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Register a new userAcoustic attenuation in glasses and its relation with the boson peak
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A theory for the vibrational dynamics in disordered solids [W. Schirmacher, Europhys. Lett. {bf 73}, 892 (2006)], based on the random spatial variation of the shear modulus, has been applied to determine the wavevector ($k$) dependence of the Brillouin peak position ($Omega_k)$ and width ($Gamma_k$), as well as the density of vibrational states ($g(omega)$), in disordered systems. As a result, we give a firm theoretical ground to the ubiquitous $k^2$ dependence of $Gamma_k$ observed in glasses. Moreover, we derive a quantitative relation between the excess of the density of states (the boson peak) and $Gamma_k$, two quantities that were not considered related before. The successful comparison of this relation with the outcome of experiments and numerical simulations gives further support to the theory.
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Experimental results on the density of states and on the acoustic modes of glasses in the THz region are compared to the predictions of two categories of models. A recent one, solely based on an elastic instability, does not account for most observations. Good agreement without adjustable parameters is obtained with models including the existence of non-acoustic vibrational modes at THz frequency, providing in many cases a comprehensive picture for a range of glass anomalies.
We show that a {em vibrational instability} of the spectrum of weakly interacting quasi-local harmonic modes creates the maximum in the inelastic scattering intensity in glasses, the Boson peak. The instability, limited by anharmonicity, causes a complete reconstruction of the vibrational density of states (DOS) below some frequency $omega_c$, proportional to the strength of interaction. The DOS of the new {em harmonic modes} is independent of the actual value of the anharmonicity. It is a universal function of frequency depending on a single parameter -- the Boson peak frequency, $omega_b$ which is a function of interaction strength. The excess of the DOS over the Debye value is $proptoomega^4$ at low frequencies and linear in $omega$ in the interval $omega_b ll omega ll omega_c$. Our results are in an excellent agreement with recent experimental studies.
The inelastic scattering intensities of glasses and amorphous materials has a maximum at a low frequency, the so called Boson peak. Under applied hydrostatic pressure, $P$, the Boson peak frequency, $omega_{rm b}$, is shifted upwards. We have shown previously that the Boson peak is created as a result of a vibrational instability due to the interaction of harmonic quasi localized vibrations (QLV). Applying pressure one exerts forces on the QLV. These shift the low frequency part of the excess spectrum to higher frequencies. For low pressures we find a shift of the Boson peak linear in $P$, whereas for high pressures the shift is $propto P^{1/3}$. Our analytics is supported by simulation. The results are in agreement with the existing experiments.
The boson peak in metallic glasses is modeled in terms of local structural shear rearrangements. Using Eshelbys solution of the corresponding elasticity theory problem (J. D. Eshelby, Proc. Roy. Soc. A241, 376 (1957)), one can calculate the saddle point energy of such a structural rearrangement. The neighbourhood of the saddle point gives rise to soft resonant vibrational modes. One can calculate their density, their kinetic energy, their fourth order potential term and their coupling to longitudinal and transverse sound waves.
New temperature dependent inelastic x-ray (IXS) and Raman (RS) scattering data are compared to each other and with existing inelastic neutron scattering data in vitreous silica (v-SiO_2), in the 300 - 1775 K region. The IXS data show collective propagating excitations up to Q=3.5 nm^-1. The temperature behaviour of the excitations at Q=1.6 nm^-1 matches that of the boson peak found in INS and RS. This supports the acoustic origin of the excess of vibrational states giving rise to the boson peak in this glass.
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