Low-temperature specific heat measurements have been performed in porous silica xerogels with densities varying from 670 to 1730 kg m−3 to study the low-energy vibrational dynamics. The specific heat, Cp, shows a bump in the temperature range above 4 K, when reported in a plot of Cp/T3 against the temperature, T. The bump is almost independent of the sample density and is close to the boson peak observed in melt-quenched amorphous silica (a-SiO2). At temperatures <4 K, an additional contribution to that predicted by the Debye theory is observed. It follows an approximately linear temperature dependence (Cexc=aT1+v, v being equal to about 0.25). In the xerogel with the largest density, specific heat of about a factor 5 larger than that of a-SiO2 is measured, which increases with decreasing sample density. By comparison with the corresponding properties of a-SiO2, we conclude that the disorder introduced by the presence of pores does not measurably affect the excess density of vibrational states in a frequency range of the boson peak (BP), but increases the density of the two-level systems (TLS).

Low-temperature specific heats of porous silica xerogels of low densities

D'ANGELO, Giovanna;TRIPODO, Gaspare;CARINI, Giuseppe;
2001-01-01

Abstract

Low-temperature specific heat measurements have been performed in porous silica xerogels with densities varying from 670 to 1730 kg m−3 to study the low-energy vibrational dynamics. The specific heat, Cp, shows a bump in the temperature range above 4 K, when reported in a plot of Cp/T3 against the temperature, T. The bump is almost independent of the sample density and is close to the boson peak observed in melt-quenched amorphous silica (a-SiO2). At temperatures <4 K, an additional contribution to that predicted by the Debye theory is observed. It follows an approximately linear temperature dependence (Cexc=aT1+v, v being equal to about 0.25). In the xerogel with the largest density, specific heat of about a factor 5 larger than that of a-SiO2 is measured, which increases with decreasing sample density. By comparison with the corresponding properties of a-SiO2, we conclude that the disorder introduced by the presence of pores does not measurably affect the excess density of vibrational states in a frequency range of the boson peak (BP), but increases the density of the two-level systems (TLS).
2001
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11570/2165221
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