Complexing Eu3+/Tb3+ in a Nanoscale Postmodified Zr-MOF toward Temperature-Modulated Multispectrum Chromism
Source abstract
Abstract
In recent years, extensive research has been directed toward the successful preparation of nanoscale luminescent thermometers with high sensitivities operative in a broad temperature range. To achieve this goal, we have devised a unique design and facile multistep synthesis of Zr-ctpy-NMOF@TbxEuy compounds by confining Ln-complexes (Ln = Eu3+/Tb3+) into a robust nanoscale Zr-NMOF (MOF-808) via postsynthetic modification. Covalent grafting of 4-(4′-carboxyphenyl)-2,2′:6,2″terpyridine ligand (ctpy) with a high triplet state energy and corresponding immobilization of bimetallic Ln3+ ions resulted in yellow light-emitting Zr-ctpy-NMOF@Tb1.66Eu0.14 to achieve a sensitivity of 5.2% K–1 (thermal uncertainty dT < 1 K) operative over a broad temperature range of 25–400 K. To defeat the odds related to the detection of minute temperature changes using luminescent materials, we prepared a white light-emitting Zr-ctpy-NMOF@Tb1.4Eu0.31 that showed temperature-modulated multispectrum chromism where the color drastically changes from green (at 25 K, Q.Y.: 20.21%) to yellowish-green (at 200 K, Q.Y.: 23.13%) to white (at 300 K, Q.Y.: 26.4%) to orange (at 350 K, Q.Y.: 26.93%) and finally red (at 400 K, Q.Y.: 28.2%) with a high energy transfer efficiency of 49.8%, which is further supported by electron–phonon coupling.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Luminescence Properties of Advanced Materials · Metal-Organic Frameworks: Synthesis and Applications · Lanthanide and Transition Metal Complexes
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (69)
Show source-provided references
1. 10.1002/anie.20110239010.1002/anie.201102390 ↗
2. 10.1039/c2nr30663h10.1039/c2nr30663h ↗
3. 10.1002/chem.20160086010.1002/chem.201600860 ↗
4. 10.1002/ejic.20150119510.1002/ejic.201501195 ↗
5. 10.1002/adma.20150101410.1002/adma.201501014 ↗
6. 10.1002/anie.20201337710.1002/anie.202013377 ↗
7. 10.1021/ja210803610.1021/ja2108036 ↗
8. 10.1039/c2nr30764b10.1039/c2nr30764b ↗
9. 10.1039/D0TC03430D10.1039/D0TC03430D ↗
10. 10.1002/anie.20210933610.1002/anie.202109336 ↗
11. 10.1039/C4CC05991C10.1039/C4CC05991C ↗
12. 10.1039/C9SC03916C10.1039/C9SC03916C ↗
13. 10.1021/ja407219k10.1021/ja407219k ↗
14. 10.1021/acs.inorgchem.9b0008410.1021/acs.inorgchem.9b00084 ↗
15. 10.1002/adfm.20150051810.1002/adfm.201500518 ↗
16. 10.1021/acs.inorgchem.0c0062510.1021/acs.inorgchem.0c00625 ↗
17. 10.1039/C5CC07783D10.1039/C5CC07783D ↗
18. 10.1016/j.ccr.2021.21405010.1016/j.ccr.2021.214050 ↗
19. 10.1002/anie.20191398310.1002/anie.201913983 ↗
20. 10.1039/C4CC07038K10.1039/C4CC07038K ↗
21. 10.1039/D0EE03643A10.1039/D0EE03643A ↗
22. 10.1007/s12039-020-01797-y10.1007/s12039-020-01797-y ↗
23. 10.1002/anie.20120416010.1002/anie.201204160 ↗
24. 10.1039/D0CS00955E10.1039/D0CS00955E ↗
25. 10.1038/s41467-017-02600-210.1038/s41467-017-02600-2 ↗
26. 10.1038/s41598-021-96001-710.1038/s41598-021-96001-7 ↗
27. 10.1039/C6TC05316E10.1039/C6TC05316E ↗
28. 10.1016/0022-2313(95)00145-X10.1016/0022-2313(95)00145-X ↗
29. 10.1021/acsanm.1c0337610.1021/acsanm.1c03376 ↗
30. 10.12693/APhysPolA.90.10910.12693/APhysPolA.90.109 ↗
31. 10.1021/ja507119n10.1021/ja507119n ↗
32. 10.1039/C8NJ06362A10.1039/C8NJ06362A ↗
33. 10.1021/acssuschemeng.0c0448610.1021/acssuschemeng.0c04486 ↗
34. 10.1039/b709557k10.1039/b709557k ↗
35. 10.1021/ic300916e10.1021/ic300916e ↗
36. 10.3390/molecules2601008710.3390/molecules26010087 ↗
37. 10.1039/C3CC47225F10.1039/C3CC47225F ↗
38. You B. · Bull. Korean Chem. Soc · 2001 · 22 · 1005
39. 10.1002/advs.20180171510.1002/advs.201801715 ↗
40. 10.1002/slct.20160155810.1002/slct.201601558 ↗
41. 10.1021/om401151p10.1021/om401151p ↗
42. 10.3390/molecules2424451910.3390/molecules24244519 ↗
43. 10.1039/C8PP00108A10.1039/C8PP00108A ↗
44. 10.1016/j.jcat.2020.06.01510.1016/j.jcat.2020.06.015 ↗
45. 10.1021/acs.inorgchem.6b0302410.1021/acs.inorgchem.6b03024 ↗
46. 10.1039/c3tc30205a10.1039/c3tc30205a ↗
47. 10.1039/c2ce25179e10.1039/c2ce25179e ↗
48. 10.1016/j.elspec.2005.08.00310.1016/j.elspec.2005.08.003 ↗
49. 10.1039/D1DT01860D10.1039/D1DT01860D ↗
50. 10.1039/D0SC05721E10.1039/D0SC05721E ↗
51. 10.1016/j.jphotochem.2018.02.02810.1016/j.jphotochem.2018.02.028 ↗
52. 10.1002/advs.20180171510.1002/advs.201801715 ↗
53. 10.1021/acsami.6b1246910.1021/acsami.6b12469 ↗
54. 10.1038/ncomms371710.1038/ncomms3717 ↗
55. 10.1021/ja500686610.1021/ja5006866 ↗
56. 10.1021/am502855510.1021/am5028555 ↗
57. 10.1002/chem.20170553210.1002/chem.201705532 ↗
58. 10.1021/acs.inorgchem.7b0100210.1021/acs.inorgchem.7b01002 ↗
59. 10.1002/anie.20161216010.1002/anie.201612160 ↗
60. 10.1002/chem.20060012410.1002/chem.200600124 ↗
61. 10.1016/j.ccr.2014.03.03510.1016/j.ccr.2014.03.035 ↗
62. 10.1039/C4NR06873D10.1039/C4NR06873D ↗
63. 10.1039/D1TC01532J10.1039/D1TC01532J ↗
64. 10.1021/acs.inorgchem.8b0174610.1021/acs.inorgchem.8b01746 ↗
65. 10.1021/acs.inorgchem.1c0112310.1021/acs.inorgchem.1c01123 ↗
66. 10.1039/C7CS00053G10.1039/C7CS00053G ↗
67. 10.1021/jacs.9b1144310.1021/jacs.9b11443 ↗
68. 10.1021/ja047905n10.1021/ja047905n ↗
69. 10.1063/1.326685010.1063/1.3266850 ↗