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Porous metal–organic polyhedral frameworks with optimal molecular dynamics and pore geometry for methane storage

Yan, Yong; Kolokolov, Daniil I.; da Silva, Ivan; Stepanov, Alexander G.; Blake, Alexander J.; Dailly, Anne; Manuel, Pascal; Tang, Chiu C.; Yang, Sihai; Schröder, Martin

Authors

Yong Yan

Daniil I. Kolokolov

Ivan da Silva

Alexander G. Stepanov

Alexander J. Blake

Anne Dailly

Pascal Manuel

Chiu C. Tang

Sihai Yang

Martin Schröder



Abstract

Natural gas (methane, CH4) is widely considered as a promising energy carrier for mobile applications. Maximising the storage capacity is the primary goal for the design of future storage media. Here we report the CH4 storage properties in a family of isostructural (3,24)-connected porous materials, MFM-112a, MFM-115a and MFM-132a with different linker backbone functionalisation. Both MFM-112a and MFM-115a show excellent CH4 uptakes of 236 and 256 cm3 (STP) cm–3 (v/v) at 80 bar and room temperature, respectively. Significantly, MFM-115a displays an exceptionally high deliverable CH4 capacity of 208 v/v between 5 and 80 bar at room temperature, making it among the best performing MOFs for methane storage. We also synthesized the partially deuterated versions of the above materials and applied solid-state 2H NMR spectroscopy to show that these three frameworks contain molecular rotors which exhibit motion in fast, medium and slow regimes, respectively. In situ neutron powder diffraction studies on the binding sites for CD4 within MFM-132a and MFM-115a reveal that the primary binding site is located within the small pocket enclosed by the [(Cu2)3(isophthalate)3] window and three anthracene/phenyl panels. The open Cu(II) sites are the secondary/tertiary adsorption sites in these structures. Thus, we obtained direct experimental evidence showing that a tight cavity can generate a stronger binding affinity to gas molecules than open metal sites. Thus, solid-state 2H NMR and neutron diffraction studies revealed that it is the combination of optimal molecular dynamics, pore geometry and size, and favourable binding sites that leads to the exceptional and different methane uptakes in these materials.

Journal Article Type Article
Publication Date Sep 27, 2017
Journal Journal of the American Chemical Society
Print ISSN 0002-7863
Electronic ISSN 1520-5126
Publisher American Chemical Society
Peer Reviewed Peer Reviewed
Volume 139
Issue 38
Pages 13349-13360
APA6 Citation Yan, Y., Kolokolov, D. I., da Silva, I., Stepanov, A. G., Blake, A. J., Dailly, A., …Schröder, M. (2017). Porous metal–organic polyhedral frameworks with optimal molecular dynamics and pore geometry for methane storage. Journal of the American Chemical Society, 139(38), 13349-13360. https://doi.org/10.1021/jacs.7b05453
DOI https://doi.org/10.1021/jacs.7b05453
Publisher URL http://pubs.acs.org/doi/abs/10.1021/jacs.7b05453
Copyright Statement Copyright information regarding this work can be found at the following address: http://creativecommons.org/licenses/by/4.0

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Copyright Statement
Copyright information regarding this work can be found at the following address: http://creativecommons.org/licenses/by/4.0





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