journal article·2010-07

Second harmonic generation in SiO2 sol–gel films functionalized with Ethyl-[4-(4-nitro-phenylazo)-phenyl]-(2-oxiranylmethoxy-ethyl)-amine (ENPMA) molecules

Alfredo Franco, Giovanna Brusatin, Massimo Guglielmi, Glauco Stracci, Fabio De Matteis, Mauro Casalboni, Heiner Detert, Bernd Grimm, Sigurd Schrader

Journal of Non-Crystalline Solids· Volume 356· Issue 33-34
Publisher page

Abstract

Abstract High concentrations of Ethyl-[4-(4-nitro-phenylazo)-phenyl]-(2-oxiranylmethoxy-ethyl)-amine (ENPMA) chromophores were linked covalently to two different kinds of SiO 2 matrices prepared by the sol–gel method. The matrices differed in their reticulation level, determined by the organometallic precursor used during the synthesis. The materials were deposited as films by spin-coating. The chromophores in the films were oriented in a non-centrosymmetric way by a modified Corona poling set-up, and the nonresonant second order non-linear optical coefficient d 33 (0) of the films was determined by means of the Maker fringe technique. It was found that there is an optimum concentration of chromophores for attaining the highest d 33 (0) value in these materials. Their maximum d 33 (0) value was found in the films with the least reticulated matrix, that value was equal to 5.2 ± 0.5 pm/V. Besides, the d 33 (0) value was more stable in time in the less reticulated materials.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Nonlinear Optical Materials Research · Photochemistry and Electron Transfer Studies · Porphyrin and Phthalocyanine Chemistry

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

References (23)

Show source-provided references
1. Kim · Mol. Cryst. Liq. Cryst. · 2001 · 371 · 33710.1080/10587250108024755 ↗
2. Enami · Appl. Phys. Lett. · 2003 · 82 · 49010.1063/1.1539298 ↗
3. Enami · Nat. Photonics · 2007 · 1 · 18010.1038/nphoton.2007.25 ↗
4. Sullivan · J. Ligthwave Technol. · 2008 · 26 · 234510.1109/JLT.2008.927147 ↗
5. Cho · Prog. Polym. Sci. · 2008 · 33 · 101310.1016/j.progpolymsci.2008.07.007 ↗
6. Brusatin · J. Eur. Ceram. Soc. · 2004 · 24 · 185310.1016/S0955-2219(03)00601-0 ↗
7. Chaumel · Chem. Mater. · 2001 · 13 · 338910.1021/cm011017z ↗
8. Briers · Macromol. Rapid Commun. · 2007 · 28 · 94210.1002/marc.200700030 ↗
9. Lu · Macromolecules · 2004 · 37 · 7084
10. No · Bull. Korean Chem. Soc. · 2010 · 31 · 42910.5012/bkcs.2010.31.02.429 ↗
11. Aljoumaa · Macromolecules · 2009 · 42 · 927510.1021/ma900930q ↗
12. Li · Phys. Chem. Chem. Phys. · 2009 · 11 · 122010.1039/b816246h ↗
13. Xie · J. Phys.: Conf. Ser. · 2006 · 28 · 95
14. Jellison · Appl. Phys. Lett. · 1996 · 69 · 37110.1063/1.118064 ↗
15. Shoji · Opt. Quantum Electron. · 2002 · 34 · 79710.1023/A:1016545417478 ↗
16. Hayden · J. Appl. Phys. · 1990 · 68 · 45610.1063/1.346815 ↗
17. Jerphagnon · J. Appl. Phys. · 1970 · 41 · 166710.1063/1.1659090 ↗
18. Mortazavi · J. Opt. Soc. Am. B · 1989 · 6 · 73310.1364/JOSAB.6.000733 ↗
19. Page · J. Opt. Soc. Am. B · 1990 · 7 · 123910.1364/JOSAB.7.001239 ↗
20. Burland · Chem. Rev. · 1994 · 94 · 3110.1021/cr00025a002 ↗
21. McGrath · Polymer · 2006 · 47 · 404210.1016/j.polymer.2006.02.030 ↗
22. Kitaoka · Jpn. J. Appl. Phys. · 1999 · 38 · L102910.1143/JJAP.38.L1029 ↗
23. Reyes-Esqueda · Optics Comm. · 2001 · 198 · 20710.1016/S0030-4018(01)01498-5 ↗