journal article·2020-01-29Open access

Tuned Hydrogen Bonding in Rare-Earth Metal–Organic Frameworks for Design of Optical and Electronic Properties: An Exemplar Study of Y–2,5-Dihydroxyterephthalic Acid

Dayton J. Vogel, Tina M. Nenoff, Jessica M. Rimsza

Abstract

Organic linkers in metal-organic framework (MOF) materials exhibit differences in hydrogen bonding (H-bonding), which can alter the geometric, electronic, and optical properties of the MOF. Density functional theory (DFT) simulations were performed on a photoluminescent Y-2,5-dihydroxyterephthalic acid (DOBDC) MOF with H-bonding concentrations between 0 and 100%; the H-bonds were located on both bidentate- and monodentate-bound DOBDC linkers. At 0% H-bond concentration in the framework, the lattice parameters contracted, the density increased, and simulated X-ray diffraction patterns shifted. Comparison with published experimental data identified that Y-DOBDC MOF structures must have a degree of H-bond concentration. The concentration of H-bonds in the system shifted the calculated band gap energy from 2.25 eV at 100% to 3.00 eV at 0%. The band gap energies also indicate a distinction of H-bonds formed on bidentate-coordinated linkers compared to those on monodentate linkers. Additionally, when the calculated optical spectra are compared with experimental data, the ligand-to-ligand charge-transfer luminescence in Y-DOBDC MOFs is expected to result from an average of 20-40% H-bonding with at least 50% of the bidentate linkers containing H-bonding. Therefore, the type of H-bonding within the DOBDC linker determines the electronic structure and the optical absorption of the MOF framework structure. Tuning of the H-bonding in rare-earth MOFs provides an opportunity to control the specific optical and adsorption properties of the MOF framework on the basis of reactions between the linker and the environment.
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Research context

OpenAlex topics: Metal-Organic Frameworks: Synthesis and Applications · X-ray Diffraction in Crystallography · Crystal Structures and Properties

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (51)

Show source-provided references
1. 10.1039/b802426j10.1039/b802426j ↗
2. 10.1016/j.jhazmat.2012.11.01110.1016/j.jhazmat.2012.11.011 ↗
3. 10.1021/ja807023q10.1021/ja807023q ↗
4. 10.3390/ma704319810.3390/ma7043198 ↗
5. 10.1021/acs.chemmater.5b0031510.1021/acs.chemmater.5b00315 ↗
6. 10.1021/acs.jpcc.8b0619810.1021/acs.jpcc.8b06198 ↗
7. 10.1039/b802352m10.1039/b802352m ↗
8. 10.1016/j.ccr.2013.10.02310.1016/j.ccr.2013.10.023 ↗
9. 10.1021/acsami.7b0585910.1021/acsami.7b05859 ↗
10. 10.1021/cm500700z10.1021/cm500700z ↗
11. 10.1021/ja211230p10.1021/ja211230p ↗
12. 10.1039/C6TA03065C10.1039/C6TA03065C ↗
13. 10.1021/ic301771b10.1021/ic301771b ↗
14. 10.1039/c0cc02069a10.1039/c0cc02069a ↗
15. 10.1021/acs.inorgchem.6b0057110.1021/acs.inorgchem.6b00571 ↗
16. 10.1021/acs.inorgchem.6b0087810.1021/acs.inorgchem.6b00878 ↗
17. 10.1021/acs.inorgchem.6b0283810.1021/acs.inorgchem.6b02838 ↗
18. 10.1039/C5CP04139B10.1039/C5CP04139B ↗
19. 10.1021/acsami.9b1647010.1021/acsami.9b16470 ↗
20. 10.1103/PhysRevB.47.55810.1103/PhysRevB.47.558 ↗
21. 10.1103/PhysRevB.49.1425110.1103/PhysRevB.49.14251 ↗
22. 10.1016/0927-0256(96)00008-010.1016/0927-0256(96)00008-0 ↗
23. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
24. 10.1103/PhysRevB.50.1795310.1103/PhysRevB.50.17953 ↗
25. 10.1103/PhysRevB.59.175810.1103/PhysRevB.59.1758 ↗
26. 10.1103/PhysRevLett.100.13640610.1103/PhysRevLett.100.136406 ↗
27. 10.1021/acs.jpclett.9b0186710.1021/acs.jpclett.9b01867 ↗
28. 10.1039/C9CP04038B10.1039/C9CP04038B ↗
29. 10.1039/C6CP04056J10.1039/C6CP04056J ↗
30. 10.1039/C7TA10794C10.1039/C7TA10794C ↗
31. 10.1039/C6CP05479J10.1039/C6CP05479J ↗
32. 10.1063/1.338234410.1063/1.3382344 ↗
33. 10.1002/jcc.2175910.1002/jcc.21759 ↗
34. 10.1021/jp511789g10.1021/jp511789g ↗
35. 10.1039/C6CP00768F10.1039/C6CP00768F ↗
36. 10.4028/www.scientific.net/SSP.130.1510.4028/www.scientific.net/SSP.130.15 ↗
37. 10.1063/1.156406010.1063/1.1564060 ↗
38. 10.1063/1.240466310.1063/1.2404663 ↗
39. 10.1021/jp306845g10.1021/jp306845g ↗
40. 10.1021/acs.jpcc.5b0643410.1021/acs.jpcc.5b06434 ↗
41. 10.1021/acs.jpclett.6b0304810.1021/acs.jpclett.6b03048 ↗
42. 10.1021/acs.jpcc.7b0537510.1021/acs.jpcc.7b05375 ↗
43. 10.1021/ct500409310.1021/ct5004093 ↗
44. 10.1103/PhysRevB.75.04512110.1103/PhysRevB.75.045121 ↗
45. 10.1039/B812838C10.1039/B812838C ↗
46. 10.1021/acs.jpclett.6b0180710.1021/acs.jpclett.6b01807 ↗
47. 10.1021/ja411007310.1021/ja4110073 ↗
48. 10.1016/j.matt.2019.02.00210.1016/j.matt.2019.02.002 ↗
49. 10.1021/jp062759o10.1021/jp062759o ↗
50. 10.1016/j.molstruc.2010.05.03910.1016/j.molstruc.2010.05.039 ↗
51. 10.1146/annurev.physchem.48.1.51110.1146/annurev.physchem.48.1.511 ↗