Sound waves and other modes in the strong glass former B2O3

D. Engberg, A. Wischnewski, U. Buchenau, L. Börjesson, A. J. Dianoux, A. P. Sokolov, and L. M. Torell
Phys. Rev. B 58, 9087 – Published 1 October 1998
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Abstract

We have investigated fast relaxational processes and the much debated boson peak in the strong glass former, B2O3, from 60 to 1300 K (glass transition temperature 523 K) using coherent inelastic neutron scattering. The wave-vector dependence of the dynamic structure factor is different for energies below and above the boson peak, at 2.5meV, indicating a qualitative difference in the character of the respective modes. This finding demonstrates that the boson peak can be decomposed into an in-phase and a random-phase component. A quantitative analysis to separate these contributions has been carried out. At low temperatures the in-phase component extrapolates to the Debye level at low frequencies. It is then identified with the sound-wave contribution. At higher frequencies it increases to a maximum value at 2meV and then the value decreases and becomes less than the Debye level at 4meV. The density of states for the random-phase component reaches a maximum value at 3meV and is similar to the boson peak observed in Raman scattering. The low-frequency behavior of the random-phase modes as well as the higher-frequency behavior of the total density of states are consistent with predictions of the soft potential model. At temperatures above the glass transition temperature we observe, in accordance with other glass formers, a strongly anharmonic behavior of the spectra. However for T800K the system exhibits harmoniclike behavior and the dynamical properties of the system are essentially temperature independent up to the highest temperature of observation, an extraordinary finding.

  • Received 6 August 1997

DOI:https://doi.org/10.1103/PhysRevB.58.9087

©1998 American Physical Society

Authors & Affiliations

D. Engberg*

  • Department of Physics, Chalmers Unveristy of Technology, S-412 96 Göteborg, Sweden

A. Wischnewski and U. Buchenau

  • Institut für Festkörperforschung, Forschungszentrum Jülich Postfach 1913, D-52425 Jülich, Federal Republic of Germany

L. Börjesson

  • Department of Applied Physics, Chalmers University of Technology, S-412 96 Göteborg, Sweden

A. J. Dianoux

  • Institut Laue-Langevin, BP 156, F-38042 Grenoble Cedex 9, France

A. P. Sokolov

  • Institut für Festkörperforschung, Forschungszentrum Jülich Postfach 1913, D-52425 Jülich, Federal Republic of Germany

L. M. Torell

  • Department of Physics, Chalmers University of Technology, S-412 96 Göteborg, Sweden

  • *Present address: Rutherford-Appleton Laboratory, Chilton, Didcot, Oxon OX11 0QX, United Kingdom.

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Issue

Vol. 58, Iss. 14 — 1 October 1998

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