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ZIF-8薄膜膜中的空间功能梯度。

Spatial functionality gradient in a ZIF-8 thin film membrane.

作者信息

Archana Yadav K M, Mishra Girish, Kundu Susmita, Ghosh Soumya, Haldar Ritesh

机构信息

Tata Institute of Fundamental Research Hyderabad Gopanpally 500046 Hyderabad India

出版信息

Chem Sci. 2025 Sep 3. doi: 10.1039/d5sc04618a.

DOI:10.1039/d5sc04618a
PMID:40951773
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12427888/
Abstract

Zeolitic imidazolate framework-8 (ZIF-8), constructed from Zn ions and 2-methylimidazole (mIm) linkers, is widely recognized for its excellent thermal and chemical stability, making it a strong candidate for chemical separation and heterogeneous catalysis. In this study, we report a new crystalline phase of functionalized ZIF-8 featuring a spatially graded distribution of chemical functionalities. This anisotropic functionalization is achieved a vapor-phase process applied to a ZIF-8 monolithic film. Anisotropic diffusion of a reactive linker-imidazole-2-carboxaldehyde (CHO-Im)-into the ZIF-8 monolith results in a gradient incorporation of CHO-Im, yielding a ZIF-8-CHO monolith. Spatial anisotropy of the CHO functional groups is confirmed through X-ray diffraction, scanning electron microscopy, and vibrational spectroscopy. To demonstrate its potential, we fabricated an anodic aluminium oxide-supported membrane and highlighted its enhanced gas permselectivity compared to pristine membranes.

摘要

由锌离子和2-甲基咪唑(mIm)连接体制成的沸石咪唑酯骨架-8(ZIF-8),因其出色的热稳定性和化学稳定性而广受认可,这使其成为化学分离和多相催化的有力候选材料。在本研究中,我们报告了一种功能化ZIF-8的新晶相,其具有化学官能团的空间梯度分布。这种各向异性功能化是通过将气相过程应用于ZIF-8整体膜来实现的。反应性连接体-咪唑-2-甲醛(CHO-Im)向ZIF-8整体的各向异性扩散导致CHO-Im的梯度掺入,从而产生ZIF-8-CHO整体。通过X射线衍射、扫描电子显微镜和振动光谱证实了CHO官能团的空间各向异性。为了证明其潜力,我们制备了一种阳极氧化铝支撑膜,并强调了其与原始膜相比增强的气体渗透选择性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db6/12427888/498c40ac1129/d5sc04618a-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db6/12427888/3dc7f5894e62/d5sc04618a-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db6/12427888/39ffe2a312f1/d5sc04618a-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db6/12427888/121180113166/d5sc04618a-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db6/12427888/bbdbdbf03ad9/d5sc04618a-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db6/12427888/28f5a1a22eca/d5sc04618a-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db6/12427888/498c40ac1129/d5sc04618a-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db6/12427888/3dc7f5894e62/d5sc04618a-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db6/12427888/39ffe2a312f1/d5sc04618a-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db6/12427888/121180113166/d5sc04618a-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db6/12427888/bbdbdbf03ad9/d5sc04618a-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db6/12427888/28f5a1a22eca/d5sc04618a-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7db6/12427888/498c40ac1129/d5sc04618a-f5.jpg

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本文引用的文献

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J Am Chem Soc. 2025 May 14;147(19):16481-16493. doi: 10.1021/jacs.5c02940. Epub 2025 May 5.
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Diffusion-programmed catalysis in nanoporous material.纳米多孔材料中的扩散程序催化
Nat Commun. 2025 Feb 3;16(1):1231. doi: 10.1038/s41467-025-56575-6.
3
Regulated Charge Transfer in Donor-Acceptor Metal-Organic Frameworks for Highly-Sensitive Photodetectors.
Angew Chem Int Ed Engl. 2024 Dec 20;63(52):e202414526. doi: 10.1002/anie.202414526. Epub 2024 Nov 26.
4
Steering diffusion selectivity of chemical isomers within aligned nanochannels of metal-organic framework thin film.在金属有机框架薄膜的排列纳米通道内控制化学异构体的扩散选择性。
Nat Commun. 2024 Nov 8;15(1):9636. doi: 10.1038/s41467-024-53207-3.
5
Anisotropic Porosity and Interface Synergy Enhanced Gas Permselectivity in Heterolayer Metal-Organic Framework Membrane.各向异性孔隙率和界面协同作用增强了异质层金属有机框架膜的气体渗透选择性
Chemistry. 2024 Dec 23;30(72):e202403607. doi: 10.1002/chem.202403607. Epub 2024 Nov 12.
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Multifunctional and Hierarchical Porous ZIF-8: Amine and Thiol Tagged via Mixed Multivariate Ligand Strategies for Enhanced CO and Iodine Adsorption.
ChemSusChem. 2025 Feb 16;18(4):e202401968. doi: 10.1002/cssc.202401968. Epub 2024 Nov 7.
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