Covalent Organic Frameworks for Water Sorption: The Importance of Framework Physical Stability

21 March 2025, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Covalent organic frameworks (COFs) have garnered growing interest as water-sorption adsorbents. While the chemical stability of most COFs in liquid-phase water is well-established, there are limited studies on their framework physical stability in water vapor. This refers to maintaining the ordered structure of COFs without disrupting their chemical bonds, a factor that significantly influences water sorption. Here, we examined the water-vapor stability of three distinct two-dimensional COFs with various pore sizes. Microporous COFs exhibited superior stability than mesoporous COFs, albeit with reduced water-uptake capacity. Mesoporous keto-enamine-linked COFs with the intralayer hydrogen bonds between carbonyl oxygen and secondary amine hydrogen atoms exhibited markedly improved water-vapor stability compared to imine-linked COFs, which was further confirmed by molecular dynamics simulations, density functional theory calculations, and the extended water adsorption-desorption cycling test (200 cycles). Finally, a COF-coated heat exchanger was fabricated to demonstrate air dehumidification at a device level.

Keywords

Covalent organic frameworks
water sorption
framework physical stability
air dehumidification

Supplementary materials

Title
Description
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Supporting information
Description
Supporting information for the main manuscript.
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Title
Zhao_2025_COFs for water_SV 1
Description
MD of TFB-BD COF
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Zhao_2025_COFs for water_SV 2
Description
MD of TpOMe-BD COF
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Zhao_2025_COFs for water_SV 3
Description
MD of TpOMe-BpyD COF
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