Thomas Blochowicz

Nonresonant dielectric hole burning in neat and binary organic glass formers

Binary mixtures of the molecular glass former 2-picoline in oligostyrene, in which the dielectric response of 2-picoline exhibits a particularly broad distribution of correlation times, are investigated by nonresonant dielectric hole-burning (NDHB) spectroscopy and the results are compared with NDHB in neat systems, in particular, glycerol. It turns out that in both substance classes spectral selectivity is achieved, which indicates that dynamics is heterogeneous, i.e., slow and fast responses coexist in the material. However, in binary systems the position of the spectral modifications is completely determined by the spectral density of the pump field, and thus shifts linearly with burn frequency as expected, also at pump frequencies around the alpha-relaxation maximum. It is shown that in binary systems the lifetime tau(rec) of the spectral modifications is determined by the burn frequency omega(p) and exceeds its inverse by about one order of magnitude, indicating long-lived dynamic heterogeneity. The data are described in terms of a previously suggested model of dynamically selective heating, which was extended to include intrinsic nonexponential relaxation. It turns out that the spectral broadening in binary mixtures is not only due to pronounced dynamic heterogeneity, but partially also due to intrinsic broadening of the relaxation function.

Two Glass Transitions and Secondary Relaxations of Methyltetrahydrofuran in a Binary Mixture

We investigate the molecular dynamics in the binary glass forming system methyltetrahydrofuran (M-THF) and tristyrene. Although the components are miscible in the full concentration and temperature range, two glass transitions can clearly be distinguished in differential scanning calorimetry. We selectively probe the reorientational dynamics of M-THF and tristyrene by means of dielectric spectroscopy and depolarized dynamic light scattering, respectively. While, apart from the observed plasticizer effect, the motion of the larger molecules remains almost unchanged, it is shown that the smaller M-THF molecules take part in both glass transitions. Moreover, below the upper T(g) of the mixture, the remaining mobile M-THF molecules clearly show confinement effects in their relaxation behavior. In order to elucidate the nature of the observed secondary relaxation processes, we first characterize the influence of the methyl group of M-THF on the dynamics in the mixtures by comparing the results obtained so far with the relaxation behavior observed in blends of THF and tristyrene. Finally, we employ (2)H NMR spectroscopy to clarify the nature of the secondary relaxations of THF-d(8) in the latter mixtures and conclude on the basis of the NMR and dielectric results that the high-frequency wing observed in neat M-THF appears as a genuine Johari-Goldstein β-relaxation in the mixtures, whereas the faster secondary process is due to internal degrees of freedom of the nonrigid THF ring.

Concentration fluctuations in a binary glass former investigated by x-ray photon correlation spectroscopy

We investigate structure and dynamics of concentration fluctuations in the binary glass former methyl-tetrahydrofuran and oligomeric methyl metacrylate by photon correlation spectroscopy with partially coherent x-rays from a synchrotron source. Although the system is macroscopically well miscible and optically clear in the full temperature range, calorimetric and dielectric measurements reveal two distinct glass transition temperatures. The relaxation of long range concentration fluctuations turns out to be diffusive and exponential only well above the upper glass transition temperature. As the characteristic time tau(cf) for concentration fluctuations shows a much weaker temperature dependence than the alpha-relaxation both traces finally intersect upon lowering the temperature. Thus, close to T(g), the concentration fluctuations show pronounced features of out-of-equilibrium dynamics such as compressed relaxation functions and a crossover to a ballistic wave vector dependence of tau(cf), like previously observed in various soft matter systems. Moreover, the analysis of time-resolved correlation functions reveals that the relaxation of concentration fluctuations around T(g) involves pronounced dynamic heterogeneities.

Dynamics of water-alcohol mixtures: Insights from nuclear magnetic resonance, broadband dielectric spectroscopy, and triplet solvation dynamics

We combine (2)H nuclear magnetic resonance (NMR), broadband dielectric spectroscopy (BDS), and triplet solvation dynamics (TSD) to investigate molecular dynamics in glass-forming mixtures of water and propylene glycol in very broad time and temperature ranges. All methods yield consistent results for the α process of the studied mixtures, which hardly depends on the composition and shows Vogel-Fulcher temperature dependence as well as Cole-Davidson spectral shape. The good agreement between BDS and TDS data reveals that preferential solvation of dye molecules in microheterogeneous mixtures does not play an important role. Below the glass transition temperature T(g), NMR and BDS studies reveal that the β process of the mixtures shows correlation times, which depend on the water concentration, but exhibit a common temperature dependence, obeying an Arrhenius law with an activation energy of E(a) = 0.54 eV, as previously reported for mixtures of water with various molecular species. Detailed comparison of NMR and BDS correlation functions for the β process unravels that the former decay faster and more stretched than the latter. Moreover, the present NMR data imply that propylene glycol participates in the β process and, hence, it is not a pure water process, and that the mechanism for molecular dynamics underlying the β process differs in mixtures of water with small and large molecules.

Compressed exponential decays in correlation experiments: The influence of temperature gradients and convection

In a wide range of soft materials, correlation experiments using laser light or partially coherent X-rays report the so called compressed exponential correlation functions, i. e., decays c(t) ∝ exp(-(t/τ)(β)) with β > 1. In many cases, this is related to the relaxation of inner stresses, but in some systems, the source of such a phenomenon is still poorly understood. We performed multi speckle-dynamic light scattering experiments in a system of polystyrene spheres in supercooled propanediol. At low temperatures, compressed exponential decays are observed in a multispeckle experiment, in agreement with the literature findings in similar systems. At the same time, due to the particular geometry of our setup, the speckle pattern shows indication for convection in the sample due to a slight temperature gradient across the sample cuvette mounted in a cold finger cryostat. These effects increase with decreasing temperature and after a temperature jump. In some cases it can be corrected for by assuming convective flow at constant velocity. Such corrections reduce or remove compressed exponential behavior in our experiment.

Density and confinement effects of glass forming m-toluidine in nanoporous Vycor investigated by depolarized dynamic light scattering

We investigate the reorientational dynamics of supercooled m-toluidine contained in a matrix of nanoporous Vycor with depolarized dynamic light scattering. Under equilibrium conditions a clear sample is obtained and the dynamics of m-toluidine molecules from inside the nanopores can be accessed via light scattering. However, when supercooling the imbibed liquid at conventional cooling rates, strong non-equilibrium effects occur due to the mismatch of expansion coefficients and the sample gets turbid several tens of Kelvin above the bulk glass transition. Only at cooling rates as low as 0.02 K/min this can be avoided and the dynamics of m-toluidine in confinement can be followed even below the bulk glass transition temperature. In confinement a pronounced acceleration of the reorientational dynamics is observed and the characteristic correlation times follow an Arrhenius law close to T(g). However it seems likely that part of the observed differences to bulk behavior is due to density effects, which are reduced but cannot be fully avoided at low cooling rates.

Debye-Process and β-Relaxation in 1-Propanol Probed by Dielectric Spectroscopy and Depolarized Dynamic Light Scattering

We revisit the reorientational dynamics of 1-propanol as a prototype of a monohydroxy alcohol and H-bonding system by dielectric spectroscopy (DS) and depolarized dynamic light scattering (DDLS). In particular, we address the question of whether the Debye relaxation, which is seen as a dominant process in DS, is visible in light scattering and discuss how the Johari-Goldstein (JG) β-process, which is also a prominent feature of the dielectric spectrum, appears in photon correlation spectroscopy. For that purpose we performed depolarized photon correlation experiments with an improved setup and performed additional time domain dielectric experiments which gives us the possibility to compare dielectric and light scattering data in a broad temperature range. It turns out that the improved setup allows to unambiguously identify the JG β-process, which shows almost identical properties in DDLS as in the dielectric spectra, but a Debye relaxation is not present in the DDLS data and can be excluded down to a level of 2.5% of the α-process amplitude.

Glycerol in micellar confinement with tunable rigidity

We investigate the glassy dynamics of glycerol in the confinement of a microemulsion system, which is stable on cooling down to the glass transition of its components. By changing the composition, we vary the viscosity of the matrix, while keeping the confining geometry intact, as is demonstrated by small angle X-ray scattering. By means of 2H NMR, differential scanning calorimetry, and triplet solvation dynamics we, thus, probe the dynamics of glycerol in confinements of varying rigidity. 2H NMR results show that, at higher temperatures, the dynamics of confined glycerol is unchanged compared to bulk behavior, while the reorientation of glycerol molecules becomes significantly faster than in the bulk in the deeply supercooled regime. However, comparison of different 2H NMR findings with data from calorimetry and solvation dynamics reveals that this acceleration is not due to the changed structural relaxation of glycerol, but rather due to the rotational motion of essentially rigid glycerol droplets or of aggregates of such droplets in a more fluid matrix. Thus, independent of the matrix mobility, the glycerol dynamics remains unchanged except for the smallest droplets, where an increase of Tg and, thus, a slowdown of the structural relaxation is observed even in a fluid matrix.

Triplet Solvation Dynamics of Hydrogen Bonding Liquids in Confinement

Abstract We have developed a flexible experimental setup to conduct triplet solvation dynamics (TSD) experiments. The setup is capable of exciting dyes at 355, 320 and 266 nm. Phosphorescence spectra can be recorded up to a 10 ns-resolution usually covering three decades using a grating spectrograph and a CCD camera. In this contribution, we describe the experimental setup as well as first investigations on water-alcohol mixtures, microemulsions and new dyes for TSD, i.e. naphthalene derivates, which take full advantage of this experimental method sensitive to the local environment of the dyes.