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Sound absorption in glasses

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 Added by Uli Buchenau
 Publication date 2020
  fields Physics
and research's language is English
 Authors U. Buchenau




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The paper presents a description of the sound wave absorption in glasses, from the lowest temperatures up to the glass transition, in terms of two compatible phenomenological models. Resonant tunneling, the rise of the relaxational tunneling to the tunneling plateau and the crossover to classical relaxation are universal features of glasses and are well described by the extension of the tunneling model to include soft vibrations and low barrier relaxations, the soft potential model. Its further extension to non-universal features at higher temperatures is the very flexible Gilroy-Phillips model, which allows to determine the barrier density of the energy landscape of the specific glass from the frequency and temperature dependence of the sound wave absorption in the classical relaxation domain. To apply it properly at elevated temperatures, one needs its formulation in terms of the shear compliance. As one approaches the glass transition, universality sets in again with an exponential rise of the barrier density reflecting the frozen fast Kohlrausch t^beta-tail (in time t, with beta close to 1/2) of the viscous flow at the glass temperature. The validity of the scheme is checked for literature data of several glasses and polymers with and without secondary relaxation peaks. The frozen Kohlrausch tail of the mechanical relaxation shows no indication of the strongly temperature-dependent excess wing observed in dielectric data of molecular glasses with hydrogen bonds. Instead, the mechanical relaxation data indicate an energy landscape describable with a frozen temperature-independent barrier density for any glass.



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84 - Lijin Wang , Elijah Flenner , 2020
The temperature dependence of the thermal conductivity of amorphous solids is markedly different from that of their crystalline counterparts, but exhibits universal behaviour. Sound attenuation is believed to be related to this universal behaviour. Recent computer simulations demonstrated that in the harmonic approximation sound attenuation $Gamma$ obeys quartic, Rayleigh scattering scaling for small wavevectors $k$ and quadratic scaling for wavevectors above the Ioffe-Regel limit. However, simulations and experiments do not provide a clear picture of what to expect at finite temperatures where anharmonic effects become relevant. Here we study sound attenuation at finite temperatures for model glasses of various stability, from unstable glasses that exhibit rapid aging to glasses whose stability is equal to those created in laboratory experiments. We find several scaling laws depending on the temperature and stability of the glass. First, we find the large wavevector quadratic scaling to be unchanged at all temperatures. Second, we find that at small wavectors $Gamma sim k^{1.5}$ for an aging glass, but $Gamma sim k^2$ when the glass does not age on the timescale of the calculation. For our most stable glass, we find that $Gamma sim k^2$ at small wavevectors, then a crossover to Rayleigh scattering scaling $Gamma sim k^4$, followed by another crossover to the quadratic scaling at large wavevectors. Our computational observation of this quadratic behavior reconciles simulation, theory and experiment, and will advance the understanding of the temperature dependence of thermal conductivity of glasses.
Three classes of harmonic disorder systems (Lennard-Jones like glasses, percolators above threshold, and spring disordered lattices) have been numerically investigated in order to clarify the effect of different types of disorder on the mechanism of high frequency sound attenuation. We introduce the concept of frustration in structural glasses as a measure of the internal stress, and find a strong correlation between the degree of frustration and the exponent alpha that characterizes the momentum dependence of the sound attenuation $Gamma(Q)$$simeq$$Q^alpha$. In particular, alpha decreases from about d+1 in low-frustration systems (where d is the spectral dimension), to about 2 for high frustration systems like the realistic glasses examined.
132 - Di Zhou 2016
In low-temperature glasses, the sound velocity changes as the logarithmic function of temperature below $10$K: $[c(T) - c(T_0)]/c(T_0) = mathcal{C}ln(T/T_0)$. With increasing temperature starting from $T=0$K, the sound velocity does not increase monotonically, but reaches a maximum at a few Kelvin and decreases at higher temperatures. Tunneling-two-level-system (TTLS) model explained the $ln T$ dependence of sound velocity shift. In TTLS model the slope ratio of $ln T$ dependence of sound velocity shift between lower temperature increasing regime (resonance regime) and higher temperature decreasing regime (relaxation regime) is $mathcal{C}^{rm res }:mathcal{C}^{rm rel }=1:-frac{1}{2}$. In this paper we develop the generic coupled block model to prove the slope ratio of sound velocity shift between two regimes is $mathcal{C}^{rm res }:mathcal{C}^{rm rel }=1:-1$ rather than $1:-frac{1}{2}$, which agrees with the majority of the measurements. The dielectric constant shift in low-temperature glasses, $[epsilon_r(T)-epsilon_r(T_0)]/epsilon_r(T_0)$, has a similar logarithmic temperature dependence below $10$K: $[epsilon(T)-epsilon(T_0)]/epsilon(T_0) = mathcal{C}ln(T/T_0)$. In TTLS model the slope ratio of dielectric constant shift between resonance and relaxation regimes is $mathcal{C}^{rm res}:mathcal{C}^{rm rel}=-1:frac{1}{2}$. In this paper we apply the electric dipole-dipole interaction, to prove that the slope ratio between two regimes is $mathcal{C}^{rm res}:mathcal{C}^{rm rel} = -1:1$ rather than $-1:frac{1}{2}$. Our result agrees with the dielectric constant measurements. By developing a real space renormalization technique for glass non-elastic and dielectric susceptibilities, we show that these universal properties essentially come from the $1/r^3$ long range interactions, independent of the materials microscopic properties.
Some facets of the way sound waves travel through glasses are still unclear. Recent works have shown that in the low-temperature harmonic limit a crucial role in controlling sound damping is played by local elastic heterogeneity. Sound waves propagation has been demonstrated to be strongly affected by inhomogeneous mechanical features of the materials, which add to the anharmonic couplings at finite temperatures. We describe the interplay between these two effects by molecular dynamics simulation of a model glass. In particular, we focus on the transverse components of the vibrational excitations in terms of dynamic structure factors, and characterize the temperature dependence of sound attenuation rates in an extended frequency range. We provide a complete picture of all phenomena, in terms encompassing both theory and experiments.
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