journal article·2015-10

Light polarization states of a cholesteric liquid crystal probed with optical ellipsometry

Eralci M. Therézio, Silésia F.C. da Silva, Gustavo G. Dalkiranis, Paulo Alliprandini Filho, George C. Santos, Fernando Ely, Ivan H. Bechtold, Alexandre Marletta

Optical Materials· Volume 48
Publisher page

Abstract

Abstract Herein a useful methodology to study optical properties of cholesteric liquid crystals (Ch-LC) is proposed by using the Fourier decomposition ellipsometry technique to calculate the Stokes parameters of transmitted and reflected light in the UV–Vis spectral range. Combining Bragg reflection and optical activity we were able to obtain ∼100% of linear or circular light polarization from the Ch-LC sample using achromatic and non-polarized light source. The photonic bandgap and the polarization components can be controlled with the temperature as a result of alterations in the helix pitch of the cholesteric phase. Finally, it is demonstrated the correlation between the dissymmetry factor ( g ) calculated via the Stokes parameter S 3 and the reflection spectrum. The data revealed that the maximum value of S 3 is not coincident with the peak of maximum reflection. The reflected or transmitted light analysis via Stokes parameters obtained by ellipsometry showed an alternative and low cost method for optical characterization in Ch-LC.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Liquid Crystal Research Advancements · Surfactants and Colloidal Systems · Optical Polarization and Ellipsometry

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

References (33)

Show source-provided references
1. J. Grinberg, L.J. Miller, Circularly Polarized Light Source, U.S. PATENT DOCUMENTS, USA, 1978, p. 7.
2. Dierking · 2004
3. Scharf · 2007
4. Ely · Quim. Nova · 2007 · 30 · 177610.1590/S0100-40422007000700049 ↗
5. Christie · Color. Technol. · 2005 · 121 · 18710.1111/j.1478-4408.2005.tb00271.x ↗
6. Wang · Appl. Phys. Lett. · 2011 · 99 · 04110810.1063/1.3615293 ↗
7. Bobrovsky · Adv. Mater. · 2012 · 24 · 621610.1002/adma.201202227 ↗
8. Chen · RSC Adv. · 2014 · 4 · 5280410.1039/C4RA05787B ↗
9. Chen · J. Mater. Chem. C · 2014 · 2 · 438810.1039/c4tc00128a ↗
10. Hikmet · Adv. Mater. · 2002 · 14 · 50210.1002/1521-4095(20020404)14:7<502::AID-ADMA502>3.0.CO;2-G ↗
11. Dyer · Chem. Mater. · 1997 · 9 · 166510.1021/cm970070d ↗
12. Lin · J. Appl. Phys. · 2005 · 98 · 04311210.1063/1.2037191 ↗
13. Deng-Ke · J. Display Technol. · 2006 · 2 · 3210.1109/JDT.2005.861595 ↗
14. Geng · Appl. Phys. Lett. · 2006 · 89 · 08113010.1063/1.2339026 ↗
15. Broer · Nature · 1995 · 378 · 46710.1038/378467a0 ↗
16. Hikmet · Nature · 1998 · 392 · 47610.1038/33110 ↗
17. Raynes · Anal. Methods · 2009 · 1 · 8810.1039/b9ay00126c ↗
18. Araoka · J. Appl. Phys. · 2003 · 94 · 27910.1063/1.1578534 ↗
19. Park · Opt. Express · 2009 · 17 · 1232310.1364/OE.17.012323 ↗
20. Mitov · Nat. Mater. · 2006 · 5 · 36110.1038/nmat1619 ↗
21. Mitov · Liq. Cryst. · 2007 · 34 · 18310.1080/02678290601116175 ↗
22. Rusig · J. Polym. Sci., Part B: Polym. Phys. · 1994 · 32 · 190710.1002/polb.1994.090321108 ↗
23. Shirvani-Mahdavi · Opt. Express · 2010 · 18 · 502110.1364/OE.18.005021 ↗
24. Verbiest · J. Opt. Soc. Am. B: Opt. Phys. · 1998 · 15 · 45110.1364/JOSAB.15.000451 ↗
25. Alliprandini-Filho · J. Nanosci. Nanotechnol. · 2009 · 9 · 598110.1166/jnn.2009.1293 ↗
26. Collet · 1993
27. Therézio · J. Polym. Sci., Part B: Polym. Phys. · 2011 · 49 · 20610.1002/polb.22180 ↗
28. Therézio · J. Phys. Chem. C · 2013 · 117 · 1317310.1021/jp400823d ↗
29. Alliprandini Filho · Phys. Chem. Chem. Phys. · 2014 · 16 · 289210.1039/c3cp53803f ↗
30. Gennes · 1973
31. Alliprandini-Filho · Chem. Phys. Lett. · 2009 · 469 · 9410.1016/j.cplett.2008.12.057 ↗
32. Bobrovsky · Adv. Mater. · 2003 · 15 · 28210.1002/adma.200390067 ↗