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Current issue   Ukr. J. Phys. 2014, Vol. 58, N 5, p.480-489
https://doi.org/10.15407/ujpe58.05.0480    Paper

Petrenko V.Yu.1, Slominskii Yu.L.2, Smirnova G.L.2, Mazarchuk I.A.1, Dimitriev O.P.1

1 V.E. Lashkaryov Institute of Semiconductor Physics, Nat. Acad. of Sci. of Ukraine
(41, Nauky Ave., Kyiv 03028, Ukraine; e-mail: dimitr@isp.kiev.ua)
2 Institute of Organic Chemistry, Nat. Acad. of Sci. of Ukraine
(5, Murmanska Str., Kyiv 02660, Ukraine)

Influence of CdTe Nanoparticles on the Formation of J-Aggregates of Thiamonomethinecyanine Dyes

Section: Nanosystems
Original Author's Text: Ukrainian

Abstract: Conditions of J-aggregate formation have been studied for three types of thiamonomethinecyanine dyes, the structures of which differ from one another by their end groups, and the dependences of those conditions on the dye concentration and the type of dye interaction with CdTe nanoparticles with a diameter of 3 nm in aqueous dispersions have been analyzed. The dye structure is found to influence the efficiency of the J-aggregate formation in solutions and films. It is also found that CdTe quantum dots (QDs) stabilized by thioglycolic acid can adsorb J-aggregates of dye molecules on their surface. It is shown for the first time that the hybrid structure dye–CdTe can emerge owing to the interaction between the negatively charged dye molecules and the negatively charged surface of QDs forming neutral aggregates. No process of energy transfer from the dye to a CdTe particle was detected in the dimer–CdTe and J-aggregate–CdTe systems.

Key words: thiamonomethinecyanine, thioglycolic acid, polymethine, pseudoisocyanine, floccules, peptization, redispersion, F¨orster mechanism.


  1. A.I. Tolmachev, Yu.L. Slominskii, and A.A. Ishchenko, in Near-Infrared Dyes for High Technology Applications, edited by S. Daehne, U. Resch-Genger, and O.S. Wolfbeis (Kluwer, Dordrecht, 1998), p. 385. https://doi.org/10.1007/978-94-011-5102-3_19
  2. N.A. Davidenko, A.A. Ishchenko, and N.G. Kuvshinskii, Photonics of Molecular Semiconductor Composites Based on Organic Dyes (Naukova Dumka, Kyiv, 2005) (in Russian).
  3. A.A. Ishchenko, in Specialty Polymers. Materials and Applications, edited by F. Mohammad (I.K. Intern. Publ. House, New Delhi, 2007), p. 301.
  4. B.H. Soffer and B.B. McFarland, Appl. Phys. Lett. 10, 266 (1967). https://doi.org/10.1063/1.1754804
  5. P.P. Sorokin and J.R. Lankard, IBM J. Res. Develop. 10, 162 (1966). https://doi.org/10.1147/rd.102.0162
  6. Dye Lasers, edited by F.P. Sch¨affer (Springer, New York, 1973).
  7. I.I. Filimonova, S.L. Yefimova, and A.V. Sorokin, Funct. Mater. 19, 348 (2012).
  8. G.Ya. Guralchuk, I.K. Katrunov, R.S. Grynyov, A.V. Sorokin, S.L. Efimova, I.A. Borovoy, and Y.V. Malyukin, J. Phys. Chem. C 112, 14762 (2008). https://doi.org/10.1021/jp802933n
  9. A.V. Sorokin, B.A. Gnap, I.I. Filimonova, and S.L. Yefimova, Funct. Mater. 19, 70 (2012).
  10. M.G. Reva, L.V. Levshin, and B.D. Ryzhikov, Zh. Prikl. Spektrosk. 33, 668 (1980).
  11. A.K. Chibisov, Khim. Vysok. Energ. 41, 239 (2007).
  12. P.S. Grinev, A.V. Sorokin, G.Ya. Guralchuk, S.L. Yefimova, I.A. Borovoy, and Yu.V. Malyukin, Biofiz. Visn. 21, 101 (2008).
  13. A. Dixon, C. Duncan, and H. Samha, Am. J. Undergrad. Res. 3, No. 4, 29 (2005).
  14. J.E. Halpert, J.R. Tisher, G. Nair, B.J. Walker, W. Liu, V. Bulovik, and M.G. Bavendi, J. Phys. Chem. C 113, 9986 (2009). https://doi.org/10.1021/jp8099169
  15. M.V. Kovalenko, M I. Bodnarcyuk, A.L. Strouk, and S.Ya. Kuchmii, Theor. Exper. Chem. 40, 220 (2004). https://doi.org/10.1023/B:THEC.0000041806.60632.04
  16. W.W. Yu, L. Qu, W. Guo, and X. Peng, Chem. Mater.15, 2854 (2003). https://doi.org/10.1021/cm034081k
  17. F.M. Hamer, The Cyanine Dyes and Related Compounds (Interscience, New York, 1964).
  18. V.M. Agranovich, Yu.N. Gartstein, and M. Litinskaya, Chem. Rev. 111, 5179 (2011). https://doi.org/10.1021/cr100156x
  19. B.M. Smirnov, Usp. Fiz. Nauk 161, No. 6, 171 (1991). https://doi.org/10.3367/UFNr.0161.199106e.0171