Postsynthetic Metalation of a New Metal–Organic Framework To Improve Methane Working Storage Capacity
Source abstract
Abstract
In the design of metal–organic frameworks (MOFs) for methane storage, a balance must be struck between the porosity of the MOF, the internal pore environment, the adsorption thermodynamics, and the density. Herein, we report the design of a new Zr-MOF, termed MOF-700, which was metalated with various Cu(II) salts to produce an isoreticular series of three new, highly porous MOFs (MOF-701, MOF-702, and MOF-703). The position of the metalated sites was determined by X-ray absorption spectroscopy, and the metalated frameworks were found to display high volumetric methane storage working capacities [206 cm3(STP) cm–3 at 298 K and 5.0–80.0 bar for MOF-701]. This constitutes an improvement of 50% over the performance of the parent MOF-700 [137 cm3(STP) cm–3] and highlights the prospect of optimization of methane working storage capacity by postsynthetic metalation.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · Covalent Organic Framework Applications · Carbon dioxide utilization in catalysis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Center for Innovative Materials and Architectures (INOMAR), Vietnam National University─Hochiminh, Hochiminh City 721337, Vietnam
Department of Chemistry, University of California─Berkeley, Berkeley, California 94720, United States
Materials Discovery Research Unit, Advanced Research Centre, Royal Scientific Society, Amman 11941, Jordan
Funding
Viet Nam National University Ho Chi Minh City
References (31)
Show source-provided references
1. Yaghi, O. M.; Kalmutzki, M. J.; Diercks, C. S. Introduction to Reticular Chemistry: Metal-Organic Frameworks and Covalent Organic Frameworks; Wiley-VCH: Weinheim, Germany, 2019; p 509.10.1002/9783527821099 ↗
2. 10.1002/anie.19971725110.1002/anie.199717251 ↗
3. 10.1016/j.ccr.2017.10.00210.1016/j.ccr.2017.10.002 ↗
4. 10.1126/science.106720810.1126/science.1067208 ↗
5. 10.1002/anie.20100758310.1002/anie.201007583 ↗
6. 10.1002/anie.20151100610.1002/anie.201511006 ↗
7. 10.1021/ja501810r10.1021/ja501810r ↗
8. 10.1002/anie.20170497410.1002/anie.201704974 ↗
9. 10.1021/jacs.7b0545310.1021/jacs.7b05453 ↗
10. 10.1021/jacs.7b0132010.1021/jacs.7b01320 ↗
11. 10.1021/jacs.6b0526110.1021/jacs.6b05261 ↗
12. 10.1016/j.ccr.2022.21464410.1016/j.ccr.2022.214644 ↗
13. 10.1021/jacs.8b1138610.1021/jacs.8b11386 ↗
14. 10.1021/ja501826710.1021/ja5018267 ↗
15. 10.1021/cm301427w10.1021/cm301427w ↗
16. 10.1021/jp506561610.1021/jp5065616 ↗
17. 10.1038/ncomms1261010.1038/ncomms12610 ↗
18. 10.1038/nature1573210.1038/nature15732 ↗
19. 10.1038/s41467-019-10185-110.1038/s41467-019-10185-1 ↗
20. 10.1021/jacs.7b0834710.1021/jacs.7b08347 ↗
21. 10.1039/C3SC52633J10.1039/C3SC52633J ↗
22. 10.1002/adma.20170479210.1002/adma.201704792 ↗
23. 10.1002/anie.20180082010.1002/anie.201800820 ↗
24. 10.1038/nmat505010.1038/nmat5050 ↗
25. Methane Opportunities for Vehicular Energy, Advanced Research Project Agency–Energy, U.S. Dept. of Energy, Funding Opportunity No. DE-FOA-0000672, 2012.
26. 10.1021/jacs.5b0665710.1021/jacs.5b06657 ↗
27. 10.1007/s12274-020-2794-910.1007/s12274-020-2794-9 ↗
28. 10.1021/acs.jced.1c0095110.1021/acs.jced.1c00951 ↗
29. 10.1039/C5CS00837A10.1039/C5CS00837A ↗
30. 10.1039/D1TA06828H10.1039/D1TA06828H ↗
31. 10.1021/acs.inorgchem.2c0113010.1021/acs.inorgchem.2c01130 ↗