journal article·2021-05-19

Transfer and Amplification of Iodine-Based Diacetylene Amphiphiles to Anisotropic Optical Properties by Uniaxial Orientation in Thin Films

Yu-Jin Choi, Seohee Park, Dong-Gue Kang, Seok-In Lim, Jahyeon Koo, Duy Thanh Tran, Sungjune Park, Kwang-Un Jeong

ACS Applied Materials & Interfaces· Volume 13· Issue 19
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Abstract

For flexible displays, there is a desperate need for a broadband coatable polarizer that can absorb light in a specific direction. Conventional polarizers fabricated by the polymer stretching process are too thick (50–200 μm) to be used as polarizers that can be applied to antireflective films in flexible displays. For the development of the broadband coatable thin film polarizer, diacetylene (DA) amphiphiles containing I– or I3– are newly designed and synthesized, and the content of DA amphiphiles in the 4,6-decadiyne solvent is optimized to form a lyotropic liquid crystal (LLC) phase. Topochemical polymerization of uniaxially oriented iodine-based DA not only stabilizes the film but also broadens the polarization light region from 350 to 700 nm. The transfer and amplification of iodine and DA functions in uniaxially oriented thin films enable the fabrication of broadband coatable thin film polarizers.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Polydiacetylene-based materials and applications · Liquid Crystal Research Advancements · Ocular Surface and Contact Lens

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

Affiliations

Department of Polymer-Nano Science and Technology, Department of Nano Convergence Engineering, Jeonbuk National University, Jeonju 54896, Republic of Korea

Funding

National Cancer Institute · Ministry of Trade, Industry and Energy

References (43)

Show source-provided references
1. 10.1038/nmat245910.1038/nmat2459 ↗
2. 10.1126/sciadv.aax425710.1126/sciadv.aax4257 ↗
3. 10.1021/nn100295x10.1021/nn100295x ↗
4. 10.1021/jacs.7b1019310.1021/jacs.7b10193 ↗
5. 10.1021/ja504157310.1021/ja5041573 ↗
6. 10.1126/science.117703110.1126/science.1177031 ↗
7. 10.1021/acs.macromol.5b0199810.1021/acs.macromol.5b01998 ↗
8. 10.1364/AO.22.00322910.1364/AO.22.003229 ↗
9. 10.1364/JOSA.41.00095710.1364/JOSA.41.000957 ↗
10. 10.1016/j.tsf.2015.07.01610.1016/j.tsf.2015.07.016 ↗
11. 10.1039/C7TC03974C10.1039/C7TC03974C ↗
12. 10.1039/c0jm03882b10.1039/c0jm03882b ↗
13. 10.1021/acsami.5b0999510.1021/acsami.5b09995 ↗
14. 10.1002/adfm.20100254610.1002/adfm.201002546 ↗
15. 10.1002/adfm.20030519410.1002/adfm.200305194 ↗
16. 10.1002/adma.20060035510.1002/adma.200600355 ↗
17. 10.1016/j.polymer.2019.05.03210.1016/j.polymer.2019.05.032 ↗
18. 10.1021/ar700248910.1021/ar7002489 ↗
19. 10.1126/science.269.5223.51510.1126/science.269.5223.515 ↗
20. 10.1021/acs.chemmater.8b0518510.1021/acs.chemmater.8b05185 ↗
21. 10.1002/adma.20200398010.1002/adma.202003980 ↗
22. 10.1002/aenm.20120086010.1002/aenm.201200860 ↗
23. 10.1039/C3TC31366B10.1039/C3TC31366B ↗
24. 10.1021/acs.jpclett.5b0006210.1021/acs.jpclett.5b00062 ↗
25. 10.1039/C0JM02875D10.1039/C0JM02875D ↗
26. 10.1002/adfm.20150484510.1002/adfm.201504845 ↗
27. 10.1021/acs.langmuir.5b0017510.1021/acs.langmuir.5b00175 ↗
28. 10.1002/adfm.20180490610.1002/adfm.201804906 ↗
29. 10.1021/bm400079410.1021/bm4000794 ↗
30. 10.1038/3507354410.1038/35073544 ↗
31. 10.1002/smll.20190134210.1002/smll.201901342 ↗
32. 10.1002/anie.19972601110.1002/anie.199726011 ↗
33. 10.1038/srep3647210.1038/srep36472 ↗
34. 10.1021/acsami.9b0257110.1021/acsami.9b02571 ↗
35. 10.1021/acsami.6b0336410.1021/acsami.6b03364 ↗
36. 10.1002/adfm.20160629410.1002/adfm.201606294 ↗
37. 10.1080/02678290020239010.1080/026782900202390 ↗
38. 10.1021/ac981301i10.1021/ac981301i ↗
39. 10.1002/adfm.20030438510.1002/adfm.200304385 ↗
40. 10.1063/1.11792710.1063/1.117927 ↗
41. 10.1063/1.221999810.1063/1.2219998 ↗
42. 10.1364/OL.39.00514610.1364/OL.39.005146 ↗
43. 10.1002/adfm.20190521410.1002/adfm.201905214 ↗