Rewritable Polymer Optical Waveguide Chip Based on Photoisomerization Feature of Photosensitive Chromophore
Source abstract
Abstract
The core layer of an optical waveguide device was fabricated by doping the photosensitive chromophore spiropyran derivative SP-Br into poly(methyl methacrylate) (PMMA). The design of the core layer allows us to precisely control the optical property of the waveguide using the photoisomerization process of SP-Br. Under UV excitation, the controllable conversion between SP-Br and the merocyanine isomer MC-Br allows dynamic and continuous changes in the refractive index, thus enabling the function of repeated writing and erasing of optical paths in the optical waveguide device. The ability to dynamically adjust the refractive index provides unprecedented flexibility in the design and fabrication of an optical waveguide device.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Photonic and Optical Devices · Photonic Crystals and Applications · Photochromic and Fluorescence Chemistry
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Materials Science and Engineering
Changchun University of Science and Technology
State Key Laboratory of Integrated Optoelectronics, JLU Region, College of Electronic Science and Engineering
Jilin University
Chongqing Research Institute
Engineering Research Center for Optoelectronic Functional Materials
Ministry of Education
Funding
Natural Science Foundation of Chongqing Municipality · Education Department of Jilin Province
References (39)
Show source-provided references
1. 10.1002/adom.20240151810.1002/adom.202401518 ↗
2. 10.1016/j.optmat.2006.08.00110.1016/j.optmat.2006.08.001 ↗
3. 10.1039/C9TC00749K10.1039/C9TC00749K ↗
4. 10.1038/s41467-018-07269-910.1038/s41467-018-07269-9 ↗
5. 10.1002/adom.20180051010.1002/adom.201800510 ↗
6. 10.1016/j.rinp.2018.06.02610.1016/j.rinp.2018.06.026 ↗
7. 10.1109/JSTQE.2016.253728310.1109/JSTQE.2016.2537283 ↗
8. 10.1109/JLT.2019.294349410.1109/JLT.2019.2943494 ↗
9. 10.1002/adma.20180158410.1002/adma.201801584 ↗
10. 10.3390/polym1010108610.3390/polym10101086 ↗
11. 10.1002/1521-4095(20021002)14:19<1339::AID-ADMA1339>3.0.CO;2-O10.1002/1521-4095(20021002)14:19<1339::AID-ADMA1339>3.0.CO;2-O ↗
12. 10.1007/s11426-018-9406-110.1007/s11426-018-9406-1 ↗
13. 10.1002/anie.20170429410.1002/anie.201704294 ↗
14. 10.1016/j.compositesb.2017.04.01910.1016/j.compositesb.2017.04.019 ↗
15. 10.1021/acs.nanolett.3c0331710.1021/acs.nanolett.3c03317 ↗
16. 10.1038/ncomms1037410.1038/ncomms10374 ↗
17. 10.1002/anie.20181042210.1002/anie.201810422 ↗
18. 10.1002/adom.20220119510.1002/adom.202201195 ↗
19. 10.1038/s41377-024-01383-810.1038/s41377-024-01383-8 ↗
20. 10.1002/anie.20180627210.1002/anie.201806272 ↗
21. 10.1002/anie.20160840810.1002/anie.201608408 ↗
22. 10.1039/C9GC01235D10.1039/C9GC01235D ↗
23. 10.1002/adfm.20231293010.1002/adfm.202312930 ↗
24. 10.1038/s41467-017-02715-610.1038/s41467-017-02715-6 ↗
25. 10.1021/acsami.3c0677410.1021/acsami.3c06774 ↗
26. 10.1016/j.progpolymsci.2017.11.00110.1016/j.progpolymsci.2017.11.001 ↗
27. 10.1039/D1CS90005F10.1039/D1CS90005F ↗
28. 10.1002/adfm.20230376510.1002/adfm.202303765 ↗
29. 10.1016/j.jcis.2024.03.12910.1016/j.jcis.2024.03.129 ↗
30. 10.1007/s12200-024-00124-410.1007/s12200-024-00124-4 ↗
31. 10.1016/j.aca.2020.01.05710.1016/j.aca.2020.01.057 ↗
32. 10.1016/j.jphotochem.2023.11509810.1016/j.jphotochem.2023.115098 ↗
33. 10.1002/marc.20230036010.1002/marc.202300360 ↗
34. 10.1039/D3CC01505J10.1039/D3CC01505J ↗
35. 10.1103/PhysRevB.104.08530710.1103/PhysRevB.104.085307 ↗
36. 10.1021/jacs.0c0220110.1021/jacs.0c02201 ↗
37. 10.1021/cr60136a00410.1021/cr60136a004 ↗
38. 10.1016/j.colsurfa.2022.13001810.1016/j.colsurfa.2022.130018 ↗
39. 10.1002/adfm.20240188010.1002/adfm.202401880 ↗