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Probing the non-Debye low-frequency excitations in glasses through random pinning
Luca Angelani1,2, Matteo Paoluzzi3, Giorgio Parisi4,5,6
1Institute for Complex Systems, National Research Council (ISC-CNR), 00185 Rome, Italy.
Summary
Adding pinned particles to a 3D model glass former reveals emerging soft localized modes. This study shows the low-frequency density of states follows a power law above a critical pinned fraction, impacting vibrational properties.
Area of Science:
- Condensed Matter Physics
- Materials Science
- Statistical Mechanics
Background:
- Understanding the vibrational properties of amorphous materials like glass is crucial.
- The low-frequency spectrum of the density of states (DOS) in glasses deviates from Debye's prediction (non-Debye behavior).
- Localized vibrational modes are key to explaining these non-Debye features.
Purpose of the Study:
- To investigate the emergence and properties of low-frequency vibrational modes in a 3D model glass former.
- To analyze how introducing pinned particles affects the density of states spectrum.
- To characterize the power-law behavior of the low-frequency tail of the DOS.
Main Methods:
- Simulated a 3D model glass former.
- Introduced a random pinning field to freeze a fraction (p) of particles, breaking translational invariance.
- Analyzed the vibrational density of states (DOS) as a function of the pinned particle fraction.
Main Results:
- Non-Debye soft localized modes progressively emerge as the fraction (p) of pinned particles increases.
- The vibrational frequencies of extended modes are shifted to higher frequencies by the pinning field.
- The low-frequency tail of the DOS exhibits power-law decay (g(ω) ~ ω^α) above a critical pinned fraction (p_c).
Conclusions:
- Pinning particles is an effective method to enhance and study non-Debye soft localized modes in glasses.
- The observed power-law behavior in the DOS indicates a transition in the vibrational spectrum.
- These findings contribute to a deeper understanding of vibrational dynamics and localization in amorphous solids.
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