Fabrication of 2D Metal–Organic Framework Nanosheets with Highly Colloidal Stability and High Yield through Coordination Modulation
2D metal–organic frameworks (MOFs) are promising 2D materials with a wide range of applications due to their unique physical and chemical properties. However, 2D MOFs are prone to stacking due to their ultrathin thickness, and the high-yield preparation method of 2D MOFs is highly demanded. In this...
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Published in | ACS applied materials & interfaces Vol. 13; no. 33; pp. 39755 - 39762 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
American Chemical Society
25.08.2021
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Subjects | |
Online Access | Get full text |
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Summary: | 2D metal–organic frameworks (MOFs) are promising 2D materials with a wide range of applications due to their unique physical and chemical properties. However, 2D MOFs are prone to stacking due to their ultrathin thickness, and the high-yield preparation method of 2D MOFs is highly demanded. In this work, a rapid and scalable method is novelistically presented to prepare 2D MOFs with highly colloidal stability and high yield through coordination modulation at room temperature. A well-ordered CuBDC-MBA nanosheet (BDC, 1,4-benzenedicarboxylic; MBA, 4-methoxybenzoic acid) fabricated by introducing MBA as a modulator exhibits extremely stable colloid suspension for 6 months and the yield of well-dispersed CuBDC-MBA is higher than 88.6%. As MBA successfully participates in synthetic coordination of CuBDC-MBA and is presumably installed on the edge of 2D MOFs with low MBA content due to anisotropic growth, CuBDC-MBA and CuBDC are similar with respect to nanosheet morphology, integrated crystal structure, and porosity. Moreover, well-dispersed CuBDC-MBA shows higher catalytic effectiveness for the cycloaddition reaction of CO2 with 1.5 times higher yield than CuBDC. Thus, this method can provide a new idea based on coordination modulation to directly fabricate 2D MOFs with purposeful properties. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1944-8244 1944-8252 1944-8252 |
DOI: | 10.1021/acsami.1c11373 |