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用于具有精确可控介孔/微孔纳米域的碗状金属有机框架纳米反应器的各向异性界面连续组装

Anisotropic Interface Successive Assembly for Bowl-Shaped Metal-Organic Framework Nanoreactors with Precisely Controllable Meso-/Microporous Nanodomains.

作者信息

Zhong Guiyuan, Chen Guangrui, Han Ji, Sun Ruigang, Zhao Bin, Xu Haidong, Wang Sibo, Yamauchi Yusuke, Guan Buyuan

机构信息

State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, Changchun 130012, P. R. China.

State Key Laboratory of Photocatalysis on Energy and Environment, College of Chemistry, Fuzhou University, Fuzhou, Fujian 350116, P. R. China.

出版信息

ACS Nano. 2023 Dec 26;17(24):25061-25069. doi: 10.1021/acsnano.3c07635. Epub 2023 Dec 12.

Abstract

Colloidal metal-organic framework (MOF) nanoparticles, with tailored asymmetric nanoarchitectures and hierarchical meso-/microporosities, have significant implications in high-performance nanocatalysts, nanoencapsulation carriers, and intricate assembly architectures. However, the methodology that could achieve precise control over the anisotropic growth of asymmetric MOF particles with tailored distributions of meso- and microporous regions has not yet been established. In this study, we introduce a facile anisotropic interface successive assembly approach to synthesize asymmetric core-shell MOF (ZIF-67) nanobowls with worm-like mesopores in the core and intrinsic micropores in the shell. Our synthesis pathway relies on anisotropic nucleation of mesoporous MOF nanohemispheres on emulsion interfaces through the cooperative assembly of surfactants and MOF precursors. This is followed by the growth of microporous MOF layers on both interfaces of mesoporous cores and emulsion droplets, resulting in a hierarchically porous core-shell nanostructure. By utilizing this multi-interface-driven approach, we enable the creation of diverse geometries and distributions of mesopores and micropores in asymmetric MOF nanoarchitectures. The obtained bowl-like meso-/microporous core-shell ZIF-67 particles exhibit enhanced catalytic activity for CO cycloaddition, attributed to reactant accumulation within the bowl-like architecture, active site accessibility in the open mesoporous core, and improved structural stability. Overall, our study provides insights and inspiration for exploring the intricate asymmetric nanostructures of hierarchically porous MOFs with diverse potential applications.

摘要

具有定制的不对称纳米结构和分级介孔/微孔的胶体金属有机框架(MOF)纳米颗粒在高性能纳米催化剂、纳米封装载体和复杂组装结构方面具有重要意义。然而,尚未建立能够精确控制具有定制介孔和微孔区域分布的不对称MOF颗粒各向异性生长的方法。在本研究中,我们引入了一种简便的各向异性界面连续组装方法,以合成具有核内蠕虫状介孔和壳内固有微孔的不对称核壳MOF(ZIF-67)纳米碗。我们的合成途径依赖于通过表面活性剂和MOF前体的协同组装,在乳液界面上介孔MOF纳米半球的各向异性成核。随后在介孔核和乳液滴的两个界面上生长微孔MOF层,从而形成分级多孔核壳纳米结构。通过利用这种多界面驱动方法,我们能够在不对称MOF纳米结构中创建介孔和微孔的多种几何形状和分布。所获得的碗状介孔/微孔核壳ZIF-67颗粒对CO环加成反应表现出增强的催化活性,这归因于反应物在碗状结构内的积累、开放介孔核中活性位点的可及性以及结构稳定性的提高。总体而言,我们的研究为探索具有多种潜在应用的分级多孔MOF复杂不对称纳米结构提供了见解和灵感。

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