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With increasing demands for high-performance water sorption materials, metal-organic frameworks (MOFs) have gained considerable attention due to their high maximum uptake capacities. In many cases, however, high overall capacity is not necessarily accomplishing high working capacity under operating conditions, due to insufficient hydrophilicity and/or water stability. Herein, we present a post-synthetic modification (PSM) of MOF-808, with di-sulfonic acids enhancing simultaneously its hydrophilicity and water stability without sacrificing its uptake capacity of ≈30 mmol g . Di-sulfonic acid PSM enabled a shift of the relative humidity (RH) associated with a sharp step in water vapor sorption from 35-40 % RH in MOF-808 to below 25 % RH. While MOF-808 lost uptake capacity and crystallinity over multiple sorption/desorption cycles, the di-sulfonic acid PSM MOF-808 retained >80 % of the original capacity. PSM MOF-808 exhibited good hydrothermal stability up to 60 °C and high swing capacity.
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http://dx.doi.org/10.1002/anie.202209034 | DOI Listing |
ACS Appl Mater Interfaces
March 2025
Institute of Functional Materials and Catalysis, Faculty of Chemistry, University of Vienna, Währinger Str. 42, 1090 Vienna, Austria.
Metal-organic frameworks (MOFs) show promising results in various fields, such as gas separation and catalysis, but they face limitations due to problems associated with their low processability. This study addresses these challenges by utilizing postsynthetic modification (PSM) of NH-UiO-66 and NH-MOF-808 with 1,3,5-benzene tricarbaldehyde (BTCA) to form hybrid aerogels consisting of MOF-loaded covalent organic framework (COF). BTCA-modified MOF nanoparticles via imine bond formation were confirmed by H NMR, FTIR, and solid-state C NMR spectroscopies.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
Key Laboratory of Green and Precise Synthetic Chemistry and Applications, Ministry of Education, School of Chemistry and Material Science, Huaibei Normal University, Huaibei 235000, China. Electronic address:
To enhance the economic viability of photocatalytic materials for carbon capture and conversion, the challenge of employing expensive photosensitizer must be overcome. This study aims to improve the visible light utilization with zirconium-based metal-organic frameworks (Zr-MOFs) by employing a multi-component post-synthetic modification (PSM) strategy. An economical photosensitiser and copper ions are introduced into MOF 808 to enhance its photoreduction properties.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2022
Department of Chemical and Biomolecular Engineering & Institute for NanoBioTechnology, Johns Hopkins University, 3400N. Charles Street, Baltimore, MD 21218, USA.
With increasing demands for high-performance water sorption materials, metal-organic frameworks (MOFs) have gained considerable attention due to their high maximum uptake capacities. In many cases, however, high overall capacity is not necessarily accomplishing high working capacity under operating conditions, due to insufficient hydrophilicity and/or water stability. Herein, we present a post-synthetic modification (PSM) of MOF-808, with di-sulfonic acids enhancing simultaneously its hydrophilicity and water stability without sacrificing its uptake capacity of ≈30 mmol g .
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
April 2021
College of Chemistry, Liaoning University, 66 Chongshan Middle Road, Shenyang, Liaoning 110036, People's Republic of China. Electronic address:
Dyes detection remains a serious task because of their high toxicity. In present work, designed Eu functionalized Zr-metal-organic framework (Eu@Zr-MOF-808) as fluorescent probe was constructed via post-synthetic modification (PSM) for rapid monitoring four most commonly used dyes (malachite green (MG), brilliant green (BG), alizarin red S (ARS), indigo red (IDR)). Systematic exploring on the sensing mechanism reveals that fluorescence resonance energy transfer (FRET) for BG, MG and IDR and inner filter effect (IFE) for ARS contribute to the realization of the fluorescence quenching process.
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