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用于金属有机框架可扩展单晶外延的主客体电荷转移

Host-guest charge transfer for scalable single crystal epitaxy of a metal-organic framework.

作者信息

Mantel Arthur, Stöger Berthold, Prado-Roller Alexander, Shiozawa Hidetsugu

机构信息

J. Heyrovsky Institute of Physical Chemistry, Czech Academy of Sciences, Prague, Czechia.

X-ray Centre, TU Wien, Vienna, Austria.

出版信息

Commun Mater. 2024;5(1):220. doi: 10.1038/s43246-024-00657-3. Epub 2024 Oct 9.

Abstract

Methods to grow large crystals provide the foundation for material science and technology. Here we demonstrate single crystal homoepitaxy of a metal-organic framework (MOF) built of zinc, acetate and terephthalate ions, that encapsulate arrays of octahedral zinc dimethyl sulfoxide (DMSO) complex cations within its one-dimensional (1D) channels. The three-dimensional framework is built of two-dimensional Zn-terephthalate square lattices interconnected by anionic acetate pillars through diatomic zinc nodes. The charge of the anionic framework is neutralized by the 1D arrays of cations that fill every second 1D channel of the framework. It is demonstrated that the repeatable and scalable epitaxy allows square cuboids of this charge-transfer MOF to grow stepwise to sizes in the centimeter range. The continuous growth with no size limits can be attributed to the ionic nature of the anionic framework with cationic 1D molecular fillers. These findings pave the way for epitaxial growth of bulk crystals of MOFs.

摘要

生长大晶体的方法为材料科学与技术奠定了基础。在此,我们展示了一种由锌、乙酸根和对苯二甲酸根离子构建的金属有机框架(MOF)的单晶同质外延,该框架在其一维(1D)通道内封装了八面体锌二甲基亚砜(DMSO)络合阳离子阵列。三维框架由二维Zn - 对苯二甲酸方形晶格构成,通过阴离子乙酸根支柱经双原子锌节点相互连接。阴离子框架的电荷由填充框架每隔一个1D通道的阳离子1D阵列中和。结果表明,这种可重复且可扩展的外延使得这种电荷转移MOF的方形长方体能够逐步生长到厘米级尺寸。无尺寸限制的连续生长可归因于具有阳离子1D分子填料的阴离子框架的离子性质。这些发现为MOF块状晶体的外延生长铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78da/11488492/cecd7bb8a195/43246_2024_657_Figa_HTML.jpg

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