4.7 Article

Expanded Porous MOF-505 Analogue Exhibiting Large Hydrogen Storage Capacity and Selective Carbon Dioxide Adsorption

Journal

INORGANIC CHEMISTRY
Volume 52, Issue 6, Pages 2823-2829

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ic301598n

Keywords

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Funding

  1. Major State Basic Research Development Programs [2011CB808704]
  2. NSFC [21201062, 20931004]
  3. Science Foundation of Innovative Research Team of NSFC [20721002]
  4. Fundamental Research Funds for the Central Universities [1114020501]

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An expanded 4,4-paddlewheel-connected porous MOF-505-type metal-organic framework (MOF), [Cu-2(PDEB)(H2O)(2)].xS (NJU-Bail2; NJU-Bai represents the Nanjing University Bai group and S represents noncoordinated solvent molecules) has been designed from a nanosized rectangular diisophthalate linker containing alkyne groups 5,5'-(1,4-phenylenedi-2,1-ethynediyl)bis(1,3-benzenecarboxylic acid). This MOF material possesses permanent microporosity with the highest Brunauer-Emmett-Teller surface area of 3038 m(2).g(-1) and the largest unsaturated total hydrogen storage capacity of 62.7 mg.g(-1) at 77 K and 20 bar among reported MOF-505 analogues. Additionally, NJU-Bail2 also exhibits excellent carbon dioxide (CO2) uptake capacity (23.83 and 19.85 mmol.g(-1) at 20 bar for 273 and 298 K, respectively) and selective gas adsorption properties with CO2/CH4 selectivity of 5.0 and CO2/N-2 selectivity of 24.6 at room temperature.

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