Nuclear-Magnetic-Resonance Measurements Reveal the Origin of the Debye Process in Monohydroxy Alcohols

C. Gainaru, R. Meier, S. Schildmann, C. Lederle, W. Hiller, E. A. Rössler, and R. Böhmer
Phys. Rev. Lett. 105, 258303 – Published 16 December 2010

Abstract

Monohydroxy alcohols show a structural relaxation and at longer time scales a Debye-type dielectric peak. From spin-lattice relaxation experiments using different nuclear probes, an intermediate, slower-than-structural dynamics is identified for n-butanol. Based on these findings and on translational diffusion measurements, a model of self-restructuring, transient chains is proposed. The model is demonstrated to explain consistently the so-far puzzling observations made for this class of hydrogen-bonded glass forming liquids.

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  • Received 25 August 2010

DOI:https://doi.org/10.1103/PhysRevLett.105.258303

© 2010 The American Physical Society

Authors & Affiliations

C. Gainaru1,*, R. Meier2, S. Schildmann1, C. Lederle1, W. Hiller3, E. A. Rössler2, and R. Böhmer1,†

  • 1Fakultät für Physik, Technische Universität Dortmund, 44221 Dortmund, Germany
  • 2Physikalisches Institut, Universität Bayreuth, 95440 Bayreuth, Germany
  • 3Fakultät für Chemie, Technische Universität Dortmund, 44221 Dortmund, Germany

  • *catalin.gainaru@tu-dortmund.de
  • roland.bohmer@tu-dortmund.de

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Vol. 105, Iss. 25 — 17 December 2010

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