Synthesis and Characterization of a New Photoconducting Poly(siloxane) Having Pendant Diphenylhydrazone for Photorefractive Applications

  • Lee, Sang-Ho (Optoelectronic Materials Research Center, Korea Institute of Science and Technology) ;
  • Jahng, Woong-Sang (Optoelectronic Materials Research Center, Korea Institute of Science and Technology) ;
  • Park, Ki-Hong (Optoelectronic Materials Research Center, Korea Institute of Science and Technology) ;
  • Kim, Nakjoong (Department of Chemistry, Hanyang University) ;
  • Joo, Won-Jae (Department of Chemistry, Hanyang University) ;
  • Park, Dong-Hoon (College of Environment & Applied Chemistry, Kyunghee University)
  • Published : 2003.12.01

Abstract

A new photoconducting polymer, diphenyl hydrazone-substituted polysiloxane, was successfully synthesized by the hydrosilylation method and characterized by FT-IR, $^1$H-NMR, and $^{29}$ Si-NMR spectroscopy. The glass transition temperature (T$_{g}$) of the polysiloxane having pendant diphenyl hydrazone was ca. 62 $^{\circ}C$, which enabled a component of a low-T$_{g}$ photorefractive material to be prepared without the addition of any plasticizers. This polysiloxane, with 1 wt% of $C_{60}$ dopant, showed a high photoconductivity (2.8 ${\times}$ 10$^{-12}$ S/cm at 70 V/${\mu}{\textrm}{m}$) at 633 nm, which is necessary for fast build-up of the space-charge field. A photorefractive composite was prepared by adding a nonlinear optical chromophore, 2-{3-[2-(dibutylamino)-1-ethenyl]-5,5-dimethyl-2-cyclohexenylidene} malononitrile, into the photoconducting polysiloxane together with $C_{60}$ . This composite shows a large orientation birefringence ($\Delta$n = 2.6 ${\times}$ 10$^{-3}$ at 50 V/${\mu}{\textrm}{m}$) and a high diffraction efficiency of 81 % at an electric field of 40 V /${\mu}{\textrm}{m}$.textrm}{m}$.EX>.

Keywords

References

  1. J. Appl. Phys. v.38 A.Ashkin;G.D.Boyd;J.M.Dziedzic;R.G.Smith;A.A.Ballman;Levinstein;K.Nassau https://doi.org/10.1063/1.1710138
  2. Chem. Rev. v.94 W.E.Morner;S.M.Silence https://doi.org/10.1021/cr00025a005
  3. Appl. Phys. Lett. v.72 E.Hendrickx;J.Herlocker;J.L.Maldonaldo;S.R.Marder;B.Kippelen;A.Persoons;N.Peyghambarian https://doi.org/10.1063/1.121187
  4. Nature v.371 K.Meerholtz;B.L.Volodin;Sandalphon;B.Kippelen;N.Peyghambarian https://doi.org/10.1038/371497a0
  5. J. Opt. Soc. Am. B v.15 S.Schloter;U.Hofmann;P.Strohriegl;H.W.Schmidt;D.J.Haarer https://doi.org/10.1364/JOSAB.15.002473
  6. Appl. Phys. Lett. v.72 E.Hendrickx;J.Herlocker;J.L.Maldonaldo;S.R.Marder;B.Kippelen;A.Persoons;N.Peyghambarian https://doi.org/10.1063/1.121187
  7. Appl. Phys. Lett. v.74 J.A.Herlocker;K.B.Ferrio;E.Hendrickx;B.D.Guenther;S.Mery;B.Kippelen;N.Peyghambarian https://doi.org/10.1063/1.123816
  8. Chem. Mater. v.11 M.A.Diaz-Garcia;D.Wright;D.Casperson;B.Smith;E.Glazer;W.E.Moerner;L.I.Sukhomlinova;R.J.Twieg https://doi.org/10.1021/cm981157h
  9. Bull. Kor. Chem. Soc. v.23 N.J.Kim;H.Chun;K.K.Moon;W.J.Joo;N.Kim https://doi.org/10.5012/bkcs.2002.23.4.571
  10. Appl. Phys. Lett. v.70 A.Grunnet-Jespen;C.L.Thompson;R.J.Twieg;W.E.Moerner
  11. J.Phys. Chem. B v.103 T.Sasaki;M.Goto;Y.Ishikawa;T.Yoshimi https://doi.org/10.1021/jp983661f
  12. J. Appl. Phys. v.60 L.B.Schein;A.Rosenberg;S.L.Rice https://doi.org/10.1063/1.337471
  13. Science v.263 M.Liphardt;A.Goonesekera;B.E.Jones;S.Ducharme;J.M.Takacs;L.Zhang https://doi.org/10.1126/science.263.5145.367
  14. Adv. Mater. v.11 R.Bittner;T.K.Daubler;D.Neher;K.Meerholz https://doi.org/10.1002/(SICI)1521-4095(199902)11:2<123::AID-ADMA123>3.0.CO;2-R
  15. Chem. Mater. v.13 H.Chun;I.K.Moon;D.H.Shin;N.Kim https://doi.org/10.1021/cm000913s
  16. Teh Chemistry of Organic Silicon Compounds S.Patai;Z.Rappoport
  17. NMR-17 Oxygen-17 and Silicon-29 P.Diehl;E.Fluck;R.Kosfeld
  18. Chem. Rev. v.94 W.E.Moerner;S.M.Silence https://doi.org/10.1021/cr00025a005
  19. Synthetic Metals v.129 H.Chun;N.J.Kim;W.J.Joo;J.W.Han;C.H.Oh;N.Kim https://doi.org/10.1016/S0379-6779(02)00083-8
  20. Appl. Phys. Lett. v.74 K.Ogino;S.H.Park;H.Sato https://doi.org/10.1063/1.124229
  21. J. Mater. Chem. v.12 H.Chun;I.K.Moon;D.H>Shin;S.Song;N.Kim https://doi.org/10.1039/b105555k