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Non-polymeric asymmetric binary glass-formers. II. Secondary relaxation studied by dielectric, ²H NMR, and 31P NMR spectroscopy.

Authors :
Pötzschner, B.
Mohamed, F.
Bacher, C.
Wagner, E.
Lichtinger, A.
Bock, D.
Kreger, K.
Schmidt, H.-W.
Rössler, E. A.
Source :
Journal of Chemical Physics; 2017, Vol. 146 Issue 16, p1-10, 10p, 1 Diagram, 11 Graphs
Publication Year :
2017

Abstract

We investigate the secondary (β-) relaxations of an asymmetric binary glass former consisting of a spirobichroman derivative (SBC; T<subscript>g</subscript> = 356 K) as the high-T<subscript>g</subscript> component and the low-T<subscript>g</subscript> component tripropyl phosphate (TPP; T<subscript>g</subscript> = 134 K). The main relaxations are studied in Paper I [B. Potzschner et al., J. Chem. Phys. 146, 164503 (2017)]. A high T<subscript>g</subscript> contrast of ΔT<subscript>g</subscript> = 222 K is put into effect in a non-polymeric system. Component-selective studies are carried out by combining results from dielectric spectroscopy (DS) for mass concentrations c<subscript>TPP</subscript> ≤ 60% and those from different methods of 2H and <subscript>31</subscript>P NMR spectroscopy. In the case of NMR, the full concentration range (10% ≤ c<subscript>TPP</subscript> ≤ 100%) is covered. The neat components exhibit β-relaxation (β <subscript>1</subscript> (SBC) and β <subscript>2</subscript> (TPP)). The latter is rediscovered by DS in the mixtures for all concentrations with unchanged time constants. NMR spectroscopy identifies the β-relaxations as being alike to those in neat glasses. A spatially highly restricted motion with angular displacement below ±10° encompassing all molecules is involved. In the lowtemperature range, where TPP shows the typical 31PNMRecho spectra of the <subscript>α2</subscript>-process, very similar spectral features are observed for the (deuterated) SBC component by 2H NMR, in addition to its "own" β <subscript>1</subscript>-process observed at high temperatures. Apparently, the small TPP molecules enslave the large SBC molecules to perform a common hindered reorientation. The temperature dependence of the spin-lattice relaxation time of both components is the same and reveals an angular displacement of the SBC molecules somewhat smaller than that of TPP, though the time constants τ<subscript>β2</subscript> are the same. Furthermore, T<subscript>1</subscript> (T) of TPP in the temperature region of the β <subscript>2</subscript>-process is absolutely the same as in the mixture TPP/polystyrene investigated previously. It appears that the manifestations of the β-process introduced by one component are essentially independent of the second component. Finally, at c<subscript>TPP</subscript> ≤ 20% one finds indications that the β <subscript>2</subscript>-process starts to disintegrate. More and more TPP molecules get immobilized upon decreasing c<subscript>TPP</subscript>. We conclude that the β-process is a cooperative process. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00219606
Volume :
146
Issue :
16
Database :
Complementary Index
Journal :
Journal of Chemical Physics
Publication Type :
Academic Journal
Accession number :
122804274
Full Text :
https://doi.org/10.1063/1.4980085