Abstract
Metal–organic frameworks (MOFs) are some of the best materials for energy-efficient separations, like membranes and adsorption processes, due to their nanoporosity and tunability. To tune a MOF for optimum separation of molecules with sub-angstrom differences in size, which is a common challenge in industrial separations, precise control of the local pore environment is required. Here, we explore the concept of “3-dimensional” linkers, i.e., linkers that contain sterically bulky non-planar cores, as a means to attain sub-angstrom control over MOF pore size and to control structural flexibility. In particular, the introduction of 3-dimensional linkers (3DLs) is shown to hinder global breathing transitions in MOFs. Because these linkers occupy a consistent volume regardless of their orientation, they also allow for precise size-based separation of very similar molecules, such as hexane isomers. Furthermore, we discuss the thermal stability of a subset of these materials, characterized through variable temperature X-ray diffraction and porosity measurements.
Original language | English (US) |
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Pages (from-to) | 1047-1056 |
Number of pages | 10 |
Journal | Journal of Materials Research |
Volume | 39 |
Issue number | 7 |
DOIs | |
State | Published - Apr 14 2024 |
Funding
O.K.F. and R.Q.S. gratefully acknowledge support from the Separation Science program of the U.S. Department of Energy (DE-FG02-08ER15967). C.S.S. thanks the International Institute of Nanotechnology at Northwestern University for support under the Ryan Fellowship.
Keywords
- Adsorption
- Metal–organic framework (MOF)
- Nanoscale
- x-ray diffraction (XRD)
ASJC Scopus subject areas
- General Materials Science
- Condensed Matter Physics
- Mechanics of Materials
- Mechanical Engineering