Hostname: page-component-586b7cd67f-2plfb Total loading time: 0 Render date: 2024-11-28T06:36:57.111Z Has data issue: false hasContentIssue false

Surface Modification of ZrO2 Nanoparticles as Functional Component in Optical Nanocomposite Devices

Published online by Cambridge University Press:  01 February 2011

Ninjbadgar Tsedev
Affiliation:
[email protected], Max Planck Institute of Colloids and Interfaces, Dept. of Colloid Chemistry, Research Campus Golm, Potsdam, 14424, Germany
Georg Garnweitner
Affiliation:
[email protected], TU Braunschweig, Institute of Particle Technology, Volkmaroder Str. 5, Braunschweig, 38104, Germany, +495313919615, +495313919633
Get access

Abstract

We have recently shown the successful synthesis of zirconia nanoparticles that can be optimized for use in volume phase holography by a post-functionalization surface treatment. Here, we present further investigations on the surface modification treatment with the aim of providing tools to tailor the nanoparticle compatibility to the photocurable organic matrix. Highly crystalline ZrO2 nanoparticles with a mean diameter of 5nm are synthesized in multigram yield through a one-pot solvothermal reaction of zirconium (IV) n-propoxide in benzyl alcohol. It is shown that the yield of the ZrO2 nanoparticles and stability of the nanoparticle dispersions are strongly dependent on the synthesis temperature. Post-synthetic surface modification of ZrO2 nanoparticles using several aliphatic ligands with different surface binding groups such as carboxylate (-COO), amine (−NH2), phosphate (−PO4) and methoxysilane (−SiOCH3) was performed in order to compare the binding ability of these functional groups to the nanoparticle surface and therefore provide a new rational approach for nanoparticle stabilization with organic ligands.

Type
Research Article
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

1. Matharu, A.S. Jeeva, S. and Ramanujam, P.S. Chem. Soc. Rev. 36, 1868 (2007).Google Scholar
2. Gu, C. Xu, Y. Liu, Y. Pan, J.J. Zhou, F. He, H. Optical Mater. 23, 219 (2003).Google Scholar
3. Barachevskii, V.A. High Energy Chem. 40, 165 (2006).Google Scholar
4. Sánchez, C., Escuti, M.J. Heesch, C. van, Bastiaansen, C.W.M., Broer, D.J. Loos, J. and Nussbaumer, R., Adv. Funct. Mater. 15, 1623 (2005).Google Scholar
5. Sakhno, O.V. Smirnova, T.N. Goldenberg, L.M. and J.Stumpe, Mater. Sci. and Eng. C, 28, 28 (2008).Google Scholar
6. Garnweitner, G. Goldenberg, L.M. Sakhno, O.V. Antonietti, M. Niederberger, M. and Stumpe, J., Small, 3,1626(2007).Google Scholar
7. Saravanamuttu, K. Blanford, C.F. Sharp, D.N. Dedman, E.R. Turberfield, A.J. and Denning, R.G., Chem. Mater. 15, 2301 (2003).Google Scholar
8. Suzuki, N. Tomita, Y. and Kojima, T. Appl. Phys. Lett. 81, 4121 (2002).Google Scholar
9. Zhou, S. Garnweitner, G. Niederberger, M. Antonietti, M. Langmuir 23, 9178 (2007).Google Scholar
10. Yee, C.K. Ulman, A. Ruiz, J.D. Parikh, A. White, H. and Rafailovich, M. Langmuir, 19, 9450 (2003).Google Scholar
11. Hostetler, M.J. Stokes, J.J. and Murray, R.W. Langmuir 12, 3604 (1996).Google Scholar
12. Palma, R. De, Peeters, S. Bael, M.J. van, Rul, H. van den, Bonroy, K. Laureyn, W. Mullens, J. Borghs, G. and Maes, G. Chem. Mater. 19, 1821 (2007).Google Scholar
13. Guerrero, G. Mutin, P.H. and Vioux, A. Chem. Mater. 13, 4367 (2001).Google Scholar