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Dynamically asymmetric binary glass formers studied by dielectric and NMR spectroscopy
Th Körber1, R Minikejew1, B Pötzschner1
1Universität Bayreuth, Anorganische Chemie III and Nordbayerisches NMR-Zentrum, D-95440, Bayreuth, Germany.
The European Physical Journal. E, Soft Matter
|November 28, 2019
Summary
Investigating asymmetric binary glass formers, this study reveals that component dynamics change with concentration. A generalized function describes spectra, showing dynamic heterogeneities in the low-Tg component.
Area of Science:
- Materials Science
- Physical Chemistry
- Condensed Matter Physics
Background:
- Binary glass formers exhibit complex dynamics influenced by component interactions.
- Understanding component dynamics is crucial for designing materials with specific properties.
Purpose of the Study:
- To investigate the component dynamics in asymmetric binary glass formers.
- To analyze the dielectric spectra and relaxation behavior of high-Tg and low-Tg components.
Main Methods:
- Dielectric spectroscopy was used to measure the dielectric spectra of m-tricresyl phosphate and quinaldine mixed with toluene.
- A generalized Cole-Davidson (CD) function was applied to analyze the broadened spectra.
- Stimulated echo experiments and NMR relaxation data were used to confirm findings.
Main Results:
- Broadened spectra could not be described by standard Kohlrausch or CD functions, necessitating a generalized CD function.
- Increasing toluene concentration led to common spectral broadening and failure of frequency-temperature superposition.
- The high-Tg component showed atypical weak relaxation broadening, while the low-Tg component displayed pronounced dynamic heterogeneities.
Conclusions:
- A universal evolution of dynamics for both high-Tg and low-Tg components is suggested for mixtures with high Tg contrast.
- Isodynamic points revealed different concentration dependencies and time scales for each component.
- The study highlights significant dynamic heterogeneities in the faster-relaxing low-Tg component.

