Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Letter
  • Published:

Residual stresses in thin polymer films cause rupture and dominate early stages of dewetting

Abstract

In attempting to reduce the size of functional devices, the thickness of polymer films has reached values even smaller than the diameter of the unperturbed molecule. However, despite enormous efforts for more than a decade1, our understanding of the origin of some puzzling properties of such thin films is still not satisfactory and several peculiar observations remain mysterious. For example, under certain conditions, such films show negative expansion coefficients2,3,4,5,6 or show undesirable rupture although energetically they are expected to be stable7. Here, we demonstrate that many of these extraordinary effects can be related to residual stresses within the film, resulting from the preparation of these films from solution by fast evaporation of the solvent8. Consequently, depending on thermal history and ageing time, such films show significant changes even in the glassy state9,10, which we quantify by dewetting experiments and corresponding theoretical studies. Identifying the relevance of frozen-in polymer conformations gives us a handle for manipulating and controlling properties of nanometric thin polymer films.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1: Influence of ageing on the probability for film rupture, expressed by means of the areal density of holes.
Figure 2: The shape of the rim during early stages of dewetting of thin polymer films on non-adsorbing substrates.
Figure 3: Typical results for dewetting of PS thin films on a non-adsorbing substrate.
Figure 4: The influence on dewetting of storing (ageing) PS films for increasing times below the glass-transition temperature.

Similar content being viewed by others

References

  1. Reiter, G. & Forrest, J. Properties of thin polymer films. Eur. Phys. J. E 8 (special issue), 101 (2002).

    Article  CAS  Google Scholar 

  2. Orts, W. J., van Zanten, J. H., Wu, W. -L. & Satija, S. K. Observation of temperature dependent thicknesses in ultrathin polystyrene films on silicon. Phys. Rev. Lett. 71, 867–870 (1993).

    Article  Google Scholar 

  3. Mukherjee, M. et al. Reversible negative thermal expansion of polymer. Phys. Rev. E 66, 061801 (2002).

    Article  Google Scholar 

  4. Kanaya, T. et al. Annealing effects on thickness of polystyrene thin films as studied by neutron reflectivity. Polymer 44, 3769–3773 (2003).

    Article  Google Scholar 

  5. Miyazaki, T., Nishida, K. & Kanaya, T. Contraction and reexpansion of polymer thin films. Phys. Rev. E 69, 022801 (2004).

    Article  Google Scholar 

  6. Richardson, H., Carelli, C., Keddie, J. L. & Sferrazza, M. Structural relaxation of spin-cast glassy polymer thin films as a possible factor in dewetting. Eur. Phys. J. E 12, 437–441 (2003).

    Article  Google Scholar 

  7. Bollinne, C., Cuenot, S., Nysten, B. & Jonas, A. M. Spinodal-like dewetting of thermodynamically-stable thin polymer films. Eur. Phys. J. E 12, 389–396 (2003).

    Article  Google Scholar 

  8. Reiter, G. & de Gennes, P. -G. Spin-cast, thin, glassy polymer films: Highly metastable forms of matter. Eur. Phys. J. E 6, 25–28 (2001).

    Article  Google Scholar 

  9. Priestley, R. D., Broadbelt, L. J. & Torkelson, J. M. Physical aging of ultrathin polymer films above and below the bulk glass transition temperature: Effects of attractive vs neutral polymer-substrate interactions measured by fluorescence. Macromolecules 38, 654–657 (2005).

    Article  Google Scholar 

  10. Kawana, S. & Jones, R. A. L. Effect of physical ageing in thin glassy polymer films. Eur. Phys. J. E 10, 223–230 (2003).

    Article  Google Scholar 

  11. Reiter, G. Dewetting of highly elastic thin polymer films. Phys. Rev. Lett. 87, 186101 (2001).

    Article  Google Scholar 

  12. Damman, P., Baudelet, N. & Reiter, G. Dewetting near the glass transition: Transition from a capillary force dominated to a dissipation dominated regime. Phys. Rev. Lett. 91, 216101 (2003).

    Article  Google Scholar 

  13. Redon, C., Brochard-Wyart, F. & Rondelez, F. Dynamics of dewetting. Phys. Rev. Lett. 66, 715–718 (1991).

    Article  Google Scholar 

  14. Brochard-Wyart, F., Martin, P. & Redon, C. Liquid/liquid dewetting. Langmuir 9, 3682–3690 (1993).

    Article  Google Scholar 

  15. Brochard-Wyart, F., Debrégeas, G., Fondecave, R. & Martin, P. Dewetting of supported viscoelastic polymer films: Birth of rims. Macromolecules 30, 1211–1213 (1997).

    Article  Google Scholar 

  16. Debrégeas, G., de Gennes, P. -G. & Brochard-Wyart, F. The life and death of “bare” viscous bubbles. Science 279, 1704–1707 (1998).

    Article  Google Scholar 

  17. Brenner, M. P. & Gueyffier, D. On the bursting of viscous films. Phys. Fluids 11, 737–739 (1999).

    Article  Google Scholar 

  18. Reiter, G. & Khanna, R. Real-time determination of the slippage length in autophobic polymer dewetting. Phys. Rev. Lett. 85, 2753–2756 (2000). Kinetics of autophobic dewetting of polymer films. Langmuir 16, 6351–6357 (2000).

    Article  Google Scholar 

  19. Dalnoki-Veress, K., Nickel, B. G., Roth, C. & Dutcher, J. R. Hole formation and growth in freely standing polystyrene films. Phys. Rev. E 59, 2153–2156 (1999).

    Article  Google Scholar 

  20. Saulnier, F., Raphäel, E. & de Gennes, P. -G. Dewetting of thin polymer films near the glass transition. Phys. Rev. Lett. 88, 196101 (2002). Dewetting of thin-film polymers. Phys. Rev. E 66, 061607 (2002).

    Article  Google Scholar 

  21. Shenoy, V. & Sharma, A. Dewetting of glassy polymer films. Phys. Rev. Lett. 88, 236101 (2002).

    Article  Google Scholar 

  22. Vilmin, T. & Raphäel, E. Dewetting of thin viscoelastic polymer films on slippery substrates. http://arxiv.org/abs/cond-mat/0502228 (2005).

  23. De Gennes, P. -G. Scaling Concepts in Polymer Physics 2nd edn (Cornell Univ. Press, Ithaca, New York, 1985).

    Google Scholar 

  24. Sivaniah, E., Sferrazza, M., Jones, R. A. L. & Bucknall, D. G. Chain confinement effects on interdiffusion in polymer multilayers. Phys. Rev. E 59, 885–888 (1999).

    Article  Google Scholar 

  25. Bucknall, D. G., Butler, S. A. & Higgins, J. S. Real-time measurement of polymer diffusion coefficients using neutron reflection. Macromolecules 32, 5453–5456 (1999).

    Article  Google Scholar 

Download references

Acknowledgements

This work was supported by the Belgian National Fund for Scientific Research (FNRS), the Research Ministry of the Walloon Region and the Social European Fund. Pascal Damman is a Research Associate of the FNRS. Both teams from France acknowledge financial support from the European Community’s ‘Marie-Curie Actions’ under contract MRTN-CT-2004-504052 [POLYFILM].

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Günter Reiter.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Reiter, G., Hamieh, M., Damman, P. et al. Residual stresses in thin polymer films cause rupture and dominate early stages of dewetting. Nature Mater 4, 754–758 (2005). https://doi.org/10.1038/nmat1484

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/nmat1484

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing