Isotope-selective pore opening in a flexible metal-organic framework

Author:

Bondorf Linda1ORCID,Fiorio Jhonatan Luiz2ORCID,Bon Volodymyr2ORCID,Zhang Linda1ORCID,Maliuta Mariia2,Ehrling Sebastian2ORCID,Senkovska Irena2ORCID,Evans Jack D.23ORCID,Joswig Jan-Ole2ORCID,Kaskel Stefan2ORCID,Heine Thomas245ORCID,Hirscher Michael1ORCID

Affiliation:

1. Max Planck Institute for Intelligent Systems, Heisenbergstrasse 3, D-70569 Stuttgart, Germany.

2. Technische Universität Dresden, School of Science, Faculty of Chemistry and Food Chemistry, Mommsenstr. 13, 01069 Dresden, Germany.

3. Centre for Advanced Nanomaterials and Department of Chemistry, The University of Adelaide, North Terrace, Adelaide, South Australia 5000, Australia.

4. Helmholtz-Center Dresden-Rossendorf, Leipzig Research Site, Permoserstr. 15, 04138 Leipzig, Germany .

5. Department of Chemistry, Yonsei University, Seodaemun-gu, Seoul 120-749, Republic of Korea.

Abstract

Flexible metal-organic frameworks that show reversible guest-induced phase transitions between closed and open pore phases have enormous potential for highly selective, energy-efficient gas separations. Here, we present the gate-opening process of DUT-8(Ni) that selectively responds to D 2 , whereas no response is observed for H 2 and HD. In situ neutron diffraction directly reveals this pressure-dependent phase transition. Low-temperature thermal desorption spectroscopy measurements indicate an outstanding D 2 -over-H 2 selectivity of 11.6 at 23.3 K, with high D 2 uptake. First-principles calculations coupled with statistical thermodynamics predict the isotope-selective gate opening, rationalized by pronounced nuclear quantum effects. Simulations suggest DUT-8(Ni) to remain closed in the presence of HT, while it also opens for DT and T 2 , demonstrating gate opening as a highly effective approach for isotopolog separation.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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