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U. Schneider

Publications and source records attributed to U. Schneider.

24 records · Page 2Linked to original sources
arXiv1999

Propylene Carbonate Reexamined: Mode-Coupling $β$ Scaling without Factorisation ?

The dynamic susceptibility of propylene carbonate in the moderately viscous regime above $T_{\rm c}$ is reinvestigated by incoherent neutron and depolarised light scattering, and compared to dielectric loss and solvation response. Depending on the strength of $α$ relaxation, a more or less extended $β$ scaling regime is found. Mode-coupling fits yield consistently $λ=0.72$ and $T_{\rm c}=182 $K, although different positions of the susceptibility minimum indicate that not all observables have reached the universal asymptotics.

cond-mat.soft↗
arXiv1999

Wide range dielectric spectroscopy on glass-forming materials: an experimental overview

Dielectric spectroscopy is one of the most commonly used techniques for the investigation of the dynamic response of glass-forming materials. The tremendous slow-down of the particle motions when approaching the glass transition and especially the fast processes in glass-forming materials, which have come into the focus of scientific interest recently, make the investigation in a wide frequency range highly desirable. Recently, results from broadband dielectric spectroscopy on glass-forming materials in their liquid and supercooled-liquid state, covering more than 18 decades of frequency have been reported by our group. In the present paper, we give an overview of the various experimental setups and techniques used to collect these spectra. As an example, spectra of the prototypical glass former glycerol are presented.

cond-mat.dis-nn↗
arXiv1999

Linear and non-linear dielectric spectroscopy on ammonium doped Rochelle salt

In this work we present a thorough investigation of the mixed system of Rochelle salt doped with ammonium, with 0<=x<=1 for [Na(K{1-x}(NH4)x)C4H4O6 * 4H2O]. This interesting system is known to exhibit a rich phase diagram with a variety of polar and non-polar phases. However, most of the earlier investigations date back many decades and the experimental advances made since then should enable new insight into the physical nature of its phase diagram. We studied single crystals of 18 doping concentrations using linear and non-linear frequency-dependent dielectric response spectroscopy. In the low field measurements a variety of relaxation features are detected and analyzed in detail. The results for two concentrations of x=0 and x=0.15 are described qualitatively with a simple model. Possibly the most important outcome of the present work is the detection of a new electrically ordered phase for concentrations 0.18<x<0.89.

cond-mat.mtrl-sci↗
arXiv1998

Broadband dielectric response of glycerol and propylene carbonate: a comparison

Dielectric data on glycerol and propylene carbonate covering 18 decades of frequency are presented and compared to each other. Both materials exhibit qualitatively similar behavior except for marked differences in the high-frequency region just below the boson peak. The results on both materials are consistent with the mode coupling theory of the glass transition.

cond-mat.dis-nn↗
arXiv1998

Broadband Dielectric Spectroscopy on Glass-Forming Propylene Carbonate

Dielectric spectroscopy covering more than 18 decades of frequency has been performed on propylene carbonate in its liquid and supercooled-liquid state. Using quasi-optic submillimeter and far-infrared spectroscopy the dielectric response was investigated up to frequencies well into the microscopic regime. We discuss the alpha-process whose characteristic timescale is observed over 14 decades of frequency and the excess wing showing up at frequencies some three decades above the peak frequency. Special attention is given to the high-frequency response of the dielectric loss in the crossover regime between alpha-peak and boson-peak. Similar to our previous results in other glass forming materials we find evidence for additional processes in the crossover regime. However, significant differences concerning the spectral form at high frequencies are found. We compare our results to the susceptibilities obtained from light scattering and to the predictions of various models of the glass transition.

cond-mat.dis-nn↗