Reticular Chemistry in Action: A Hydrolytically Stable MOF Capturing Twice Its Weight in Adsorbed Water
AuthorsTowsif Abtab, Sk Md
Weselinski, Lukasz Jan
Alsadun, Norah Sadun
Hedhili, Mohamed N.
KAUST DepartmentAdvanced Membranes and Porous Materials Research Center
Chemical Engineering Program
Chemical Science Program
Functional Materials Design, Discovery and Development (FMD3)
Imaging and Characterization Core Lab
Physical Science and Engineering (PSE) Division
Online Publication Date2018-01-11
Print Publication Date2018-01
Permanent link to this recordhttp://hdl.handle.net/10754/626981
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AbstractSummary Hydrolytically stable adsorbents, with notable water uptake, are of prime importance and offer great potential for many water-adsorption-related applications. Nevertheless, deliberate construction of tunable porous solids with high porosity and high stability remains challenging. Here, we present the successful deployment of reticular chemistry to address this demand: we constructed Cr-soc-MOF-1, a chemically and hydrolytically stable chromium-based metal-organic framework (MOF) with underlying soc topology. Prominently, Cr-soc-MOF-1 offers the requisite thermal and chemical stability concomitant with unique adsorption properties, namely extraordinary high porosity (apparent surface area of 4,549 m2/g) affording a water vapor uptake of 1.95 g/g at 70% relative humidity. This exceptional water uptake is maintained over more than 100 adsorption-desorption cycles. Markedly, the adsorbed water can be fully desorbed by just the simple reduction of the relative humidity at 25°C. Cr-soc-MOF-1 offers great potential for use in applications pertaining to water vapor control in enclosed and confined spaces and dehumidification.
CitationTowsif Abtab SM, Alezi D, Bhatt PM, Shkurenko A, Belmabkhout Y, et al. (2018) Reticular Chemistry in Action: A Hydrolytically Stable MOF Capturing Twice Its Weight in Adsorbed Water. Chem 4: 94–105. Available: http://dx.doi.org/10.1016/j.chempr.2017.11.005.
SponsorsResearch reported in this publication was fully supported by the King Abdullah University of Science and Technology.