Time-efficient atmospheric water harvesting using Fluorophenyl oligomer incorporated MOFs.

Nat Commun

Department of Applied Chemistry, Center for Bionano Intelligence Education and Research, Hanyang University, ERICA, Ansan, 15588, Republic of Korea.

Published: November 2024

AI Article Synopsis

  • Adsorption-based atmospheric water harvesting (AWH) offers a potential solution for water scarcity in dry regions, but challenges remain in developing efficient adsorbents for low humidity conditions.
  • The study presents a new metal-organic framework (MOF) called FO@HK, which incorporates fluorophenyl oligomers to enhance water capture and allow easy release through sunlight.
  • FO@HK outperforms existing sorbents, achieving significant water harvest rates in outdoor tests, illustrating a promising approach to improve water collection technologies.

Article Abstract

Adsorption-based atmospheric water harvesting (AWH) has the potential to address water scarcity in arid regions. However, developing adsorbents that effectively capture water at a low relative humidity (RH < 30%) and release it with minimal energy consumption remains a challenge. Herein, we report a fluorophenyl oligomer (FO)-incorporated metal-organic framework (MOF), HKUST-1 (FO@HK), which exhibits fast adsorption kinetics at low RH levels and facile desorption by sunlight. The incorporated fluorophenyl undergoes vapor-phase polymerization at the metal center to generate fluorophenyl oligomers that enhance the hydrolytic stability of FO@HK while preserving its characteristic water sorption behavior. The FO@HK exhibited vapor sorption rates of 8.04 and 11.76 L kg h at 20 and 30% RH, respectively, which are better than the state-of-the-art AWH sorbents. Outdoor tests using a solar-driven large-scale AWH device demonstrate that the sorbent can harvest 264.8 mL of water at a rate of 2.62 L kg per day. This study provides a ubiquitous strategy for transforming water-sensitive MOFs into AWH sorbents.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11557930PMC
http://dx.doi.org/10.1038/s41467-024-53853-7DOI Listing

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