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Zeolitic-imidazole framework-8 (ZIF-8) membranes have shown exceptional propylene/propane separation performances. Their commercial applications have, however, been impeded by several challenges. One such challenge is the difficulty of managing microstructural defects ( i.e. , grain boundary defects) in a consistent manner, leading to poor membrane performances and ultimately to a reproducibility issue. Herein, we introduce a new effective strategy to seal the microstructural defects of polycrystalline ZIF-8 membranes using post-synthetic surface polymerization which consists of two steps: (1) introduction of initiator ligands on the membrane surface by post-synthetic ligand exchange and (2) in situ polymerization of poly(methyl methacrylate) (PMMA) via atom transfer radical polymerization. The ZIF-8 membranes were fully covered with ultra-thin PMMA layers of sub-10 nm thickness, increasing the propylene/propane separation factor from ∼60 to ∼106 with unexpectedly increased propylene permeance, effectively improving the membrane reproducibility. The enhanced separation properties of the PMMA-coated ZIF-8 membranes were attributed to the ultra-thin PMMA layers as well as to the possible facilitated propylene transport by Cu ions in the PMMA layers.
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All-dry free radical polymerization inside nanopores: Ion-milling-enabled coating thickness profiling revealed “necking” phenomena
Conformal coating of nanopores with functional polymer nanolayers is the key to many emerging technologies such as miniature sensors and membranes for advanced molecular separations. While the polymer coatings are often used to introduce functional moieties, their controlled growth under nanoconfinement could serve as a new approach to manipulate the size and shape of coated nanopores, hence, enabling novel functions like molecular separation. However, precise control of coating thickness in the longitudinal direction of a nanopore is limited by the lack of a characterization method to profile coating thickness within the nanoconfined space. Here, we report an experimental approach that combines ion milling (IM) and high-resolution field emission scanning electron microscopy (FESEM) for acquiring an accurate depth profile of ultrathin (∼20 nm or less) coatings synthesized inside nanopores via initiated chemical vapor deposition (iCVD). The enhanced capability of this approach stems from the excellent x–y resolution achieved by FESEM (i.e., 4.9 nm/pixel), robust depth ( z) control enabled by IM (step size as small as 100 nm with R2 = 0.992), and the statistical power afforded by high-throughput sampling (i.e., ∼2000 individual pores). With that capability, we were able to determine with unparalleled accuracy and precision the depth profile of coating thickness and iCVD kinetics along 110-nm-diameter nanopores. That allowed us to uncover an unexpected coating depth profile featuring a maximum rate of polymerization at ∼250 nm underneath the top surface, i.e., down the pores, which we termed “necking.” The necking phenomenon deviates considerably from the conventionally assumed monotonous decrease in thickness along the longitudinal direction into a nanopore, as predicted by the diffusion-limited kinetics model of free radical polymerization. An initiator-centric collision model was then developed, which suggests that under the experimental conditions, the confinement imposed by the nanopores may lead to local amplification of the effective free radical concentration at z ≤ 100 nm and attenuation at z ≥ 500 nm, thus contributing to the observed necking phenomenon. The ion-milling-enabled depth profiling of ultrathin coatings inside nanopores, along with the initiator-mediated coating thickness control in the z-direction, may serve to enhance the performance of size-exclusion filtration membranes and even provide more flexible control of nanopore shape in the z dimension.
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- PAR ID:
- 10365007
- Publisher / Repository:
- American Vacuum Society
- Date Published:
- Journal Name:
- Journal of Vacuum Science & Technology A
- Volume:
- 40
- Issue:
- 3
- ISSN:
- 0734-2101
- Page Range / eLocation ID:
- Article No. 033406
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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