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Updated: Jul 14, 2025

Synthesis and Characterization of Functionalized Metal-organic Frameworks
Published on: September 5, 2014
Enhanced atmospheric water harvesting efficiency through green-synthesized MOF-801: a comparative study with
Mohammad Aghajani Hashjin1, Shadi Zarshad1, Hosein Banna Motejadded Emrooz2
1Nanotechnology Department, School of Advanced Technologies, Iran University of Science and Technology (IUST), Narmak, Tehran, 16846, Iran.
Abstract:
Adsorption-based atmospheric water harvesting has emerged as a compelling solution in response to growing global water demand. In this context, Metal-organic frameworks (MOFs) have garnered considerable interest due to their unique structure and intrinsic porosity. Here, MOF 801 was synthesized using two different methods: solvothermal and green room temperature synthesis. Comprehensive characterization indicated the formation of MOF-801 with high phase purity, small crystallite size, and excellent thermal stability. Nitrogen adsorption-desorption analysis revealed that green-synthesized MOF-801 possessed an 89% higher specific surface area than its solvothermal-synthesized counterpart. Both adsorbents required activation at a minimum temperature of 90 °C for optimal adsorption performance. Additionally, green-synthesized MOF-801 demonstrated superior adsorption performance compared to solvothermal-synthesized MOF-801, attributed to its small crystal size (around 66 nm), more hydrophilic functional groups, greater specific surface area (691.05 m2/g), and the possibility of having a higher quantity of defects. The maximum water adsorption capacity in green-synthesized MOF-801 was observed at 25 °C and 80% relative humidity, with a value of 41.1 g/100 g, a 12% improvement over the solvothermal-synthesized MOF-801. Remarkably, even at a 30% humidity level, green-synthesized MOF-801 displayed a considerable adsorption capacity of 31.5 g/100 g. Importantly, MOF-801 exhibited long-term effectiveness in multiple adsorption cycles without substantial efficiency decline.

