Acoustomicrofluidic Defect Engineering and Ligand Exchange in ZIF‐8 Metal–Organic Frameworks

Author:

Massahud Emily1,Ahmed Heba1,Babarao Ravichandar23,Ehrnst Yemima1,Alijani Hossein1,Darmanin Connie45,Murdoch Billy J.6,Rezk Amgad R.1,Yeo Leslie Y.1ORCID

Affiliation:

1. Micro/Nanophysics Research Laboratory RMIT University Melbourne VIC 3000 Australia

2. Manufacturing Business Unit Commonwealth Scientific and Industrial Research Organization (CSIRO) Manufacturing Clayton VIC 3168 Australia

3. Centre for Advanced Materials and Industrial Chemistry, School of Science RMIT University Melbourne VIC 3000 Australia

4. Department of Mathematical and Physical Sciences School of Engineering Computing and Mathematical Sciences La Trobe University Melbourne VIC 3086 Australia

5. La Trobe Institute for Molecular Science La Trobe University Melbourne VIC 3086 Australia

6. RMIT Microscopy and Microanalysis Facility STEM College RMIT University Melbourne VIC 3000 Australia

Abstract

AbstractA way through which the properties of metal–organic frameworks (MOFs) can be tuned is by engineering defects into the crystal structure. Given its intrinsic stability and rigidity, however, it is difficult to introduce defects into zeolitic imidazolate frameworks (ZIFs)—and ZIF‐8, in particular—without compromising crystal integrity. In this work, it is shown that the acoustic radiation pressure as well as the hydrodynamic stresses arising from the oscillatory flow generated by coupling high frequency (MHz‐order) hybrid surface and bulk acoustic waves into a suspension of ZIF‐8 crystals in a liquid pressure transmitting medium is capable of driving permanent structural changes in their crystal lattice structure. Over time, the enhancement in the diffusive transport of guest molecules into the material's pores as a consequence is shown to lead to expansion of the pore framework, and subsequently, the creation of dangling‐linker and missing‐linker defects, therefore offering the possibility of tuning the type and extent of defects engineered into the MOF through the acoustic exposure time. Additionally, the practical utility of the technology is demonstrated for one‐pot, simultaneous solvent‐assisted ligand exchange under ambient conditions, for sub‐micron‐dimension ZIF‐8 crystals and relatively large ligands—more specifically 2‐aminobenzimidazole—without compromising the framework porosity or overall crystal structure.

Funder

Australian Research Council

Publisher

Wiley

Subject

General Materials Science,General Chemistry

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