Optical Modulation of Waveguiding in Spiropyran-Functionalized Polydiacetylene Microtube
Source abstract
Abstract
Optical modulation of waveguiding and logic operations play significant roles in highly integrated optical communication components, optical computing, and photonic circuits. Herein, we designed and synthesized spiropyran-functionalized polydiacetylene (SFPDA) microtubes, and realized reversible optical modulation of waveguiding in SFPDA microtubes through fluorescence resonance energy transfer (FRET) between the PDA matrix and spiropyran in open merocyanine (MC) form within the surface of the microtubes. Because of the reversible isomerization characteristics of spiropyran units, we have realized resettable, multireadout logic system that includes OR and INHIBIT logic operations in SFPDA microtube.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Polydiacetylene-based materials and applications · Photoreceptor and optogenetics research · Supramolecular Self-Assembly in Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
CAS Key Laboratory of Soft Matter Chemistry, Department of Polymer Science and Engineering, Key Laboratory of Optoelectronic Science and Technology in Anhui Province, and §Department of Optics and Optical Engineering, University of Science and Technology of China, Hefei, Anhui 230026, P. R. China
Funding
Ministry of Education of the People's Republic of China · Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China · Chinese Academy of Sciences
References (27)
Show source-provided references
1. Yan B. B. · Adv. Mater. · 2009 · 21 · 243610.1002/adma.200803684 ↗
2. Kong Q. H. · J. Am. Chem. Soc. · 2014 · 136 · 238210.1021/ja410069k ↗
3. Gaufres E. · ACS Nano · 2012 · 6 · 381310.1021/nn204924n ↗
4. Zhu D. F. · ACS Nano · 2011 · 5 · 429310.1021/nn103211d ↗
5. Liu M. · Nature · 2011 · 474 · 6410.1038/nature10067 ↗
6. Moon H. · J. Am. Chem. Soc. · 2004 · 126 · 1532210.1021/ja045208p ↗
7. Zhao Y. S. · Acc. Chem. Res. · 2010 · 43 · 40910.1021/ar900219n ↗
8. O’Carroll D. · Small · 2007 · 3 · 117810.1002/smll.200600575 ↗
9. Liao Q. · Adv. Mater. · 2009 · 21 · 415310.1002/adma.200900997 ↗
10. O’Carroll D. · Small · 2007 · 3 · 117810.1002/smll.200600575 ↗
11. Fasano V. · Macromolecules · 2013 · 46 · 593510.1021/ma400145a ↗
12. Liu H. · Small · 2006 · 2 · 49510.1002/smll.200500432 ↗
13. Meng C. · Adv. Mater. · 2011 · 23 · 377010.1002/adma.201101392 ↗
14. Hu W. L. · Adv. Mater. · 2014 · 26 · 313610.1002/adma.201305712 ↗
15. Liang T. K. · Opt. Commun. · 2006 · 265 · 17110.1016/j.optcom.2006.03.031 ↗
16. Xu Q. · Opt Express · 2007 · 15 · 92410.1364/OE.15.000924 ↗
17. Soltani M. · Nat. Nanotechnol. · 2014 · 9 · 44810.1038/nnano.2014.79 ↗
18. Zaghloul Y. A. · Opt Express · 2006 · 14 · 987910.1364/OE.14.009879 ↗
19. Wei H. · Nat. Commun. · 2011 · 2 · 38710.1038/ncomms1388 ↗
20. Kameda M. · Langmuir · 2004 · 20 · 931510.1021/la049649y ↗
21. Xia H. Y. · Macromol. Rapid Commun. · 2014 · 35 · 30310.1002/marc.201300829 ↗
22. Liu D. B. · Angew. Chem., Int. Ed. · 2011 · 50 · 410310.1002/anie.201008198 ↗
23. Zhang S. P. · Phys. Rev. Lett. · 2011 · 107 · 1
24. Barberá J. · J. Am. Chem. Soc. · 2006 · 128 · 448710.1021/ja0585477 ↗
25. Lee J. · Adv. Mater. · 2009 · 21 · 367410.1002/adma.200900639 ↗
26. Ivashenko O. · Langmuir · 2013 · 29 · 429010.1021/la400192c ↗
27. Ivashenko O. · J. Phys. Chem. C · 2013 · 117 · 1856710.1021/jp406458a ↗