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Density Scaling in Ionic Glass Formers Controlled by Grotthuss Conduction
Author(s) -
Ż. Wojnarowska,
Lidia Tajber,
Marian Paluch
Publication year - 2019
Publication title -
the journal of physical chemistry b
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.864
H-Index - 392
eISSN - 1520-6106
pISSN - 1520-5207
DOI - 10.1021/acs.jpcb.8b09396
Subject(s) - supercooling , scaling , glass transition , amorphous solid , thermodynamics , ionic conductivity , isobaric process , relaxation (psychology) , ionic bonding , materials science , chemistry , condensed matter physics , ion , nuclear magnetic resonance , physics , crystallography , polymer , geometry , mathematics , organic chemistry , psychology , social psychology , electrode , electrolyte
We present investigations of the charge transport in an ionic glass-former carvedilol dihydrogen phosphate (CP) at various T- P- V thermodynamic conditions in terms of density scaling concept. The studied material was found to reveal superprotonic properties both at ambient and elevated pressure, as proved by the Walden rule. Surprisingly, from the isobaric conductivity data, the relaxation times τ σ presented in volume formalism showed no visual evidence of a liquid-glass transition. The different behavior of relaxation dynamics above and below T g was only revealed from the analysis of log τ σ ( V sp ) data at isochronal conditions. The τ σ experimental data of CP plotted as a function of ( TV γ ) -1 satisfy the thermodynamic scaling criterion in the supercooled liquid as well as in the amorphous regime, however with a different γ coefficient (γ SL = 1.12; γ G = 0.48). Nevertheless, by introducing the idea of fictive temperature T f , the transport properties of glassy and supercooled Grotthuss-type conductors measured at various T- P points obey the universal scaling with the use of a single γ parameter.

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