journal article·2022-06

Interface Engineering of Bi‐Fluorescence Molecules for High‐Performance Data Encryption and Ultralow UV‐Light Detection

Jian‐Xin Wang, Luis Gutiérrez‐Arzaluz, Jun Yin, Partha Maity, Yang Zhou, Cailing Chen, Yu Han, Osman M. Bakr, Mohamed Eddaoudi, Omar F. Mohammed

Advanced Optical Materials· Volume 10· Issue 12
Publisher page

Abstract

Abstract It is extremely difficult if not impossible to effectively and precisely regulate the luminescence of organic chromophores from different electronic excited states through external stimuli for use in light‐conversion devices. This is mainly due to the difficulty in breaking Kasha's rule by large energy separation and stabilization of different emissive electronic excited states. Here, the authors address this great challenge in a single experiment by expanding the utility of a monounsaturated omega‐9 fatty acid (oleic acid) capped with organic chromophores as a new and efficient luminescent regulator. More specifically, the authors have successfully promoted the use of oleic acid as an efficient and reversible switch that can precisely regulate chromophore luminescence. These time‐resolved absorption and luminescence experiments, along with density functional theory calculations have clearly demonstrated that ultrafast electron transfer from oleic acid to the difluoroboron β‐diketonate (DFBK) chromophores efficiently blocks the intramolecular charge transfer process of DFBK chromophores, and activates the locally excited state luminescence, leading to different emission colors from different electronic excited states for ultralow UV‐light detection and high‐performance data encryption.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Organic Light-Emitting Diodes Research · Molecular Sensors and Ion Detection

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

Affiliations

Advanced Membranes and Porous Materials Center Division of Physical Science and Engineering King Abdullah University of Science and Technology Thuwal 23955‐6900 Kingdom of Saudi Arabia

KAUST Catalysis Center Division of Physical Science and Engineering King Abdullah University of Science and Technology Thuwal 23955‐6900 Kingdom of Saudi Arabia

Funding

King Abdullah University of Science and Technology

References (61)

Show source-provided references
1. 10.1039/D1CS00198A10.1039/D1CS00198A ↗
2. 10.1126/sciadv.abf966810.1126/sciadv.abf9668 ↗
3. 10.1021/jacs.1c0216910.1021/jacs.1c02169 ↗
4. 10.1038/s41566-019-0408-410.1038/s41566-019-0408-4 ↗
5. 10.1038/s41566-021-00763-510.1038/s41566-021-00763-5 ↗
6. 10.1021/jacs.0c1323510.1021/jacs.0c13235 ↗
7. 10.1021/acs.jpclett.1c0107710.1021/acs.jpclett.1c01077 ↗
8. 10.1021/jacs.1c0127910.1021/jacs.1c01279 ↗
9. 10.1002/anie.20200114110.1002/anie.202001141 ↗
10. 10.1039/C9CC03232K10.1039/C9CC03232K ↗
11. 10.1038/s41566-020-00744-010.1038/s41566-020-00744-0 ↗
12. 10.1002/marc.20220001710.1002/marc.202200017 ↗
13. 10.1016/j.chempr.2020.04.02110.1016/j.chempr.2020.04.021 ↗
14. 10.1002/anie.20190289010.1002/anie.201902890 ↗
15. 10.1021/jacs.1c0927210.1021/jacs.1c09272 ↗
16. 10.1021/acsami.1c2475910.1021/acsami.1c24759 ↗
17. 10.1038/s41467-017-00362-510.1038/s41467-017-00362-5 ↗
18. 10.1038/nchem.261210.1038/nchem.2612 ↗
19. 10.1039/df950090001410.1039/df9500900014 ↗
20. 10.1038/s41557-020-0430-710.1038/s41557-020-0430-7 ↗
21. 10.1016/j.chempr.2018.10.00110.1016/j.chempr.2018.10.001 ↗
22. 10.1002/adma.20200781110.1002/adma.202007811 ↗
23. 10.1038/s41557-021-00697-z10.1038/s41557-021-00697-z ↗
24. 10.1021/acs.jpca.1c0056910.1021/acs.jpca.1c00569 ↗
25. 10.1002/adma.20200805510.1002/adma.202008055 ↗
26. 10.1002/anie.20210160610.1002/anie.202101606 ↗
27. 10.1002/anie.20210146810.1002/anie.202101468 ↗
28. 10.1021/jacs.1c0157110.1021/jacs.1c01571 ↗
29. 10.1016/j.chempr.2019.12.01510.1016/j.chempr.2019.12.015 ↗
30. 10.1016/j.matt.2021.11.01210.1016/j.matt.2021.11.012 ↗
31. 10.1007/s12274-020-2781-110.1007/s12274-020-2781-1 ↗
32. 10.3390/foods1003068510.3390/foods10030685 ↗
33. 10.3389/fphar.2021.69073610.3389/fphar.2021.690736 ↗
34. 10.1093/ajcn/32.11.219810.1093/ajcn/32.11.2198 ↗
35. 10.1016/j.matt.2020.05.00410.1016/j.matt.2020.05.004 ↗
36. 10.1016/j.matt.2021.07.01810.1016/j.matt.2021.07.018 ↗
37. 10.1016/j.chempr.2020.02.01610.1016/j.chempr.2020.02.016 ↗
38. 10.1016/j.fcr.2016.04.00510.1016/j.fcr.2016.04.005 ↗
39. 10.1002/aocs.1217710.1002/aocs.12177 ↗
40. 10.31635/ccschem.020.20190006310.31635/ccschem.020.201900063 ↗
41. 10.31635/ccschem.020.20200015810.31635/ccschem.020.202000158 ↗
42. 10.1021/jacs.0c0200710.1021/jacs.0c02007 ↗
43. 10.1021/acsnano.1c0015610.1021/acsnano.1c00156 ↗
44. 10.1039/D1CC01788H10.1039/D1CC01788H ↗
45. 10.1039/D0CC01505A10.1039/D0CC01505A ↗
46. 10.1021/acs.jpca.0c0864910.1021/acs.jpca.0c08649 ↗
47. 10.1038/nmat250910.1038/nmat2509 ↗
48. 10.1002/adma.20180081710.1002/adma.201800817 ↗
49. 10.1021/ja072025510.1021/ja0720255 ↗
50. 10.1021/ja203206g10.1021/ja203206g ↗
51. 10.1016/j.ccr.2017.06.02610.1016/j.ccr.2017.06.026 ↗
52. 10.1021/acs.jpclett.2c0016810.1021/acs.jpclett.2c00168 ↗
53. 10.1021/acsenergylett.1c0217310.1021/acsenergylett.1c02173 ↗
54. 10.1016/j.jphotochem.2017.10.03610.1016/j.jphotochem.2017.10.036 ↗
55. 10.1021/jacs.7b0055110.1021/jacs.7b00551 ↗
56. 10.1002/polb.2329810.1002/polb.23298 ↗
57. 10.1063/1.181787310.1063/1.1817873 ↗
58. 10.1063/1674-0068/31/cjcp180717110.1063/1674-0068/31/cjcp1807171 ↗
59. 10.1039/C9TC00749K10.1039/C9TC00749K ↗
60. 10.1002/adom.20160062310.1002/adom.201600623 ↗
61. 10.1002/admt.20170028810.1002/admt.201700288 ↗