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Coupling and decoupling of molecular reorientation and charge transport in Li-salt-doped cycloalcohol ion conductors

  • Using broadband impedance spectroscopy and conductometry, we study the phase behavior and the reorientational and translational dynamics of cycloalcohols doped with 1 to 20 mol% of Li salt. At low salt concentrations, a plastically crystalline state is stable. In this regime, the dielectric spectra of the cycloalcohols reveal two relaxation processes. One of them originates from the α-relaxation and indicates an orientational glass transition. The other, much slower process, is related to ionic hopping. By comparing reorientation times with electrical conductivities, for 1 mol% Li doping, previous studies suggested an only weak decoupling of rotational and translational motions. Rather than analyzing disparate quantities, the present work directly compares peak frequencies corresponding to reorientational and translational rates. This approach allows one to resolve the mild, yet significant divergence of the two rates, i.e., a dynamic decoupling, also for higher doping levels and forUsing broadband impedance spectroscopy and conductometry, we study the phase behavior and the reorientational and translational dynamics of cycloalcohols doped with 1 to 20 mol% of Li salt. At low salt concentrations, a plastically crystalline state is stable. In this regime, the dielectric spectra of the cycloalcohols reveal two relaxation processes. One of them originates from the α-relaxation and indicates an orientational glass transition. The other, much slower process, is related to ionic hopping. By comparing reorientation times with electrical conductivities, for 1 mol% Li doping, previous studies suggested an only weak decoupling of rotational and translational motions. Rather than analyzing disparate quantities, the present work directly compares peak frequencies corresponding to reorientational and translational rates. This approach allows one to resolve the mild, yet significant divergence of the two rates, i.e., a dynamic decoupling, also for higher doping levels and for different Li salts. The electrolytes that form at Li salt concentrations of 5 mol% and more display a qualitatively different behavior. In this compositional regime, a liquid-to-glass transition arises and the ion hopping time that we probe using lithium nuclear magnetic resonance and proton-detected diffusometry is compatible with the reorientational time scales. This observation implies a close coupling of both underlying degrees of freedom.show moreshow less

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Metadaten
Author:Sofiane Lansab, Yannik Hinz, Bastian Grabe, Peter LunkenheimerORCiDGND, Roland Böhmer
URN:urn:nbn:de:bvb:384-opus4-1239021
Frontdoor URLhttps://opus.bibliothek.uni-augsburg.de/opus4/123902
ISSN:1463-9076OPAC
ISSN:1463-9084OPAC
Parent Title (English):Physical Chemistry Chemical Physics
Publisher:Royal Society of Chemistry (RSC)
Place of publication:London
Type:Article
Language:English
Year of first Publication:2025
Publishing Institution:Universität Augsburg
Release Date:2025/07/28
Volume:27
Issue:30
First Page:16161
Last Page:16171
DOI:https://doi.org/10.1039/d5cp02003d
Institutes:Mathematisch-Naturwissenschaftlich-Technische Fakultät
Mathematisch-Naturwissenschaftlich-Technische Fakultät / Institut für Physik
Mathematisch-Naturwissenschaftlich-Technische Fakultät / Institut für Physik / Lehrstuhl für Experimentalphysik V
Dewey Decimal Classification:5 Naturwissenschaften und Mathematik / 53 Physik / 530 Physik
Licence (German):CC-BY 3.0: Creative Commons - Namensnennung (mit Print on Demand)