4.7 Article

Defect Creation by Linker Fragmentation in Metal-Organic Frameworks and Its Effects on Gas Uptake Properties

Journal

INORGANIC CHEMISTRY
Volume 53, Issue 13, Pages 6914-6919

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ic500722n

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Funding

  1. U.S. Department of Energy [DE-FG02-08ER46522]
  2. DOE ARPA-E
  3. Stanford Global Climate and Energy Project
  4. U.S. Department of Energy (DOE) [DE-FG02-08ER46522] Funding Source: U.S. Department of Energy (DOE)

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We successfully demonstrate an approach based on linker fragmentation to create defects and tune the pore volumes and surface areas of two metal-organic frameworks, NU-125 and HKUST-1, both of which feature copper paddlewheel nodes. Depending on the linker fragment composition, the defect can be either a vacant site or a functional group that the original linker does not have. In the first case, we show that both surface area and pore volume increase, while in the second case they decrease. The effect of defects on the high-pressure gas uptake is also studied over a large temperature and pressure range for different gases. We found that despite an increase in pore volume and surface area in structures with vacant sites, the absolute adsorption for methane decreases for HKUST-1 and slightly increases for NU-125. However, the working capacity (deliverable amount between 65 and 5 bar) in both cases remains similar to parent frameworks due to lower uptakes at low pressures. In the case of NU-125, the effect of defects became more pronounced at lower temperatures, reflecting the greater surface areas and pore volumes of the altered forms.

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