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  4. Fine-tuning ultramicroporosity in PIM-1 membranes by aldehyde functionalization for efficient hydrogen separation

Fine-tuning ultramicroporosity in PIM-1 membranes by aldehyde functionalization for efficient hydrogen separation

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2024_TL_PIMCHO_JMCA (1).pdf

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Author(s)
Lee, Tae Hoon
•
Joo, Taigyu
•
Jean-Baptiste, Philippe
•
Dean, Pablo A
•
Yeo, Jing Ying
•
Smith, Zachary P
Date Issued
August 19, 2024
Journal
Journal of Materials Chemistry A
Publisher
Royal Society of Chemistry
Citation
Tae Hoon Lee, Taigyu Joo, Philippe Jean-Baptiste, Pablo A. Dean, Jing Ying Yeo, Zachary P. Smith; Fine-tuning ultramicroporosity in PIM-1 membranes by aldehyde functionalization for efficient hydrogen separation. J. Mater. Chem. A 2024; 12 (36): 24519–24529.
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Author's final manuscript
Abstract
Polymers of intrinsic microporosity (PIMs) have shown great potential for membrane-based hydrogen separations. The archetypal PIM, PIM-1, features hydrogen permeability that is 2–3 orders of magnitude higher than that of conventional polymers. However, the hydrogen selectivities of PIM-1 still need to be improved to meet the purity required for hydrogen production and distribution processes. Herein, we report a facile approach to fine-tune the microstructure of PIM-1 films by converting the nitrile groups of PIM-1 into aldehyde groups at room temperature. The aldehyde-functionalized PIM-1 (PIM-CHO) has a significantly higher concentration of ultramicropores (<7 Å) compared to PIM-1 as confirmed by gas sorption and X-ray scattering analyses. Ultimately, this feature results in excellent H2/N2 and H2/CH4 separation performance for PIM-CHO, approaching the most recent 2015 upper bound and outperforming all post-synthetically modified PIM-1 membranes reported to date. Mixed-gas transport studies also demonstrate the excellent potential of PIM-CHO for its deployment in practical applications.
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Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
Persistent DSpace Link
https://dspace.mit.edu/handle/1721.1/169100
DOI of Published Version
https://doi.org/10.1039/d4ta04082a
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