Particle Dynamics in a Diblock-Copolymer-Based Dodecagonal Quasicrystal and Its Periodic Approximant by X-Ray Photon
Andreas J Mueller1, Aaron P Lindsay1, Ronald M Lewis2
1Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, Minnesota 55455, USA.
X-ray photon correlation spectroscopy (XPCS) revealed faster structural dynamics in dodecagonal quasicrystals compared to σ phase approximants. These findings in block copolymer blends offer new insights into soft material dynamics.
Area of Science:
- Soft matter physics
- Polymer science
- Materials science
Background:
- Block copolymer blends can self-assemble into complex ordered structures.
- Understanding the dynamics of these structures is crucial for material applications.
- Quasicrystals and approximants represent unique self-assembled phases.
Purpose of the Study:
- To investigate the temperature-dependent dynamics of a binary diblock-copolymer blend.
- To compare the structural relaxation dynamics between a dodecagonal quasicrystal and a Frank-Kasper σ phase.
- To elucidate the origins of observed dynamical differences.
Main Methods:
- Utilized temperature-dependent x-ray photon correlation spectroscopy (XPCS).
- Analyzed Bragg scattering from self-assembled diblock-copolymer structures.
- Measured structural relaxation times as a function of wavevector and temperature.
Main Results:
- Structural relaxation times were independent of the Bragg scattering wavevector.
- Dynamics were approximately 5 times faster in the dodecagonal quasicrystal phase compared to the σ phase.
- Minimal temperature dependence was observed for the relaxation times in both phases.
Conclusions:
- Dynamical relaxations are attributed to particle motion at grain boundaries in these tetrahedrally close-packed assemblies.
- XPCS successfully measured unprecedented particle dynamics in ordered soft materials.
- This work expands the utility of XPCS for studying dynamics in complex soft matter systems.
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