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Article: Low-dimensional assemblies of metal-organic framework particles and mutually coordinated anisotropy

TitleLow-dimensional assemblies of metal-organic framework particles and mutually coordinated anisotropy
Authors
Issue Date9-Jul-2022
PublisherNature Research
Citation
Nature Communications, 2022, v. 13, n. 1 How to Cite?
Abstract

Colloidal self-assembly is a powerful strategy for designing materials, and MOFs offer wide structural and functional diversity. Here, authors present the self-assembly of MOF microcrystals using depletion interactions to form low-dimensional MOF colloidal superstructures with anisotropic properties.Assembling metal-organic framework (MOF)-based particles is an emerging approach for creating colloidal superstructures and hierarchical functional materials. However, realization of this goal requires strategies that not only regulate particle interactions but also harness the anisotropic morphologies and functions of various frameworks. Here, by exploiting depletion interaction induced by ionic amphiphiles, we show the assembly of a broad range of low-dimensional MOF colloidal superstructures, including 1D straight chains, alternating or bundled chains, 2D films of hexagonal, square, centered rectangular, and snowflake-like architectures, and quasi-3D supercrystals. With well-defined polyhedral shapes, the MOF particles are mutually oriented upon assembly, producing super-frameworks with hierarchically coordinated crystallinity and micropores. We demonstrate this advantage by creating functional MOF films with optical anisotropy, in our cases, birefringence and anisotropic fluorescence. Given the variety of MOFs available, our technique should allow access to advanced materials for sensing, optics, and photonics.


Persistent Identifierhttp://hdl.handle.net/10722/337901
ISSN
2023 Impact Factor: 14.7
2023 SCImago Journal Rankings: 4.887
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLyu, DP-
dc.contributor.authorXu, W-
dc.contributor.authorPayong, JEL-
dc.contributor.authorZhang, TR-
dc.contributor.authorWang, YF-
dc.date.accessioned2024-03-11T10:24:46Z-
dc.date.available2024-03-11T10:24:46Z-
dc.date.issued2022-07-09-
dc.identifier.citationNature Communications, 2022, v. 13, n. 1-
dc.identifier.issn2041-1723-
dc.identifier.urihttp://hdl.handle.net/10722/337901-
dc.description.abstract<p>Colloidal self-assembly is a powerful strategy for designing materials, and MOFs offer wide structural and functional diversity. Here, authors present the self-assembly of MOF microcrystals using depletion interactions to form low-dimensional MOF colloidal superstructures with anisotropic properties.Assembling metal-organic framework (MOF)-based particles is an emerging approach for creating colloidal superstructures and hierarchical functional materials. However, realization of this goal requires strategies that not only regulate particle interactions but also harness the anisotropic morphologies and functions of various frameworks. Here, by exploiting depletion interaction induced by ionic amphiphiles, we show the assembly of a broad range of low-dimensional MOF colloidal superstructures, including 1D straight chains, alternating or bundled chains, 2D films of hexagonal, square, centered rectangular, and snowflake-like architectures, and quasi-3D supercrystals. With well-defined polyhedral shapes, the MOF particles are mutually oriented upon assembly, producing super-frameworks with hierarchically coordinated crystallinity and micropores. We demonstrate this advantage by creating functional MOF films with optical anisotropy, in our cases, birefringence and anisotropic fluorescence. Given the variety of MOFs available, our technique should allow access to advanced materials for sensing, optics, and photonics.</p>-
dc.languageeng-
dc.publisherNature Research-
dc.relation.ispartofNature Communications-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleLow-dimensional assemblies of metal-organic framework particles and mutually coordinated anisotropy-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1038/s41467-022-31651-3-
dc.identifier.pmid35810163-
dc.identifier.scopuseid_2-s2.0-85133650926-
dc.identifier.volume13-
dc.identifier.issue1-
dc.identifier.eissn2041-1723-
dc.identifier.isiWOS:000822541400002-
dc.publisher.placeBERLIN-
dc.identifier.issnl2041-1723-

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