridyl)ethylene (bipyen) are subjected to be broken by the cleavage of CC bonds in the bipyen ligands viaan ozone oxidation reaction. As chemical exfoliation is processed viathe oxidation of the pillar ligand by ozone, the thickness of the 2D MOFs can be tuned by the control of oxidation time and the obtained 2D Co/Zn/Cu-MOF monolayers are functionalized with a –COOH group. This study provides an effective and general chemical exfoliation method to prepare monolayer MOFs from the 3D pillar-layered MOFs with bipyen as the pillar ligand.Keywords: 3D pillar-layered MOFs; Ultrathin 2D MOF monolayers; Top-down strategy; Chemical exfoliation; Ozonolysis–oxidation.

Details

Language :
English
ISSN :
27552608 and 27552500
Volume :
2
Issue :
1
Database :
Supplemental Index
Journal :
Industrial Chemistry & Materials
Publication Type :
Periodical
Accession number :
ejs65589256
Full Text :
https://doi.org/10.1039/d3im00045a