Hostname: page-component-848d4c4894-nr4z6 Total loading time: 0 Render date: 2024-05-26T19:30:38.922Z Has data issue: false hasContentIssue false

Optical properties of organic-dye-doped spherical particles of polyorganosiloxane derived from methyltrimethoxysilane using a reaction field of W/O emulsion

Published online by Cambridge University Press:  31 January 2011

Taichi Matsumoto
Affiliation:
Department of Applied Chemistry, Faculty of Science and Engineering, Ritsumeikan University, Kusatsu, Shiga 525-8577, Japan
Masahiro Miki
Affiliation:
Department of Applied Chemistry, Faculty of Science and Engineering, Ritsumeikan University, Kusatsu, Shiga 525-8577, Japan
Kazuo Kojima*
Affiliation:
Department of Applied Chemistry, Faculty of Science and Engineering, Ritsumeikan University, Kusatsu, Shiga 525-8577, Japan
Noriyuki Wada
Affiliation:
Department of Materials Science and Engineering, Suzuka National College of Technology, Siroko, Suzuka, Mie 510-0294, Japan
*
a)Address all correspondence to this author. e-mail: kojimaka@se.ritsumei.ac.jp
Get access

Abstract

Polyorganosiloxane spherical particles were synthesized by a sol-gel method from methyltrimethoxysilane (MTMS) using a reaction field of W/O emulsion consisting of sorbitantrioleate (SPAN85), n-octane, and aqueous solutions of basic, acid, and oil-soluble organic dyes. The investigation focused on the types of dyes suitable for incorporation into the spherical particles by using this method. The morphology of the particles was observed with scanning electron microscopy (SEM). Fluorescence and ultraviolet-visible (UV-vis) reflectance spectra of dye-doped spherical particles were measured. Basic dyes [Rhodamine B (RB), Rhodamine 6G (R6G), Crystal Violet (CV), Malachite Green (MG), and Thioflavin T (TT)] were doped into the spherical particles. Spherical particles obtained from aqueous solutions of RB, R6G, and CV were colored deeply. However, the MG- and TT-doped particles were scarcely colored. The reason for this color difference was discussed based on the comparison of UV-vis reflectance spectra of dye-doped spherical particles with absorption spectra of starting solutions of the dyes. It is found that the dye that tends to form dimers in aqueous solution was doped more easily than the dyes that tend to form monomers only. On the other hand, spherical particles obtained from acid dyes [Fluorescein Sodium Salt (FSS), Orange G (OG), Naphthol Green B (NGB), and Erythrosin B (EB)] and oil-soluble dye [Fluorescein (FLU)] were all white, confirming that these dyes were not doped in the particles. The reason was discussed in terms of the nature of the dyes and the formation mechanism of the spherical particles.

Type
Articles
Copyright
Copyright © Materials Research Society 2008

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

1Avnir, D., Levy, D.Reisfeld, R.: The nature of the silica cage as reflected by spectral changes and enhanced photostability of trapped rhodamine 6G. J. Phys. Chem. 88, 5956 1984Google Scholar
2Avnir, D., Kaufman, V.R.Reisfeld, R.: Organic fluorescent dyes trapped in silica and silica-titania thin films by the sol-gel method. Photophysical, film and cage properties. J. Non-Cryst. Solids 74, 395 1985Google Scholar
3Negishi, N., Mutsuko, F., Yamashita, H., Fox, M.A.Anpo, M.: Photophysical properties and photochemical stability of rhodamine B encapsulated in SiO2 and Si–Ti binary oxide matrices by the sol-gel method. Langmuir 10, 1772 1994Google Scholar
4Nobuaki, N., Yamashita, H.Anpo, M.: The characteristics of fluorescence spectra of rhodamine B molecules doped in Si–Ti binary oxide system by the sol-gel method. Chem. Lett. (Jpn.) 6, 1029 1994Google Scholar
5Fujii, T.Ishii, A.: Absorption and fluorescence spectra of rhodamine B molecules encapsulated in silica gel networks and their thermal stabitily. J. Photochem. Photobiol. A 54, 231 1990Google Scholar
6Qian, G.Wang, M.: Study on the microstructural evolution of silica gel during sol-gel-gel-glass conversions using the fluorescence polarization of rhodamine B. J. Phys. D: Appl. Phys. 32, 2462 1999Google Scholar
7Takahashi, Y., Yamanaka, T.Uchida, K.: Time-resolved fluorescence spectra and energy migration of rhodamine B doped in amorphous silica glasses. J. Lumin. 62, 299 1994Google Scholar
8Severin-Vantilt, M.M.E.Oomen, E.W.J.L.: The incorporation of rhodamine B in silica sol-gel layers. J. Non-Cryst. Solids 159, 38 1993Google Scholar
9Kobayashi, Y., Kurokawa, Y.Imai, Y.: A transparent alumina film doped with laser dye and its emission properties. J. Non-Cryst. Solids 105, 198 1988CrossRefGoogle Scholar
10Zhu, X.L., Lam, S.K., Chan, M.A., Tsang, Y.Lo, D.: Recent development of organic dye-doped sol-gel materials for photonics in Sol-Gel Optics V,, edited by B.S. Dunn, E.J.A. Pope, H.K. Schmidt, and M. Yamanein (Proceedings of SPIE , 2000) Vol. 3943, p. 210Google Scholar
11Lam, S.K.Lo, D.: Time-resolved spectroscopic study of phosphorescence and delayed fluorescence of dyes in silica-gel glasses. Chem. Phys. Lett. 281, 35 1997Google Scholar
12Suratwala, T., Gardlund, Z., Davidson, K.Uhlmann, D.R.: Silylated coumarin dyes in sol-gel hosts. 2. Photostability and sol-gel processing. Chem. Mater. 10, 199 1998Google Scholar
13Shibata, S., Miyake, M., Kamada, K., Ohta, K., Sasaki, K.Masuhara, H.: Laser emission from dye-doped organic-inorganic particles of microcavity structure. J. Sol.-Gel Sci. Technol. 8, 959 1997Google Scholar
14Brunel, M., Luyer, F.L., Canva, M., Burn, A., Chaput, F., Malier, L.Boilot, J-P.: Reverse-saturable absorption in aluminophthalcyanine-doped xerogels. Appl. Phys. B 58, 443 1994Google Scholar
15Boilot, J-P., Biteau, J., Chaput, F., Gacoin, T., Brun, A., Darracq, B., Georges, P.Levy, Y.: Organic–inorganic solids by sol-gel processing: Optical applications. Pure Appl. Opt. 7, 169 1998Google Scholar
16Anedda, A., Carbonaro, C.M., Corpino, R., Ricci, P.C., Grandi, S.Mustarelli, P.C.: Formation of fluorescent aggregates in Rhodamine 6G doped silica glasses. J. Non-Cryst. Solids 353, 481 2007Google Scholar
17Laranjo, M.T., Stefani, V., Benvenutti, E.V., Costa, T.M.H., de Ramminger, G. O.Gallas, M.R.: Synthesis of ORMOSIL silica/rhodamine 6G: Powders and compacts. J. Non-Cryst. Solids 353, 24 2007Google Scholar
18Anedda, A., Carbonaro, C.M., Clemente, F., Corpino, R., Grandi, S., Magistris, A.Mustarelli, P.C.: Rhomdamin 6G-SiO2 hybrids: A photoluminescence study. J. Non-Cryst. Solids 351, 1850 2005CrossRefGoogle Scholar
19Mahltig, B.Textor, T.: Combination of silica sol and dyes on textiles. J. Sol.-Gel Sci. Technol. 39, 111 2006Google Scholar
20Uricanu, V.I., Donescu, D., Banu, A.G., Serban, S., Vasilescu, M., Olteanu, M.Dudau, M.: Influence of film structure and precursor composition on rhodamine B retention in dye-dopped ormosils. J. Sol.-Gel Sci. Technol. 34, 23 2005Google Scholar
21Kuwata-Gonokami, M., Takeda, K., Yasuda, H.Ema, K.: Laser emission from dye-doped polystyrene microsphere. Jpn. J. Appl. Phys. 31, L99 1992CrossRefGoogle Scholar
22Sasaki, K.: Microspectoroscopy with an optically-manipulated lasing partcle. Mater. Sci. Eng., B 48, 147 1997Google Scholar
23Misawa, H., Fujisawa, R., Sasaki, K., Kitamura, N.Masuhara, H.: Simultaneous manipulation and lasing of a polymer microparticle using a CW 1064 nm laser beam. Jpn. J. Appl. Phys. 32, L788 1993CrossRefGoogle Scholar
24Chang, T.Cheung, H.C.: Solvent effects of the photomerization rates of the zwitterionic and the cationic forms of rhodamine B in protic solvent. J. Phys. Chem. 96, 4874 1992CrossRefGoogle Scholar
25Glaser, R.H.Wilks, G.L.: Solid-state 29Si NMR of TEOS-based multifunctional sol-gel materials. J. Non-Cryst. Solids 113, 73 1989Google Scholar
26Matsumoto, T., Takayama, Y., Wada, N., Onoda, H.Kojima, K.: Synthesis of rhodamine B-doped and monodispersed spherical particles of polyorganosiloxane using a W/O emulsion. J. Am. Ceram. Soc. 88, 3458 2005Google Scholar
27Matsumoto, T., Takayama, Y., Wada, N., Onoda, H., Kojima, K., Yamada, H.Wakabayashi, H.: Acid-free synthesis of poly-organo-siloxane spherical paricles using a W/O emulsion. J. Mater. Chem. 13, 1746 2003Google Scholar
28Bindhu, C.V., Harilal, S.S., Varier, G.K., Issac, R.C., Nampoori, V.P.N.Vallabhan, C.P.G.: Mesurement of the absolute fluorescence quantum yield of rhodamine B solution using a dual-beam thermal lens technique. J. Phys. D: Appl. Phys. 29, 1074 1996Google Scholar
29Rao, K.S., Prakash, G.V.Murthy, J.S.R.: Ultrasonic, dielectric and fluorescence spectral studies of dimerization effects in dilute aqueous solutions of laser dye rhodamine B. Indian J. Pure Appl. Phys. 36, 1 1998Google Scholar
30Schirra, R.: Dye aggregation in freezing aqueous solutions. Chem. Phys. Lett. 119, 463 1985CrossRefGoogle Scholar
31Lin, H-T., Bescher, E., Mackenzie, J.D., Dai, H.Stafsudd, O.M.: Preparation and properties of laser dye-ORMOSIL composites. J. Mater. Sci. 27, 5523 1992CrossRefGoogle Scholar
32Lueck, H.B., McHale, J.L.Edwards, W.D.: Symmetry-breaking solvent effects on the electronic structure and spectra of a series of triphenylmethan dyes. J. Am. Chem. Soc. 114, 2342 1992Google Scholar
33Clark, F.T.Drickamer, H.G.: The effect of pressure on the adsorption of crystal violet on oriented ZnO crystals. J. Chem. Phys. 81, 1024 1984CrossRefGoogle Scholar
34Clark, F.T.Drickamer, H.G.: High-pressure study of tripheylmetane dyes in polymeric and aqueous media. J. Phys. Chem. 90, 589 1986Google Scholar
35Garcia-Rio, L., Hervella, P., Mejuto, J.C.Parajo, M.: Spectroscopic and kinetic investigation of the interaction between crystal violet and sodium dodecylsulfate. Chem. Phys. 335, 164 2007Google Scholar
36Garcia-Rio, L., Godoy, A.Leis, J.R.: Spectroscopic characterisation of crystal violet inclusion complexes in β-cyclodextrin. Chem. Phys. Lett. 401, 302 2005Google Scholar
37Dimitrijevic, N.M., Takahashi, K.Jonah, C.D.: Visible absorption spectra of crystal violet in supercritical ethane-methanol solution. J. Supercrit. Fluids 24, 153 2002Google Scholar
38Stork, W.H.J., Lippits, G.J.M.Mandel, M.: Association of crystal violet in aqueous solutions. J. Phys. Chem. 76, 1772 1972CrossRefGoogle Scholar
39Lueck, H.B., Rice, B.L.Mchale, J.L.: Aggregation of triphenylmethane dyes in aqueous solution: Dimerization and trimerization of crystal violet and ethyl violet. Specrtochim. Acta, Part A 48, 819 1992CrossRefGoogle Scholar
40Yao, H., Inoue, Y., Ikeda, H., Nakatani, K., Kim, H-B.Kitamura, N.: Micrometer size effect on dye association in single laser-trapped water droplets. J. Phys. Chem. 100, 1494 1996CrossRefGoogle Scholar
41Muir, R.N.Alexander, A.J.: Structure of monolayer dye films studied by Brewster angle cavity ringdown spectroscopy. Phys. Chem. Chem. Phys. 5, 1279 2003CrossRefGoogle Scholar