Selective O2 Sorption at Ambient Temperatures via Node Distortions in Sc-MIL-100
Source abstract
Abstract
An open pored metal–organic framework (MOF) with oxygen selectivity at exceptionally high temperatures is confirmed by synthesis, sorption, and synchrotron structural analyses. The large-pore MIL-100 framework with access to the metal center (e.g., Sc and Fe) resulted in preferential O 2 over N 2 gas uptake at temperatures ranging from 77 K to ambient temperatures (258, 298, and 313 K). Most notably, Sc-MIL-100 shows exceptional O 2 sorption; pair distribution function analyses indicate that this is due to distortions in the framework owing to the size of Sc atoms, in particular in the trimer metal cluster. Experimental studies also correlate very well with GCMC simulations, confirming more favorable O 2 -framework interactions at pressures up to 1 bar, due to the close proximity of O 2 to the high density of metal centers in the small tetrahedral cages. Both materials maintain their crystallinity upon gas adsorption cycling, are regenerable, and show exceptional promise for use in energy efficient oxygen purification processes, such as Pressure Swing Adsorption.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · X-ray Diffraction in Crystallography · Zeolite Catalysis and Synthesis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
X-ray Science Division, Advanced Photon Source, Argonne National Laboratory, Argonne, Illinois 60439, United States
Funding
Laboratory Directed Research and Development · U.S. Department of Energy · National Nuclear Security Administration
References (42)
Show source-provided references
1. 10.1039/C3EE42350F10.1039/C3EE42350F ↗
2. 10.1021/ef301266j10.1021/ef301266j ↗
3. 2008 · 135
4. 10.1080/0149639910805050410.1080/01496399108050504 ↗
5. 10.1016/S1387-1811(03)00353-610.1016/S1387-1811(03)00353-6 ↗
6. 10.1021/cm504229310.1021/cm5042293 ↗
7. 10.1021/jp511789g10.1021/jp511789g ↗
8. 10.1021/ja102792510.1021/ja1027925 ↗
9. 10.1021/ja205976v10.1021/ja205976v ↗
10. 10.1039/b802426j10.1039/b802426j ↗
11. 10.1039/B916295J10.1039/B916295J ↗
12. 10.1021/cr200190s10.1021/cr200190s ↗
13. 10.1039/C4CS00032C10.1039/C4CS00032C ↗
14. 10.1039/C4CS00230J10.1039/C4CS00230J ↗
15. 10.1002/anie.20046059210.1002/anie.200460592 ↗
16. 10.1016/j.micromeso.2010.12.01610.1016/j.micromeso.2010.12.016 ↗
17. 10.1039/B704325B10.1039/B704325B ↗
18. 10.1107/S002188980301756410.1107/S0021889803017564 ↗
19. 10.1107/S002188980700785610.1107/S0021889807007856 ↗
20. 10.1080/0895795960820140810.1080/08957959608201408 ↗
21. Toby B. H. · J. Appl. Crystallogr. · 2003 · 46 · 54410.1107/S0021889813003531 ↗
22. 10.1107/S002188981003049910.1107/S0021889810030499 ↗
23. 10.1107/S002188980100224210.1107/S0021889801002242 ↗
24. 10.1080/08927022.2013.82820810.1080/08927022.2013.828208 ↗
25. 10.1016/j.fluid.2007.07.01410.1016/j.fluid.2007.07.014 ↗
26. 10.1002/aic.69047071910.1002/aic.690470719 ↗
27. 10.1021/ja00051a04010.1021/ja00051a040 ↗
28. 10.1039/C3TB21328E10.1039/C3TB21328E ↗
29. 10.1002/aic.69011012510.1002/aic.690110125 ↗
30. 10.1016/j.cpc.2015.11.01610.1016/j.cpc.2015.11.016 ↗
31. 10.1021/jacs.6b0006910.1021/jacs.6b00069 ↗
32. 10.1107/S010876810200389010.1107/S0108768102003890 ↗
33. 10.1039/C2CY20577G10.1039/C2CY20577G ↗
34. 10.1021/ja202228v10.1021/ja202228v ↗
35. 10.1039/c2dt12138g10.1039/c2dt12138g ↗
36. 10.1021/jz402019d10.1021/jz402019d ↗
37. 10.1016/j.micromeso.2013.01.01210.1016/j.micromeso.2013.01.012 ↗
38. 10.1016/j.micromeso.2014.03.02710.1016/j.micromeso.2014.03.027 ↗
39. 10.1021/la501594t10.1021/la501594t ↗
40. 10.1021/ja505477910.1021/ja5054779 ↗
41. Parkes M. V. · Phys. Chem. Chem. Phys. · 2016 · 18 · 1152810.1039/C6CP00768F ↗
42. 10.1016/j.jcis.2015.06.03610.1016/j.jcis.2015.06.036 ↗