A partially interpenetrated metal-organic framework for selective hysteretic sorption of carbon dioxide

Sihai Yang*, Xiang Lin, William Lewis, Mikhail Suetin, Elena Bichoutskaia, Julia E. Parker, Chiu C. Tang, David R. Allan, Pierre J. Rizkallah, Peter Hubberstey, Neil R. Champness, K. Mark Thomas, Alexander J. Blake, Martin Schröder

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

339 Scopus citations

Abstract

The selective capture of carbon dioxide in porous materials has potential for the storage and purification of fuel and flue gases. However, adsorption capacities under dynamic conditions are often insufficient for practical applications, and strategies to enhance CO2-host selectivity are required. The unique partially interpenetrated metal-organic framework NOTT-202 represents a new class of dynamic material that undergoes pronounced framework phase transition on desolvation. We report temperature-dependent adsorption/desorption hysteresis in desolvated NOTT-202a that responds selectively to CO2. The CO2 isotherm shows three steps in the adsorption profile at 195 K, and stepwise filling of pores generated within the observed partially interpenetrated structure has been modelled by grand canonical Monte Carlo simulations. Adsorption of N2, CH4, O2, Ar and H2 exhibits reversible isotherms without hysteresis under the same conditions, and this allows capture of gases at high pressure, but selectively leaves CO2 trapped in the nanopores at low pressure.

Original languageEnglish (US)
Pages (from-to)710-716
Number of pages7
JournalNature Materials
Volume11
Issue number8
DOIs
StatePublished - Jan 1 2012

ASJC Scopus subject areas

  • Chemistry(all)
  • Materials Science(all)
  • Condensed Matter Physics
  • Mechanics of Materials
  • Mechanical Engineering

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