Glass transition and α-relaxation dynamics of thin films of labeled polystyrene

Rodney D. Priestley, Linda J. Broadbelt, John M. Torkelson, and Koji Fukao
Phys. Rev. E 75, 061806 – Published 29 June 2007

Abstract

The glass transition temperature and relaxation dynamics of the segmental motions of thin films of polystyrene labeled with a dye, 4-[N-ethyl-N-(hydroxyethyl)]amino-4-nitroazobenzene (Disperse Red 1, DR1) are investigated using dielectric measurements. The dielectric relaxation strength of the DR1-labeled polystyrene is approximately 65 times larger than that of the unlabeled polystyrene above the glass transition, while there is almost no difference between them below the glass transition. The glass transition temperature of the DR1-labeled polystyrene can be determined as a crossover temperature at which the temperature coefficient of the electric capacitance changes from the value of the glassy state to that of the liquid state. The glass transition temperature of the DR1-labeled polystyrene decreases with decreasing film thickness in a reasonably similar manner to that of the unlabeled polystyrene thin films. The dielectric relaxation spectrum of the DR1-labeled polystyrene is also investigated. As the thickness decreases, the α-relaxation time becomes smaller, and the distribution of the α-relaxation times becomes broader. These results show that thin films of DR1-labeled polystyrene are a suitable system for investigating confinement effects of the glass transition dynamics using dielectric relaxation spectroscopy.

  • Figure
  • Figure
  • Figure
  • Figure
  • Figure
  • Figure
  • Figure
4 More
  • Received 13 December 2006

DOI:https://doi.org/10.1103/PhysRevE.75.061806

©2007 American Physical Society

Authors & Affiliations

Rodney D. Priestley1, Linda J. Broadbelt1, John M. Torkelson1,2,*, and Koji Fukao3,†

  • 1Department of Chemical and Biological Engineering, Northwestern University, Evanston, Illinois 60208-3120, USA
  • 2Department of Materials Science and Engineering, Northwestern University, Evanston, Illinois 60208-3120, USA
  • 3Department of Macromolecular Science and Engineering, Kyoto Institute of Technology, Matsugasaki, Kyoto 606-8585, Japan

  • *Corresponding author: j-torkelson@northwestern.edu
  • Corresponding author: kfukao@se.ritsumei.ac.jp Present address: Department of Physics, Ritsumeikan University, Kusatsu, Shiga, 525–8577 Japan.

Article Text (Subscription Required)

Click to Expand

References (Subscription Required)

Click to Expand
Issue

Vol. 75, Iss. 6 — June 2007

Reuse & Permissions
Access Options
Author publication services for translation and copyediting assistance advertisement

Authorization Required


×
×

Images

×

Sign up to receive regular email alerts from Physical Review E

Log In

Cancel
×

Search


Article Lookup

Paste a citation or DOI

Enter a citation
×