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000033392 0247_ $$2DOI$$a10.1103/PhysRevB.63.104203
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000033392 084__ $$2WoS$$aPhysics, Condensed Matter
000033392 1001_ $$0P:(DE-Juel1)VDB4175$$aBuchenau, U.$$b0$$uFZJ
000033392 245__ $$aMechanical relaxation in glasses and the glass transition
000033392 260__ $$aCollege Park, Md.$$bAPS$$c2001
000033392 300__ $$a104203
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000033392 440_0 $$04919$$aPhysical Review B$$v63$$x1098-0121
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000033392 520__ $$aThe Gilroy-Phillips model of relaxational jumps in asymmetric double-well potentials, developed for the Arrhenius-type secondary relaxations of the glass phase, is extended to a formal description of the breakdown of the shear modulus at the glass transition, the alpha process. The extension requires the introduction of two separate parts of the barrier distribution function f(V), with a different temperature behavior of primary and secondary parts, respectively. The time-temperature scaling of the cu process, together with a sum rule for the whole barrier distribution function, implies a strong rise of the integrated secondary relaxation with increasing temperature above the glass transition. Thus one gets a quantitative relation between the fragility of the glass former and the fast rise of the picosecond process observed in neutron and Raman scattering. The formalism is applied to literature data of polystyrene, vitreous silica and a sodium silicate glass. In the glass phase of polystyrene, one finds a temperature-independent secondary barrier distribution function, in agreement with an earlier Raman result from the literature. Above the glass transition, the secondary barrier distribution function increases with temperature as predicted. The findings allow for an interpretation of the fragility and the entropy crisis at the glass transition.
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