硬 "乳液诱导界面超组装:二维分层多孔金属有机框架纳米结构的一般策略。

IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Ji Han, Haidong Xu, Bin Zhao, Ruigang Sun, Guangrui Chen, Tianyu Wu, Guiyuan Zhong, Yanjing Gao, Song Lin Zhang, Yusuke Yamauchi* and Buyuan Guan*, 
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引用次数: 0

摘要

具有可定制中孔/宏孔的二维(2D)分层多孔金属有机框架(MOF)纳米结构在增强传质动力学、增加可访问活性位点从而提高异相催化性能方面大有可为。然而,实现具有可控分层孔隙率和厚度的二维独立 MOF 纳米片的一般合成仍然是一项具有挑战性的任务。在此,我们提出了一种巧妙的 "硬 "乳液诱导界面超组装策略,用于制备具有高度可访问孔道、可调中孔/大孔尺寸和可调厚度的二维分层多孔 UiO-66-NH2 纳米片。该方法依赖于在适当的水包油乳液中将油滴模板的几何形状从传统的零维(0D)"软 "液球转变为低于油的熔点/冰点的二维 "硬 "固体薄片。随后,二维 "硬 "乳液表面的表面活性剂交换促进了作为结构单元的原位介观结构 MOF 纳米复合材料的异质成核和界面超组装,以松散堆积的方式产生具有多模态微孔/介孔/大孔系统的二维 MOF 纳米片。重要的是,通过改变金属氧簇和有机配体,这种策略还可扩展到制备其他二维分层多孔 MOF 纳米片。得益于快速的传质和高度易得的路易斯酸位点,制备出的二维分层多孔 UiO-66-NH2 纳米片在缩水甘油基-2-甲基苯基醚的 CO2 环加成反应中实现了约 96% 的惊人催化产率,远远超过了使用传统 UiO-66-NH2 微孔晶体实现的约 29% 的产率。这种 "硬 "乳液诱导的界面超组装策略为合理构建具有定制理化特性的二维纳米结构分层 MOFs 铺平了一条新路,可用于多种潜在应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

“Hard” Emulsion-Induced Interface Super-Assembly: A General Strategy for Two-Dimensional Hierarchically Porous Metal–Organic Framework Nanoarchitectures

“Hard” Emulsion-Induced Interface Super-Assembly: A General Strategy for Two-Dimensional Hierarchically Porous Metal–Organic Framework Nanoarchitectures

“Hard” Emulsion-Induced Interface Super-Assembly: A General Strategy for Two-Dimensional Hierarchically Porous Metal–Organic Framework Nanoarchitectures

Two-dimensional (2D) hierarchically porous metal–organic framework (MOF) nanoarchitectures with tailorable meso-/macropores hold great promise for enhancing mass transfer kinetics, augmenting accessible active sites, and thereby boosting performance in heterogeneous catalysis. However, achieving the general synthesis of 2D free-standing MOF nanosheets with controllable hierarchical porosity and thickness remains a challenging task. Herein, we present an ingenious “hard” emulsion-induced interface super-assembly strategy for preparing 2D hierarchically porous UiO-66-NH2 nanosheets with highly accessible pore channels, tunable meso-/macropore sizes, and adjustable thicknesses. The methodology relies on transforming the geometric shape of oil droplet templates within appropriate oil-in-water emulsions from conventional zero-dimensional (0D) “soft” liquid spheres to 2D “hard” solid sheets below the oil’s melting/freezing point. Subsequent surfactant exchange on the surface of 2D “hard” emulsions facilitates the heterogeneous nucleation and interfacial super-assembly of in situ formed mesostructured MOF nanocomposites, serving as structural units, in a loosely packed manner to produce 2D MOF nanosheets with multimodal micro/meso-/macroporous systems. Importantly, this strategy can be extended to prepare other 2D hierarchically porous MOF nanosheets by altering metal-oxo clusters and organic ligands. Benefiting from fast mass transfer and highly accessible Lewis acidic sites, the resultant 2D hierarchically porous UiO-66-NH2 nanosheets deliver a fabulous catalytic yield of approximately 96% on the CO2 cycloaddition of glycidyl-2-methylphenyl ether, far exceeding the yield of approximately 29% achieved using conventional UiO-66-NH2 microporous crystals. This “hard” emulsion-induced interface super-assembly strategy paves a new path toward the rational construction of elaborate 2D nanoarchitecture of hierarchical MOFs with tailored physicochemical properties for diverse potential applications.

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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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