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Orientational order and finite strain in nematic elastomers
1Department of Mechanical and Aerospace Engineering, Washington University in St. Louis, 1 Brookings Drive, Box 1185, St. Louis, Missouri 63130-4899, USA. efried@me.wustl.edu
The Journal of Chemical Physics
|August 13, 2005
Summary
Nematic elastomers show significant shape changes during phase transitions. A new theory explains these deformations by linking polymer elasticity and molecular order, influencing transition temperatures.
Area of Science:
- Materials Science
- Polymer Physics
- Soft Matter Physics
Background:
- Nematic elastomers undergo substantial spontaneous shape changes when transitioning from an isotropic to a nematic phase.
- Understanding these large deformations is crucial for developing advanced materials with tunable properties.
Purpose of the Study:
- To develop a nonlinear, variational theory for nematic elastomers that couples orientational order and elastic deformation.
- To investigate how elastic properties influence the isotropic-nematic transition temperature and the resulting spontaneous shape changes.
Main Methods:
- Formulation of a free-energy functional comprising nematic and elastic contributions.
- Minimization of the free-energy functional to model finite deformations and phase transitions.
- Analysis of the interplay between mesogenic unit interactions and polymer chain stretching.
Main Results:
- The developed theory accurately describes large, reversible, spontaneous shape changes in nematic elastomers.
- Elastic deformation was shown to significantly impact the isotropic-nematic transition temperature.
- The magnitude of spontaneous deformation was quantified for various material parameters.
Conclusions:
- The theory provides a robust framework for understanding and predicting the behavior of nematic elastomers.
- This work offers insights into designing materials with controlled shape-changing capabilities.
- The model encompasses soft elasticity as a specific instance but is broadly applicable.